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The absorption of a free-standing ultra-thin film supporting a single resonant mode is, in principle, limited to 50%. Based on the degenerate critical coupling (DCC) of dipole modes, silicon Mie resonators can overcome the absorption limit and achieve perfect absorption in the green light range. DCC requires that the radiative loss of each dipole mode matches material loss. Due to the material properties of silicon, the material loss varies with wavelength. Therefore, flexible tuning of radiative loss to match the wavelength-dependent material loss is crucial for realizing DCC-based perfect absorbers. In this study, we propose that a 45-degree rotation of cubic Mie resonators enhances the radiative loss of electric dipole mode. Hence, the DCC-based perfect absorption can be extended to the violet light range. In addition to applications in photodetectors and imaging sensor pixels, the proposed perfect absorber has great potential to become nonlinear elements based on the photothermal effect for photonic neuromorphic computing due to its temperature-dependent scattering. [ABSTRACT FROM AUTHOR]

This paper reports on the application of a near-infrared (NIR) imaging system for visualizing heat transfer dynamics from a bulk gadolinium (Gd) sample to the surrounding water during the magnetization/demagnetization process of the magnetocaloric effect (MCE). The suggested approach relied on the spectral variation in water absorption band at 1150 nm wavelength within the NIR spectrum. An experimental setup integrated a telecentric uniform-illumination system, a halogen lamp, and an NIR camera to enable real-time monitoring of a single magnetization and demagnetization cycle induced by an external magnetic field, which was generated by a permanent-magnet-based magnetic circuit. Two-dimensional absorbance images captured during this cycle clearly depicted the thermal energy generated by the MCE in water. Furthermore, an analysis of the thermal boundary layer and the quantification of heat transfer from Gd to water provided insights into the dynamics over time. These results indicated the potential of our NIR imaging techniques in optimizing thermal–fluid interactions within MCE systems, thereby improving the design and efficiency of magnetic refrigeration systems. [ABSTRACT FROM AUTHOR]

We present a basic framework for modeling collective mode effects in photocurrent measurements performed on two-dimensional materials using nano-optical scanned probes. We consider photothermal, photovoltaic, and bolometric contributions to the photocurrent. We show that any one of these can dominate depending on frequency, temperature, applied bias, and sample geometry. Our model is able to account for periodic spatial oscillations (fringes) of the photocurrent observed near sample edges or inhomogeneities. For the case of a non-absorbing substrate, we find a direct relation between the spectra measured by the photocurrent nanoscopy and its parental scanning technique near-field optical microscopy. [ABSTRACT FROM AUTHOR]

In order to solve the problems of low energy utilization and poor structural stability of photothermal conversion materials, a graphene-based photothermal conversion material was prepared, which was structurally integrated with a light-absorbing upper layer and a heat insulating base. During the preparation process, a tightly arranged nanotube array upper layer was constructed on the basis of graphene films by microimprinting technology, and a porous aerogel base was molded by a fixed-point titration and multiple-foaming method. The results show that the light trap constructed from graphene hollow nanotubes can significantly increase the number of light reflections and reduce light reflectivity. Meanwhile, the length of the nanotubes is directly proportional to the light-absorbing capacity of the material, which can increase the light-absorbing rate to more than 98% under the embossing conditions of 85 kN and 8h. In addition, the porous aerogel insulation base can effectively improve the photothermal conversion effect, and a photothermal conversion efficiency of 87% and a water evaporation rate of 1.3 kg/(m2 h) can be achieved at a base thickness of 6 mm. [ABSTRACT FROM AUTHOR]

The development of robust and efficient photocatalytic constructs for boosting the water oxidation reaction (WOR) is needed for establishing a sunlight-driven renewable energy infrastructure. Here, we synthesized plasmonic core–shell nanoconstructs consisting of triangular gold nanoprism (AuTNP) core with mixed manganese oxide (MnOx) shell for photoelectrocatalytic WOR. These constructs show electrocatalytic WOR with a low onset overpotential requirement of 270 mV at pH 10. Photoexcitation showed further enhancement of their catalytic activity resulting in ∼15% decrease of the onset overpotential requirement along with the generation of photocurrent density of up to 300 μA/cm2. We showed that such light-driven enhancement of AuTNP@MnOx dyad's catalytic activity toward the WOR process includes contributions from both photocatalytic (hot carriers driven) and photothermal effects with photothermal effect playing the major role for wavelength between 532 and 808 nm. The contribution from the photocatalytic effect is appreciable only for high-energy excitations near the interband region, while the photothermal effect largely dominates for lower energy excitations near the LSPR wavelengths of the dyad. [ABSTRACT FROM AUTHOR]

Efficient absorption of solar radiation holds the key to photothermal utilization; however, realizing solar absorber designs with high absorption efficiency remains challenging. Herein, a nickel-based metamaterial selective solar absorber with a nanopillar array structure was proposed to realize nearly perfect optical absorption over a broad spectrum. The average absorbance is up to 96% in the 300–2033 nm wavelength range. Notably, a reasonably detailed analysis of the physical mechanism of the proposed absorber was performed in this paper, attributing the exceptional broadband absorption to the concurrent interaction with surface plasmon resonance, quarter-wavelength resonance, and electric dipole resonance. The absorption efficiency declines significantly when λ > 2.5 μm, with only 20% absorptivity at λ = 6 μm in the radiation-absorbing transition region. This decline is desirable, as it contributes to reducing the emissivity in the mid-infrared range and, therefore, prevents self-radiation. The results demonstrate that the selective absorber possesses the potential to capture solar energy within a broadband, while avoiding undesirable self-radiation, thereby enhancing the integral efficiency of the solar energy conversion system. Moreover, the absorption spectrum shows insensitivity to polarization and angle of incidence. The selective solar absorber proposed here offers excellent performance with a simple structure, showing great promise in the field of photothermal conversion. [ABSTRACT FROM AUTHOR]

Time-resolved pump–probe and two-dimensional spectroscopy are widely used to study ultrafast chemical and biological processes in solutions. However, the corresponding signals at long times can be contaminated by molecular photothermal effects, which are caused by the nonradiative heat dissipation of photoexcited molecules to the surroundings. Additionally, molecular diffusion affects the transient spectroscopic signals because photoexcited molecules can diffuse away from the pump and probe beam focuses. Recently, a theoretical description of molecular photothermal effects on time-resolved IR spectroscopy was reported. In this work, I consider the molecular photothermal process, molecular diffusion, and sample flow to develop a generalized theoretical description of time-resolved spectroscopy. The present work can be used to interpret time-resolved spectroscopic signals of electronic or vibrational chromophores and understand the rate and mechanisms of the conversion of high-frequency molecular electronic and vibrational energy to solvent kinetic energy in condensed phases. [ABSTRACT FROM AUTHOR]

Using colloids effectively confined in two dimensions by a cell with a thickness comparable to the particle size, we investigate the nucleation and growth of crystallites induced by locally heating the solvent with a near-infrared laser beam. The particles, which are "thermophilic," move towards the laser spot solely because of thermophoresis with no convection effects, forming dense clusters whose structure is monitored using two order parameters that gauge the local density and the orientational ordering. We find that ordering takes place when the cluster reaches an average surface density that is still below the upper equilibrium limit for the fluid phase of hard disks, meaning that we do not detect any sign of a proper "two-stage" nucleation from a glass or a polymorphic crystal structure. The crystal obtained at late growth stage displays a remarkable uniformity with a negligible amount of defects, arguably because the incoming particles diffuse, bounce, and displace other particles before settling at the crystal interface. This "fluidization" of the outer crystal edge may resemble the surface enhanced mobility giving rise to ultra-stable glasses by physical vapor deposition. [ABSTRACT FROM AUTHOR]

The photocatalytic H 2 production technology exhibits promising potential in addressing the challenges of environmental pollution and energy crisis. In this work, CuS particles decorated MoS 2 seaweed spheres (MoS 2 /CuS) were synthesized through a hydrothermal method, then they are loaded on the surface of g-C 3 N 4 nanosheets using a solvent evaporation strategy to form MoS 2 /CuS/g-C 3 N 4 double S-scheme heterojunction. The investigation reveals the H 2 production rate of 25 wt % MoS 2 /CuS/g-C 3 N 4 can reach up to 1438 μmol·g-1·h-1, which is 14.8-fold of g-C 3 N 4 (97 μmol·g-1·h-1). Further studies indicate that the introduction of MoS 2 /CuS can broaden the light absorption range, increase electrochemical specific surface area, reduce the activation energy for H 2 production and increase hydrophilicity of the composite. Especially, CuS can suppress carrier recombination effectively through its electron storage and release ability. Based on the experimental and theoretical analysis of band structures, the charge transfer in MoS 2 /CuS/g-C 3 N 4 shares optimized double S-scheme charge transfer pathways with a dual reduction site, leading to an enhanced H 2 evolution kinetics. This work offers valuable insights for the advancement of novel double S-scheme heterojunctions, showcasing their potential in energy storage and photothermal enhancement effects. In the MoS 2 /CuS/g-C 3 N 4 double S-scheme heterojunction, the difference of Fermi level facilitates e− transfers from MoS 2 and g-C 3 N 4 to CuS (Cu2+ + e−→ Cu+), enabling CuS to act as an electron reservoir. In addition, oxidized semiconductor (CuS) release e− that recombine with the holes of MoS 2 and g-C 3 N 4. The capacitive properties of the composite, combined with the presence of dual reduction site, can significantly enhance the kinetic reaction for H 2 production. [Display omitted] • MoS 2 /CuS/g-C 3 N 4 double S-scheme is obtained by a solvent evaporation strategy. • Double S-scheme heterojunction can provide two reduction sites for H 2 evolution. • Double S-scheme charge separation route can retain the high reactivity of charges. • The capacitive property of CuS can efficiently hinder the recombination of charges. • MoS 2 /CuS/g-C 3 N 4 exhibits good stability and superior activity for H 2 production. [ABSTRACT FROM AUTHOR]

Vanadium oxide (VO x) has demonstrated significant potential in various applications, including sensors (included but not limited to photodetection), smart windows, and energy storage devices, attributed to its pronounced semiconductor-to-metal transition near 340 K, coupled with a structural transition. However, the requirement for high-temperature synthesis to achieve the desired phases for these applications has limited its broader utilization, particularly in contexts where high temperatures are impractical. Here, we examined the effect of thermal annealing on the structural, electronic, and photodetection properties of VO x / p- Si heterojunctions fabricated via dip coating. VO x films were categorized into three types: pristine (VO x-1), annealed at 300 °C (VO x-2), and 500 °C (VO x-3). X-ray diffraction analysis confirmed hydrated V 2 O 5 in VO 1-x and VO x-2 , while VO x-3 was pure and crystalline V 2 O 5. Significantly, the band gap narrowed from 2.75 eV in VO x-1 to 2.46 eV in VO x-3 , a result attributed to grain growth and the consequential attenuation of quantum confinement effects. The DFT calculations implemented through the VASP code supported these findings, revealing an annealing-induced increase in the work function, revealing enhanced surface electronic properties favourable to photodetection. The electrical properties of the PN heterojunction Ag/ n- VO x / p- Si/Ag with Ag/ n- VO x terminal grounded showed a transition from ohmic-like in VO x-1 to rectifying behaviour for VO x-2 and VO x-3 with dark condition reverse bias current larger than the forward bias current, showing typical Schottky junction type contact between p- Si and n- VO x. This behaviour highlights the role of annealing in modulating the interface properties between p- Si and n- VO x. Notably, the heterojunctions demonstrated superior photodetection across IR, red, green, blue, and UV spectra, with performance metrics like responsivity and sensitivity markedly improved post-annealing, attributed to increased crystallinity and reduced interface traps and work function tuning. Additionally, the devices exhibited rapid transient responses under periodic LED illumination, highlighting their potential for advanced photodetection applications. The study explores the enhancement of photodetector efficiency through thermal annealing of vanadium oxide on p- Si substrates. Annealing at 300 °C and 500 °C leads to significant improvements in crystal structure and electronic properties, confirmed by X-ray diffraction and DFT calculations. The annealed VO x films show a narrowed band gap, higher work function, and transition from ohmic to rectifying behaviour in electrical characteristics. Photodetection metrics like responsivity and sensitivity improve markedly post-annealing, with rapid response times under LED illumination, highlighting the potential for advanced photodetector applications across a broad spectral range. [Display omitted] • Thermal annealing tunes electrical, optical, and structural properties of dip-coated V2O5 on p-Si. • X-ray Diffraction and optical absorption confirm dehydration, crystallization, and bandgap narrowing. • DFT calculations reveal an annealing-induced increase in work function. • Work function tuning enhances photoresponsivity and rapid transient photocurrents across UV–Vis–NIR spectra. • Heterojunctions exhibit superior performance metrics under LED illumination. [ABSTRACT FROM AUTHOR]

In this study, we synthesize pristine and (Mg, Fe) co-doped SnO 2 nanoparticles using the chemical co-precipitation method, where the Mg doping amount is fixed (2 mol%) and the amount of Fe is varied between 2 and 6 mol%. The narrow and sharp natures of intense XRD peaks notify that the crystallinity is pretty well. The formation of the single-phase tetragonal rutile type structure of all prepared compounds has been identified by Rietveld refinement, Fourier-transform infrared spectroscopy (FTIR), and Raman spectroscopy. Moreover, the well incorporation of Fe and Mg in SnO 2 and absence of any other unexpected elements are confirmed by the energy dispersive X-ray spectroscopy. How the co-doping of Mg and Fe alter the crystallite size, microstrain, and dislocation density of the prepared samples have been investigated by Scherrer method with various modified version of it, Williamson-Hall method (W–H) in three factions (UDM, USDM, and UDEDM), Size strain plot (SSP) method, Halder-Wagner (H–W) method, Wagner-Aqua (W-A) method, and Warren-Averbach (WA) method. The obtained crystallite size using the WA method is smaller than the other methods and Scherrer-based methods show much comparable (except SLMSE) sizes. Additionally, the W–H, H–W, SSP, and W-A plots show almost similar tendency of decreasing crystal size, increasing dislocation density and lattice strain with increasing doping. The scanning electron microscopy (SEM) profiles revealed that the synthesized nanoparticles are agglomerated in nature, where the agglomeration increases with decreasing crystal size. The magnetic response of the prepared samples revealed a weak ferromagnetic (or soft magnetic) nature, where saturation magnetization increased due to doping, and a reducing trend of remanent magnetization and coercivity was explored which indicates the phase transition from ferromagnetic to paramagnetic. However, this soft magnetic nature was modified with the influence of defects like changes in lattice parameters, strain, and oxygen vacancy. This phase transition at higher doping concentration makes our nanomaterial as a suitable contender for memory devices, hyperthermia treatment, and photothermal effect. [ABSTRACT FROM AUTHOR]

We present an intelligent photothermal therapy agents by functionalizing gold nanoparticles with specific nucleic acid sequences. Hairpin nucleic acids are modified to the nanoparticles, forming AuNPs-1 and AuNPs-2. Upon infiltrating cancer cells, these nanoparticles undergo catalytic hairpin assembly in the presence of target miRNA, leading to aggregation and subsequent photothermal conversion. Under near-infrared laser irradiation, aggregated gold nanoparticles exhibit efficient photothermal conversion, selectively damaging cancer cells. This approach offers heightened selectivity, as nanoparticles only aggregate in environments with cancer biomarkers present, sparing normal cells. Cytotoxicity assays confirm minimal toxicity to normal cells. In vivo studies on mice bearing solid tumors validate the system's efficacy in tumor regression. Overall, this study highlights the potential of nucleic acid-functionalized gold nanoparticles in intelligent and selective cancer photothermal therapy, offering insights for targeted diagnosis and treatment development. [ABSTRACT FROM AUTHOR]

ABSTRACT Background Aim Methods Results Conclusion Nevus of Ito and Mongolian spots are distinct clinical presentations of patchy dermal melanocytosis, characterized by similar dermatological manifestations that can pose diagnostic difficulties for clinicians.This review aims to consolidate current understanding and research advancements on these conditions to facilitate clinical diagnosis, differential diagnosis, and management.A comprehensive search of databases including PubMed and Google Scholar was conducted, along with an analysis of pertinent literature retrieved from reference lists spanning nearly four decades.Epidemiological, clinical, and pathological profiles exhibit nuanced differences between the two conditions, with unique expressions under electron microscopy and the regression possibility. It is noteworthy that most Mongolian spots naturally fade with advancing age, in contrast to nevus of Ito, which persist and may potentially evolve into malignant lesions. While picosecond laser treatment has shown greater efficacy than nanosecond lasers, the lower‐energy approach holds particular promise in pediatric cases. The therapeutic landscape for patchy dermal melanocytosis is evolving, shifting from selective photothermal action to photomechanical or subcellular photothermal modalities.This review underscores the importance of meticulous clinical assessment and the potential of innovative therapeutic approaches in managing these conditions. [ABSTRACT FROM AUTHOR]

Erastin, a ferroptosis-inducing system x c − inhibitor, faces clinical challenges due to suboptimal physicochemical and pharmacokinetic properties, as well as relatively low potency and off-target toxicity. Addressing these, we developed ECINs, a novel laser-responsive erastin-loaded nanomedicine utilizing indocyanine green (ICG)-grafted chondroitin sulfate A (CSA) derivatives. Our aim was to improve erastin's tumor targeting via CSA–CD44 interactions and enhance its antitumor efficacy through ICG's photothermal and photodynamic effects in the laser-on state while minimizing off-target effects in the laser-off state. ECINs, with their nanoscale size of 186.7 ± 1.1 nm and high erastin encapsulation efficiency of 93.0 ± 0.8%, showed excellent colloidal stability and sustained drug release up to 120 h. In vitro , ECINs demonstrated a mechanism of cancer cell inhibition via G1-phase cell cycle arrest, indicating a non-ferroptotic action. In vivo biodistribution studies in SK-HEP-1 xenograft mice revealed that ECINs significantly enhanced tumor distribution of erastin (1.9-fold greater than free erastin) while substantially reducing off-target accumulation in the lungs and spleen by 203-fold and 19.1-fold, respectively. Combined with laser irradiation, ECINs significantly decreased tumor size (2.6-fold, compared to free erastin; 2.4-fold, compared to ECINs without laser irradiation) with minimal systemic toxicity. This study highlights ECINs as a dual-modality approach for liver cancer treatment, demonstrating significant efficacy against tumors overexpressing CD44 and system x c −. Erastin-loaded chondroitin sulfate-propanesultone indocyanine green nanoparticles (ECINs) target CD44 and system x c − overexpressing hepatocellular carcinoma. Near-infrared laser irradiation at the tumor site triggers non-ferroptotic anticancer activity, further enhanced by phototherapy. [Display omitted] [ABSTRACT FROM AUTHOR]

Owing to the dense extracellular matrix and high interstitial fluid pressure in the tumor microenvironment, methods which enhance the permeation and retention of nano drugs into liver tumors remain unsatisfactory for successful tumor treatment. We designed a near-infrared (NIR)- and ultrasound (US)-triggered Pt/Pd-engineered "cluster bomb" (Pt/Pd-CB) which actively penetrates liver cancer cell membranes and achieves photothermal and sonodynamic therapy (SDT). The physical forces generated by the fast expansion and collapse of perfluoropentane nanodroplets eject "sub bombs" (Pt/Pd nanoalloys) into liver cancer cells upon activation by NIR and US. Pt/Pd nanoalloys can then convert H 2 O 2 into O 2 to alleviate hypoxia and boost SDT efficiency while exhibiting a highly efficient photothermal response under NIR irradiation. Our findings might especially be promising for the treatment of solid tumors. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] Rational design of the morphology and heterojunction to accelerate the separation of electron-hole pairs has played an indispensable role in improving the photocatalytic hydrogen evolution. ZnIn 2 S 4 (ZIS) has aroused considerable attention in solar-to-chemical energy conversion due to its remarkable photoelectrical properties and relatively negative energy band, whereas it still suffers from the severe photogenerated carrier recombination and catalyst aggregation. Herein, guided by density functional theory calculations, the constructed FeSe 2 @ZnIn 2 S 4 (FS@ZIS) heterojunction model has a hydrogen Gibbs free energy closer to zero compared with pure ZIS and FS, which is beneficial for hydrogen adsorption and desorption on the photocatalyst surface. Therefore, a novel cross-like core–shell FS@ZIS Step-scheme (S-scheme) heterojunction was synthesized successfully by in-situ growing ZIS nanosheets on the surface of cross-like FS. The structure with cross-like core–shell morphology not only inhibits the agglomeration of ZIS to increase specific surface area, but also provides a tight interface with S-scheme heterojunction. Moreover, the S-scheme heterojunction with a tight interface can effectively separate electron-hole pairs, leaving photoinduced charges with higher potentials. Furthermore, FS@ZIS-20 possesses exceptional photothermal capabilities, enabling the conversion of optical energy from visible and near infrared light to heat, thereby further enhancing the photocatalysis reaction. As a result, the cross-like core–shell FS@ZIS S-scheme heterojunction exhibits an excellent photocatalytic hydrogen evolution rate (7.640 mmol g−1 h−1), which is 24 times higher than that of pure ZIS (0.319 mmol g−1 h−1) under visible and near infrared light. Furthermore, employing more in-depth density functional theory calculations further investigates the charge transfer pathway of the FS@ZIS S-scheme heterojunction. This work provides insights into the construction of S-scheme heterojunctions with core–shell structure and photothermal effect for photocatalytic evolution hydrogen. [ABSTRACT FROM AUTHOR]

The active ingredient in traditional Chinese medicine, silybin (SBN), is known to inhibit the proliferation of cancer cells and synergistically enhance the anticancer effects of the chemotherapy drug doxorubicin (DOX). However, the combination of SBN and DOX faces challenges such as a lack of targeting, short half-lives, different administration routes, and pharmacokinetic processes, which prevent the drug combination from effectively targeting tumors and diminish their synergistic potential, thereby limiting their in vivo antitumor effects. In response, this study proposes the development of a novel nanocarrier system based on molybdenum disulfide (MoS₂) modified with polyethylene glycol (PEG) and sialic acid (SA) to co-deliver SBN and DOX. This system is designed to trigger the release of the drugs in response to dual stimuli of pH and near-infrared light, increasing the intracellular concentration of the drugs and enhancing their synergistic interaction. The MoS₂-LPN-SBN/DOX nanosystem circulates within the body and specifically accumulates at tumor sites due to the enhanced permeability and retention (EPR) effect and SA-mediated active targeting. Upon exposure to near-infrared light, the system provides combined chemo- and photothermal therapy, leading to significant tumor suppression. This research offers a new approach and strategy for the clinical treatment of lung cancer, suggesting a promising pathway for enhancing the efficacy of traditional therapies. [ABSTRACT FROM AUTHOR]

Utilization of the near‐infrared (NIR) light in the solar spectrum is critical for efficiency improvement of photocatalytic H2 evolution. However, common semiconductors have low response to the NIR light and narrow bandgap semiconductors have inappropriate redox potentials. Here, the study presents a new dual‐functional up‐conversion strategy in one sensitizer for promoting photocatalytic hydrogen production reactions by converting NIR light to visible light and high‐energy electrons simultaneously, via photon‐photon conversion and photo‐electronic process, respectively. Using WO3:Yb,Er as the sensitizer and Zn0.5Cd0.5S as the hydrogen evolution reaction catalyst, a photocatalytic hydrogen release rate of 24.3 mmol g−1 h−1 under simulated solar‐light has been achieved without using any co‐catalyst. After loading Ni2P as a co‐catalyst, the photocatalytic hydrogen production performance can be further improved to 41.3 mmol g−1 h−1 at 10 °C and 93.3 mmol g−1 h−1 under non‐temperature‐controlled conditions, exceeding most photocatalysts. This work offers a new strategy to improve the NIR light utilization of the solar‐light for promoting photocatalytic hydrogen generation through synergistic photo‐optical, photo‐electronic, and photo‐thermal effects. [ABSTRACT FROM AUTHOR]

Some creatures have periodic nanostructures and chromophores in their flexible organs that allow them to control the color and shape of their skin. Artificial photonic structures that can mimic the aforementioned ability of these natural structures are researched extensively. In this study, polydopamine‐incorporated core–interlayer–shell (CIS‐PDA) nanoparticles capable of shape reconfiguration and expressing vivid structural colors are designed. These nanoparticles can be readily assembled to produce colloidal photonic crystals (CPhCs) and can exhibit vivid structural colors by virtue of their light‐absorbing capability. Soft CPhC films prepared with these nanoparticles undergo stable elastic deformation at 15% strain and exhibit mechanochromic properties. Specifically, the PDA in the CIS nanoparticles can absorb broadband light and exhibit a photothermal effect resembling that of melanosomes in living organisms, which enables self‐healing between multiple CPhC films. Due to their favorable properties, the CPhC films prepared in this study represent promising photothermally reconfigurable photonic materials. Moreover, arbitrarily shaped 2D or 3D surfaces are conformally coated with the films via microimprinting or vacuum wrapping, courtesy of the reconfigurability of these films. These findings suggest that CPhC films prepared with CIS‐PDA nanoparticles can be used as form‐free mechanochromic strain sensors and nonfading optical films for industrial products. [ABSTRACT FROM AUTHOR]

Glioblastoma (GBM) is one of the deadliest primary brain tumors, but its diagnosis and curative therapy still remain a big challenge. Herein, neutrophil‐targeting semiconducting polymer nanotheranostics (SSPNiNO) is reported for second near‐infrared (NIR‐II) fluorescence imaging‐guided trimodal therapy of orthotopic glioblastoma in mouse models. The SSPNiNO are formed based on two semiconducting polymers acting as NIR‐II fluorescence probe as well as photothermal conversion agent, respectively. A thermal‐responsive nitric oxide (NO) donor and an adenosine 2A receptor (A2AR) inhibitor are co‐integrated into SSPNiNO to enable trimodal therapeutic actions. SSPNiNO are surface attached with a neutrophil‐targeting ligand to mediate their effective delivery into orthotopic GBM sites via a "Trojan Horse" manner, enabling high‐sensitive NIR‐II fluorescence imaging. Upon NIR‐II light illumination, SSPNiNO effectively generates heat via NIR‐II photothermal effect, which not only kills tumor cells and induces immunogenic cell death (ICD), but also triggers controlled NO release to strengthen tumor ICD. Additionally, the encapsulated A2AR inhibitor can modulate immunosuppressive tumor microenvironment by blocking adenosine‐A2AR pathway, which further boosts the antitumor immunological effect to observably suppress the orthotopic GBM progression. This study can provide a multifunctional theranostic nanoplatform with cumulative therapeutic actions for NIR‐II fluorescence imaging‐guided effective GBM treatment. [ABSTRACT FROM AUTHOR]

Marine biofouling, which is one of the technical challenges hindering the growth of the marine economy, has been controlled using cuprous oxide (Cu2O) nanoparticles due to the exceptional antifouling properties of Cu(I) ions. However, Cu2O nanoparticles have encountered bottlenecks due to explosive releases of Cu+ ions, high toxicity at elevated doses, and long‐term instability. Here, we present a novel method called Redox Concomitant Formation (RCF) for fabricating a hierarchical Cu(I) metal–organic framework polypyrrole (Cu(I)−MOF/PPy) composite. This method enables in situ phase transition via successive redox reactions that change the chemical valence state and coordination mode of Cu(II)−MOF, resulting in a new structure of Cu(I)−MOF while creating a PPy layer surrounded by the hierarchical structure. Owing to the steady release of Cu+ ions from the Cu(I) sites and photothermal properties of PPy, Cu(I)−MOF/PPy exhibits superior and broad‐spectrum resistance to marine bacteria, algae, and surface‐adhered biofilms in complex biological environments, as well as long‐term stability, resulting in 100 % eradication efficiency under solar‐driven heating. Mechanistic insights into successive structural redox reactions and formation using the RCF method are provided in detail, enabling the fabrication of novel MOFs with the desired composition and structure for a wide range of potential applications. [ABSTRACT FROM AUTHOR]

The capacity to withstand challenges posed by complex environments is crucial for developing advanced high‐performance protective materials with mechanically adjustable nature. By constructing long‐range hierarchical network of shear‐stiffening gel‐carbon nanotube‐cellulose nanofiber (SCC) embedded within epoxy resin (ER), this work engineers a nacre‐inspired variable‐stiffness SCC‐ER composite (SCCE). Lightweight SCC scaffold attenuates falling impact force from 2.23 to 0.46 kN, and reaches 60 °C within 20 s under 1 sun exposure. Additionally, owing to the rigid ER matrix, SCCE exhibits 4.03 GPa elastic modulus, outperforming numerous conventional engineering materials in puncture resistance. Specific energy absorption of nacre‐mimetic SCCE presents 1.91 MJ m−3 while that of random structural SCCE is only 0.50 MJ m−3. More importantly, SCCE features representative photothermal‐induced reversible rigidity whose storage modulus varies from 9.85 MPa at 30 °C to 11.61 kPa at 116 °C under light stimulation. It also presents shape‐programmability, capable of adhering complex structural surfaces for protection. Eventually, SCCE‐based semi‐active adjustable protectors are constructed that leverage contactless photothermal effect to modulate rigidity. 5 mm‐thick smart SCCE‐protectors resist 163.93 m s−1 ballistic impact while 15‐mm commercial kneepads are penetrated at lower speed of 136.98 m s−1. This bio‐inspired semi‐active strategy proposes a promising avenue for enhancing personal protective equipment. [ABSTRACT FROM AUTHOR]

Solar energy can be harnessed and converted into heat via the photothermal effect, which can then be utilized to drive many other reactions to produce important resources, such as water, fuel, electricity, and even mechanical actuation in a clean and sustainable manner. Hydrogels and membranes coupled with photothermal materials are particularly suitable for this purpose because they possess advantageous properties, such as porosity and adaptability. These properties allow for the introduction of diverse additives and functionalities, ensuring that photothermal systems can be customized for specific tasks, thereby enhancing their overall performance, functionality and versatility. This review aims to provide an overview of recent developments and the significance of employing photothermal hydrogels and membranes in multiple fields ranging from clean water, fuel production, electricity generation to mechanical actuation, followed by a discussion on key considerations in materials design and engineering. Finally, the review addresses the challenges and future directions of photothermal applications. [ABSTRACT FROM AUTHOR]

Polyvinyl chloride (PVC), a synthetic plastic notable for harmful emissions during deterioration, has potential to be molecularly adjusted by photo‐oxidative ultraviolet degradation. This research investigates the influence of electron beam irradiation and near‐infrared photothermal treatment utilizing gold nanoparticles to establish the optimized molecular weight and beam time exposure for biodegradable PVC properties while maintaining a minimum tensile strength as measured through the ratio of peak tension force by cross sectional area. PVC powder samples with number‐average molecular weights ranging from 20.0 to 90.0 kDa and varying exposure times of a 100 kGy electron beam from 80 to 115 ms are employed for the study. Outcomes from PVC irradiation reveal the optimal parameters for inducing biodegradability in samples: an e‐beam exposure duration of 95 ms applied to PVC powder with a sample molecular weight of 20.0 kDa. Analysis of the ratio of number average molecular weight Mn$ {{M}_{\mathrm{n}}} $ and weight average molecular weight Mw$ {{M}_{\mathrm{w}}} $ demonstrates that shorter irradiation durations result in lower molecular weights and molecular weight is directly proportional to Tg and crystallinity. Future work aims to scale up the procedure to industrial applications and investigate the treatment's applicability to a variety of thermoplastics. [ABSTRACT FROM AUTHOR]

As catalytic research has advanced, with many teams striving to enhance efficiency by developing efficient catalysts and utilizing photothermal synergy to strengthen reaction mechanisms. Photothermal-assisted photocatalysis combines photothermal effects with photocatalysis, exhibiting superior photo-absorption properties and boosted photocatalytic activity compared to individual photocatalysis, which concurrently enhances solar energy utilization. This review delineates the application of graphitic carbon nitride (g-C 3 N 4)-based photocatalysts with photothermal-assisted photocatalysis across various realms, including water splitting for H 2 production, CO 2 reduction, pollutant degradation and sterilization. This integration not only overcomes the limitations of individual photocatalysis and thermocatalysis but also enhances catalytic activity significantly, leading to substantial improvements in product yields for specific reactions. Conclusively, this review provides a detailed analysis of the benefits and challenges of g–C 3 N 4 –based photothermal assisted photocatalysis, forecasts its future development, and proposes research directions to advance g–C 3 N 4 –based systems for energy and environmental applications, thus contributing to sustainable ecological progress and addressing energy challenges. • An in-depth mechanism analysis of photothermal-assisted photocatalysis was studied. • Advancements of g–C 3 N 4 –based photothermal-assisted photocatalysis was examined. • Perspectives on the future development of photothermal-assisted photocatalysis was provided. [ABSTRACT FROM AUTHOR]

Amphiphilic peptides have garnered significant attention due to their highly designable and self‐assembling behaviors. Self‐assembled peptides hold excellent potential in various fields such as biosensing, environmental monitoring, and drug delivery, owing to their remarkable biological, physical, and chemical properties. While nanomaterials formed by peptide self‐assembly have found widespread use in biomedical applications, the development of 2D peptide nanosheets based on the self‐assembly of amphiphilic peptides remains challenging in terms of rational design and morphology modulation. In this study, rationally designed amphiphilic peptide molecules are self‐assembled into peptide nanosheets (PNS) under specific conditions to encapsulate gold nanoparticles (AuNPs), resulting in the formation of AuNPs/PNS hybrid materials with high photothermal conversion efficiency. The findings demonstrate that 2D PNS enhances the overall photothermal therapy effect of the nanohybrid materials due to their larger hosting area for AuNPs and higher biocompatibility. The well‐designed amphiphilic peptides in this study offer insights into the structural design and functional modulation of self‐assembled molecules. In addition, the constructed biomimetic‐functional 2D inorganic/organic nanohybrid materials hold potential applications in biomedical engineering. [ABSTRACT FROM AUTHOR]

Photothermal therapy (PTT) is a promising non-invasive treatment that has shown great potential in eliminating tumors. It not only induces apoptosis of cancer cells but also triggers immunogenic cell death (ICD) which could activate the immune system against cancer. However, the immunosuppressive tumor microenvironment (TIME) poses a challenge to triggering strong immune responses with a single treatment, thus limiting the therapeutic effect of cancer immunotherapy. In this study, dual-targeted nano delivery system (GOx@FeNPs) combined with αPD-L1 immune checkpoint blocker could inhibit colorectal cancer (CRC) progression by mediating PTT, ferroptosis and anti-tumor immune response. Briefly, specific tumor delivery was achieved by the cyclic arginine glycyl aspartate (cRGD) peptide and anisamide (AA) in GOx@FeNPs which not only had a good photothermal effect to realize PTT and induce ICD, but also could deplete glutathione (GSH) and catalyze the production of reactive oxygen species (ROS) from endogenous H2O2. All these accelerated the Fenton reaction and augmented the process of PTT-induced ICD. Thus, a large amount of tumor specific antigen was released to stimulate the maturation of dendritic cells (DCs) in lymph nodes and enhance the infiltration of CD8+ T cells in tumor. At the same time, the combination with αPD-L1 has favorable synergistic effectiveness against CRC with tumor inhibition rate over 90%. Furthermore, GOx@FeNPs had good magnetic resonance imaging (MRI) capability under T2-weighting owing to the presence of Fe3+, which is favorable for integrated diagnosis and treatment systems of CRC. By constructing a dual-targeted GOx@FeNPs nanoplatform, PTT synergistically combined with ferroptosis was realized to improve the immunotherapeutic effect, providing a new approach for CRC immunotherapy. [ABSTRACT FROM AUTHOR]

Open nanoshells such as nanobowls or nanocups collectively described as 'semi shells' have unique plasmonic properties due to their lack of symmetry. So far, their fabrication was based on multistep and laborious methods such as solid state sputter coating or selective deposition/etching using sacrificial templates. In this work, we report a rapid one step colloidal synthetic protocol for PEGylated semi-shell (SS) fabrication by simultaneous facet specific anisotropic chemical etching of rhombic dodecahedral ZIF-8 and heterogenous nucleation & growth of gold. The SS possesses a strong localized surface plasmon resonance in the near-infrared region, which is retained after surface passivation with polyethylene glycol and subsequent cryopreservation for extended shelf-life. Freshly reconstituted PEGylated SS was found to be safe & non-toxic in healthy C57BL/6 mice post intravenous administration. The PEGylated SS displayed significant photothermal efficiency of ~37% with 808 nm laser irradiation. Preclinical assessment of intra-tumoral photothermal efficacy indicated complete remission of primary breast tumor mass with insignificant metastasis to vital organs in 4T1 FL2 tumor bearing CD1 nude mice. Further, PEGylated SS mediated photothermal therapy also yielded morbidity free survivael of 75% for up to 90 days, indicating their potential to significantly improve outcomes in advanced breast tumors. Anisotropic gold-based colloidal nanoparticles such as semi shells have unique optical properties and widespread applications such as in bioimaging, biosensing and therapy, however, the fabrication process of semi shells remains a challenge due to laborious multistep solid state and colloidal procedures. In this study, the authors develop a rapid one-pot colloidal synthetic route for the fabrication of semi shells using ZIF-8 as a sacrificial template, and demonstrate their promise for photothermal therapy. [ABSTRACT FROM AUTHOR]

The emergence of global warming issues has triggered the interest in producing carbon-neutral energy sources and fossil-based chemicals from affordable and renewable feedstocks (e.g., bio-ethanol). Herein, the synthesis of highly dispersed CuS/TiO 2 photothermal catalysts is reported for simultaneously converting ethanol into hydrogen and acetaldehyde under simulated sunlight. The catalyst achieved a hydrogen evolution rate of 51.61 mmol g−1 h−1 and an acetaldehyde production rate of 48.63 mmol g−1 h−1, with a maximal acetaldehyde selectivity of 97% among carbon-containing products. Compared to pristine TiO 2 , the introduction of plasmonic CuS largely extended the light adsorption range and enhanced the photothermal performance, whilst the formation of heterojunction structure improved the charge transfer and separation efficiency. The density functional theory calculation results demonstrate that CuS/TiO 2 composite interfaces could significantly lower the activation energy of ethanol dehydrogenation reaction and improve hydrogen evolution reaction ability. This study provides deep insight into understanding and optimizing hot carrier dynamics in photothermal catalytic systems. • Novel CuS/TiO 2 catalyst for efficient ethanol dehydrogenation to co-produce hydrogen and acetaldehyde under mild conditions. • 0.05 CuS/TiO 2 achieved a H 2 evolution rate of 51.61 mmol g−1 h−1 and an acetaldehyde production rate of 48.63 mmol g−1 h−1. • Synergistic effects of heterojunction and significant photothermal effect induced by CuS enhanced catalytic performance. • Reduced activation energy for ethanol dehydrogenation and improved H 2 evolution were achieved by CuS/TiO2 interface. [ABSTRACT FROM AUTHOR]

This novel study unfolds the heat and mass transfer investigation of Williamson nanofluid (WNF) through a porous medium past a stretching plate, along with considering heat generation/absorption. Nanoparticles hold significant significance in thermal engineering, industrial operations, and biomedical advancements, contributing to enhanced heat transfer, cooling mechanisms, thermal extrusion processes, and applications in cancer treatment, particularly in addressing brain tumors. The coupled ordinary differential equations (ODEs) are gained from governing partial differential equations (PDEs) by applying sufficient transformations. Then the ODEs of a nonlinear nature, along with boundary conditions, are solved through bvp4c, a built-in MATLAB program. A good agreement has been found in comparing the present study with already published papers. Numerical values for skin friction, mass transfer, and heat transfer are shown through a table against involved physical parameters, especially for both injection (S < 0) and suction (S > 0) cases, by varying the values of unsteadiness parameter A and Weissenberg number W e . The effects of the physical parameters on velocity, temperature, and mass profile are graphically depicted and illustrated minutely. It is noted that both the magnetic and Williamson parameters cause the thickness of the boundary layer to be reduced. It can be deduced from these findings that the rate of heat transfer over the surface of the plate decreases as the unsteadiness parameter increases. Furthermore, it is observed that an increase in the parameters of thermophoresis and Brownian motion leads to a higher temperature of the nanofluid. [ABSTRACT FROM AUTHOR]

Recent advances are achieved in the design and development of efficient organic photosensitizers (PSs), especially with fluorescence imaging navigation in the second near‐infrared (NIR‐II, 1000–1700 nm) region. However, there are simply a handful of NIR‐II emissive organic PSs with efficient oxygen‐independent capability due to the scarcity of high‐performance NIR‐responsive organic materials and targeted delivery. Herein, a NIR‐II‐emissive organic nanomedicine with biomimetic engineering for high‐performance NIR‐II imaging and targeted multiple phototherapies of pancreatic tumors is reported. An A‐D‐A‐type conjugated small‐molecule TPC is designed and used to prepare water‐dispersive nanoparticles, which demonstrated high efficiency for type I and type II photodynamic performances, good photothermal conversion of 57%, and bright NIR‐II emission with a quantum yield of 9.8% under 808 nm light irradiation. With pancreatic cancer cell membrane camouflage, the biomimetic TPC nanomedicine achieved high‐resolution and targeted bioimaging of whole‐body blood vessels and tumors. Antitumor experiments demonstrated the high efficiency of the biomimetic TPC nanomedicine for pancreatic tumor elimination and good biosafety with 808 nm light irradiation. This work demonstrated a NIR‐II‐emissive versatile nanomedicine with enhanced tumor‐targeting for high‐resolution NIR‐II bioimaging and superior phototheranostics, providing a feasible idea for the evolution of targeted and high‐performance theranostics. [ABSTRACT FROM AUTHOR]

Efficient removal of uranium from uranium‐containing nuclear wastewater is of great significance for utilizing uranium resources and protecting the environment from uranium hazards. In this paper, a polyamidoxime‐coated coconut haustorium derived magnetic biochar (CHMBC‐PAO) composite adsorbent with excellent adsorption performance, magnetism, recyclability, and photothermal conversion properties in complex environments is prepared through a simple soak‐gelation coating method for efficient removal of uranium from nuclear wastewater. The coconut haustorium biochar, carbonized by a sponge‐like organ inside the sprouted coconut, can provide rich functional groups and electronegative surface, which are conducive to the loading of functional materials and the adsorption of uranyl, respectively. The CHMBC‐PAO presents 2.4 emu g−1 saturation magnetization, making it can be efficiently recovered through magnetic recovery. It can convert absorbed light into thermal energy through molecular thermal vibration and non‐radiative relaxation process of excitons. Enhanced by the photothermal effect, CHMBC‐PAO shows an extra high uranium adsorption capacity of 310.30 mg g−1 in acidic nuclear wastewater within a short period of time, surpassing the adsorption capacity of most reported uranium removal materials. Meanwhile, the CHMBC‐PAO also presented excellent ion selectivity and reusability. Therefore, CHMBC‐PAO composite adsorbent can be considered as a potential candidate for treating radioactive nuclear wastewater. [ABSTRACT FROM AUTHOR]

Bone defects arising from trauma and tumors present a potential risk of infection and compromise host immune function. Within a dysfunctional microenvironment, the uncontrolled breeding of bacteria and persistent chronic inflammation exacerbate bone loss, impeding bone regeneration and repair. Macrophages function as specialized phagocytes within the immune microenvironment and the orchestrated role of distinct phenotypes during regeneration has attracted significant attention. The M1 phenotype exhibits antimicrobial activities to eliminate bacterial threats, while the M2 phenotype secretes anti‐inflammatory mediators to fine‐tune the immune microenvironment. Here, a biphasic delivery system consisting of a photothermal agent (graphene oxide, GO) coated and an immune modulator (urolithin A, UA) encapsulated in coaxial electrospun nanofibers with a dynamic regulation function of macrophage behavior is designed. It is observed that the GO coating exhibited remarkable photothermal performance within the near‐infrared window, affecting the phagocytic activity of macrophage subsets in an integrin‐RhoA‐ROCK1 dependent manner. The sustained release of UA from the core layer induced a phenotypic switch by downregulating TNF signaling and upregulating TGF signaling. This system also demonstrated a promotion of bone regeneration in vivo. Overall, this strategy achieved sequential regulation of macrophage phenotypes, effectively preventing infection and fostering bone tissue regeneration. [ABSTRACT FROM AUTHOR]

Hygroscopic salt hydrogel photothermal composites and related technology are a promising pathway for water harvesting. However, due to the overly cumbersome preparation process, the distribution of the surface photothermal layer is difficult to control and the photothermal efficiency is low. In this paper, a method is proposed to greatly simplify the preparation process of photothermal layer hydrogels and improve their atmospheric water harvesting performance by constructing temperature‐sensitive interpenetrating networks. Due to the decomposition of some reversible hydrated structures in the network during heating and warming, carbon nanotubes move autonomously to form a layered structure with a photothermal effect on the upper surface, which can return to its original state after cooling and remain stable at room temperature or under solar illumination. Compared with hydrogels with general layered structure or overall distribution of photothermal materials, agar/GG/PAM/CNT hydrogel has faster moisture adsorption efficiency and higher desorption efficiency, and during the 24 h continuous sorption–desorption cycle is capable of achieving high water yield of 2.57 Lwater kgsorbents−1 day−1, superior to most recent hydrogel adsorbents. Simplifying the preparation process while maintaining high efficiency, while greatly improving photothermal performance, paves the way for cost‐effective mass production applications for a wide range of hygroscopic salt‐hydrogel photothermal composites. [ABSTRACT FROM AUTHOR]

Hydrogel dressings play an important role in the treatment of bacterial infection. In this study, carboxymethyl chitosan (CM‐CS) was cross‐linked with aldehyde polyglycol (DF‐PEG), and then polydopamine (pDA) and 5,10,15, 20‐tetrakis (4‐aminophenyl) porphyrin (TAPP) were grafted to prepare a CM‐CS/DF‐PEG/pDA/TAPP hydrogel (CDPT). The results showed that the CDPT hydrogel had good adhesion, injectability, self‐healing, degradability, and biocompatibility. Under near‐infrared irradiation, the CDPT hydrogel has excellent photothermal and photodynamic effects and can effectively inhibit activity of Staphylococcus aureus (S. aureus), Escherichia coli (E. coli) and antibiotic‐resistant, methicillin‐resistant Staphylococcus aureus (MRSA). In summary, CDPT hydrogel has potential applications as antibacterial material. [ABSTRACT FROM AUTHOR]

Over the past few decades, polymers with dynamic covalent bonds have received a lot of attention due to their self‐healing, shape memory, and environmental adaptation properties. However, most of them require a change in catalyst or environmental conditions to achieve bond reduction and exchange reactions, and the harsh conditions are not conducive to the practical application of the material. However, the dr‐polyurea based polyurethane (PUU) can be prepared at low temperatures, and can be worn and rebuilt in a catalyst free and mild environment, thus showing excellent self‐healing function. In this paper, the unique dynamic reaction mechanism of hindered urea bond (HUB), the properties of related polymers and the development of frontier are reviewed. In addition, the performance research of HUB and the application prospect of innovative synthetic PUU are also reviewed. [ABSTRACT FROM AUTHOR]

The development of photocatalysts that maximize the utilization of the solar spectrum is crucial to achieving efficient photocatalysis. Herein, the synthesized W 18 O 49 @ZnIn 2 S 4 hollow hierarchical structure exhibits superior photothermal-assisted hydrogen (H 2) photocatalytic performance under full solar spectrum irradiation. Within this photocatalyst design framework, the use of hollow spherical W 18 O 49 exploits the Localized Surface Plasmon Resonance (LSPR) effect, resulting in increased light absorption. This imparts additional energy to photogenerate carriers through ZnIn 2 S 4 , expediting charge migration and elevating the temperature of the reaction system, consequently facilitating the separation of carriers. Notably, the optimized WO(16h)@ZIS-10 sample shows impressive hydrogen evolution rates of 3.11 mmol g−1 under sunlight exposure and 4.98 mmol g−1 h−1 under composite illumination of AM 1.5G and near-infrared (NIR). Additionally, the study explores the impact of different heating methods on photocatalytic activity in solid-liquid reactions, providing valuable insights into effective solar energy conversion through high-activity solar-assisted photocatalysts. The W 18 O 49 @ZnIn 2 S 4 photothermal catalysts with suitable core-shell thickness was developed, which can efficiently utilize the hot electrons from LSPR effect, thus display a superior hydrogen evolution performance with photothermal synergistic effect. [Display omitted] • Successful construction of a hollow layered structure of core-shell W 18 O 49 @ZnIn 2 S 4. • High hydrogen production activity and stability. • Good practical application prospect. [ABSTRACT FROM AUTHOR]

The crucial point of solar thermal utilization makes solar heat collector gathering much attention. In this study, imitating polar bears' fur structure, fluorescent materials are modified into a solar heat collector, and the photothermal conversion is evaluated to examine the influence of polyvinyl alcohol concentration, fluorescent luminescence type and fluorescence concentration. The test results indicate that fluorescent materials that has a greater Stokes shift show the greater photothermal effect. Moreover, when composed of a PVA concentration being 5.0% and a fluorescent concentration being 0.50%, the composites exhibit the maximal photothermal conversion temperature (99.4°C) that is 17.9% higher than that of the solar heat collectors without fluorescent materials. This study proposes creating solar heat collector with modified fluorescent materials, and the new perspective of which demonstrates that the composites have a great potential and application prospect in the solar photothermal field. [ABSTRACT FROM AUTHOR]

Metal nanocages exhibit localized surface plasmon resonance that strongly absorbs and scatters light at specific wavelengths, making them potentially valuable for photothermal therapy and biological imaging applications. However, investigations on metal nanocages are still confined to high-cost and small-scale synthesis. The comprehensive analysis of optical properties and optimal size parameters of metal nanocages is rarely reported. This paper simulates the effects of materials (Ag, Au, and Cu), size parameters, refractive index of the surrounding medium, and orientation on the light absorption and scattering characteristics of the nanocages using the finite-element method and the size-dependent refractive-index model for metal nanoparticles. The results show that the Ag nanocages have excellent light absorption and scattering characteristics and respond significantly to the size parameters, while the refractive index and orientation of the surrounding medium have less effect on them. The Au nanocages also possess superior light absorption properties at specific incident wavelengths. This study also identified the optimized sizes of three metal nanocages at incident light wavelengths commonly used in biomedicine; it was also found that, under deep therapy conditions, Ag nanocages in particular exhibit the highest volume absorption and scattering coefficients of 0.708 nm−1 and 0.583 nm−1, respectively. These findings offer theoretical insights into preparing target nanocage particles for applications in photothermal therapy and biological imaging. [ABSTRACT FROM AUTHOR]

Thermal lens spectrometry is a high-sensitivity method for measuring the optical and thermal parameters of samples of different nature. To obtain both thermal diffusivity and absorbance-based signal measurements with high accuracy and precision, it is necessary to pay attention to the factors that influence the trueness of photothermal measurements. In this study, the features of liquid objects are studied, and the influence of optical and thermal effects accompanying photothermal phenomena are investigated. Thermal lens analysis of dispersed solutions and systems with photoinduced activity is associated with a large number of side effects, the impact of which on trueness is not always possible to determine. It is necessary to take into account the physicochemical properties and optical and morphological features of the nanophase and components exhibiting photoinduced activity. The results obtained make it possible to reduce systematic and random errors in determining the thermal-diffusivity-based and absorbance-based photothermal signals for liquid objects, and also contribute to a deeper understanding of the physicochemical processes in the sample. [ABSTRACT FROM AUTHOR]

Cancer therapy is constantly evolving, with a growing emphasis on targeted and efficient treatment options. In this context, graphene quantum dots (GQDs) have emerged as promising agents for precise drug and gene delivery due to their unique attributes, such as high surface area, photoluminescence, up-conversion photoluminescence, and biocompatibility. GQDs can damage cancer cells and exhibit intrinsic photothermal conversion and singlet oxygen generation efficiency under specific light irradiation, enhancing their effectiveness. They serve as direct therapeutic agents and versatile drug delivery platforms capable of being easily functionalized with various targeting molecules and therapeutic agents. However, challenges such as achieving uniform size and morphology, precise bandgap engineering, and scalability, along with minimizing cytotoxicity and the environmental impact of their production, must be addressed. Additionally, there is a need for a more comprehensive understanding of cellular mechanisms and drug release processes, as well as improved purification methods. Integrating GQDs into existing drug delivery systems enhances the efficacy of traditional treatments, offering more efficient and less invasive options for cancer patients. This review highlights the transformative potential of GQDs in cancer therapy while acknowledging the challenges that researchers must overcome for broader application. [ABSTRACT FROM AUTHOR]

The development of absorber materials with strong light absorption properties and low-cost fabrication processes is highly significant for the application of photothermal conversion technology. In this work, a mixed powder consisting of NaCl, polypropylene (PP), and scale-like carbon flakes was ultrasonically pressed into sheets, and the NaCl was then removed by salt dissolution to obtain porous carbon polypropylene composite sheets (P-CPCS). This process is simple, green, and suitable for the low-cost, large-area fabrication of P-CPCS. P-CPCS has a well-distributed porous structure containing internal and external connected water paths. Under the dual effects of the carbon flakes and porous structure, P-CPCS shows excellent photothermal conversion performance in a broad wavelength range. P-CPCS-40 achieves a high temperature of 128 °C and a rapid heating rate of 12.4 °C/s under laser irradiation (808 nm wavelength, 1.2 W/cm2 power). When utilized for solar steam generation under 1 sun irradiation, P-CPCS-40 achieves 98.2% evaporation efficiency and a 1.81 kg m−2 h−1 evaporation rate. This performance means that P-CPCS-40 outperforms most other previously reported absorbers in terms of evaporation efficiency. The combination of carbon flakes, which provide a photothermal effect, and a porous polymer structure, which provides light-capturing properties, opens up a new strategy for desalination, sewage treatment, and other related fields. [ABSTRACT FROM AUTHOR]

This study presents a novel multimodal cancer theranostic platform developed using tumor cell‐coated biomimetic carbon nanohorn (CNH) complexes that encapsulate the anticancer drug paclitaxel (PTX). This platform combines photothermal therapy, chemotherapy, and immunotherapy to fight against malignant colorectal cancer. These engineered nanocomplexes are designed to deliver sufficient PTX molecules into a targeted solid tumor in a light‐controllable manner while inducing significant photothermal and antitumor immune responses. The outstanding photothermal conversion property of the CNHs under near‐infrared light enables effective cancer cell ablation and awakening of cytotoxic immune responses. Tumor cell membrane‐coated CNHs show improved water dispersibility, immune evasion, and targeting capabilities alongside enhanced immune activation against tumors. The efficacy of the biomimetic functional CNH nanocomplexes is demonstrated through excellent tumor‐targeting, controlled drug‐releasing behavior, and induction of cancer cell death, contributing to a robust antitumor response. This study provides a promising approach to cancer treatment by integrating multiple therapeutic modalities into a single platform, potentially enhancing treatment efficacy to combat intractable cancer. [ABSTRACT FROM AUTHOR]

Cisplatin (CDDP) is an FDA‐approved chemotherapeutic drug used for treating various solid tumors. Despite of its effectiveness towards chemotherapy, it faces several challenges, such as multi‐drug resistance (MDR) and significant damage to the normal tissues. To address these challenges, various nanoformulations were developed to improve the delivery and safety of CDDP. One of the limitation in these CDDP loaded nanoformulations is that the effective CDDP loading concentrations are very poor. Therefore, this leaves a grand challenge to develop an effective strategy to carry higher concentrations of CDDP molecules, and also simultaneously exhibit very unique properties. Herein, we have developed an one‐pot synthesis of Cisplatin encapsulated Plasmonic blackbody (CiP), which offers a double play for near infrared (NIR) light activatable chemo‐photothermal therapy in destructing cancer cells as well as mediate catalytic reduction of 4‐nitrophenol (4‐NP). The CiP nanoformulation exhibits superior light absorbing capabilities in the NIR region with an appreciable photothermal conversion efficiency of 41 %. Further, NIR light activatable combinatorial therapeutic approach of CiP was demonstrated against ovarian cancer cells and as a catalyst for the reduction of model pollutant 4‐nitrophenol. Our findings highlight the potential of CiP as a versatile platform for light‐activated combinatorial cancer therapy and environmental pollutant remediation. [ABSTRACT FROM AUTHOR]

Developing photocatalysts with desired activity and stability toward hydrogen evolution reaction (HER) in alkaline seawater is of prime significance but still pressingly challenging. Herein, cuprum nanoclusters (CuNCs) are anchored on the surface of cadmium sulphide homojunctions (CdS‐H) with unsaturated edge sulphur (S) by an in situ photoreduction technique, which promotes the stability and hydrogen evolution of photocatalyst in the process of alkaline seawater hydrogen (H2) evolution (15.5 mmol g−1 h−1) with an apparent quantum yield of 11.0% at 450.0 nm. It is comprehensively confirmed that the unsaturated edge S not only effectively anchored Cu NCs but also promoted the adsorption of chloride ion (Cl−) ions, which suppressed the oxidation of lattice S and modulated the stability of the photocatalyst in alkaline seawater. The photothermal effect induced by the anchored Cu NCs accelerated the reaction kinetics, and the directional migration of the photocarrier at the metal‐semiconductor interface is demonstrated via the in situ method. This work affords a new perspective to rational design photocatalysts with high stability and superior performance in alkaline seawater. [ABSTRACT FROM AUTHOR]

Near‐infrared (NIR) photodetection and imaging have sparked significant interests across a wide range of applications. While silicon photodiodes are commonly employed, the small light absorption coefficients of Si in NIR severely limit the performance, especially in the case of thin active Si layers. Although various light harvesting techniques are proposed to increase light absorption of Si, pixel‐level strategy for enhanced NIR imaging is still challenging in CMOS image sensors (CISs) with a pixel size in only a micron scale. In this paper, plasmonic metasurfaces are intimately integrated on top of 2.3 µm thick Si active regions of the pixels of a backside illumination (BI)‐CIS for NIR imaging for the first time. 200% improved photoresponsivity is obtained in experiments in such a planar Si layer rather than patterning the Si layer with potential damage to the active region. Numerical simulation results reveal highly enhanced light intensity in the thin active Si layer due to the presence of plasmonic metasurfaces. Significantly improved imaging brightness and signal‐to‐noise ratio of NIR imaging are demonstrated under both laser and LED illumination. This CMOS‐compatible technique is expected to hold promising potentials in applications including machine vision, iris certification, light detection and ranging (LiDAR), and optical communication in data centers. [ABSTRACT FROM AUTHOR]

The precise and safe treatment of bioorthogonal prodrug system is hindered by separate administration of prodrug and its activator, which often results in poor therapeutic effects and severe side effects. To address above issues, we herein construct a single bioorthogonal-activated co-delivery system for simultaneous PROTAC prodrug (proPROTAC) delivery and controlled, site-specific activation for tumor-specific treatment. In this co-delivery system (termed AuPLs), prodrug (proPROTAC) and water-soluble Pd-catalyst are first encapsulated by gold nanocubes (AuNCs), which are further coated with a layer of phase-change material (lauric acid/stearic acid, LA/SA). Below 39 °C, the solid state of LA/SA prevents the activation of Pd-mediated bioorthogonal reaction due to the solidification of Pd-catalyst and proPROTAC. Nevertheless, once over 42 °C, the phase change of LA/SA into liquid state, enabled by the photothermal effect of AuNCs, triggers the simultaneous release of proPROTAC and Pd-catalyst and initiates the in situ bioorthogonal reaction for proPROTAC activation. In the tumor-bearing mouse models, the systemic administration of AuPLs results in the accumulation in tumor region, where the photothermal effect activates and controls the tumor-specific bioorthogonal reaction to degrade BRD4 protein, leading to anti-tumor effects with minimized side effects. Overall, the co-delivery proPROTAC and Pd-catalyst and controlled activation by photothermal effects provide a precise way for biorthogonal-based anticancer prodrugs. [Display omitted] [ABSTRACT FROM AUTHOR]

Corneal neovascularization (CNV) is a major cause of blindness worldwide. However, the recent drug treatment is limited by repeated administration and low drug bioavailability. In this work, SU6668 (an inhibitor of receptor tyrosine kinases) and indocyanine green (ICG) are loaded onto poly(lactic- co -glycolic acid) (PLGA) nanoparticles, and then coated with anti-VEGFR2 single chain antibody (AbVr2 scFv) genetically engineered cell membrane vesicles. The nanomedicine is delivered via eye drops, and the hyperthermia induced by laser irradiation could block the blood vessels. Meanwhile, the photothermal effect can also cause the degradation of nanomaterials and release chemotherapeutic drugs in the blocked area, thereby continuously inhibit the neovascularization. Furthermore, SU6668 could inhibit the expression of heat shock protein 70 (HSP70), promoting the cell death induced by photothermal effect. In conclusion, the combination of photothermal and chemotherapy drugs provides a novel, effective and safe approach for the treatment of CNV. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] Metal ion-catecholate complexes (MCCs) extensively exist in plants and animals, which are in charge of versatile biological functions, such as constructing organs, controlled releasing metal ions and antibacterial. Inspired by this, researchers have exploited various kinds of artificial MCCs, which can serve as structural and functional synthons to construct advanced materials. In terms of the structural contribution, these complexes exhibit not only physical interactions, including metal-coordination, hydrogen bonding, π-π stacking and cation-π interactions, but also rich chemical reactions, including radical polymerization, Schiff base reaction and Michael addition. In terms of functional contribution, the complexes can endow the materials with the intrinsic properties of polyphenols and metal ions, including antioxidant, adhesion, antibacterial, bioimaging and catalyst. In addition, some emerging and fantastic functions are also originally from the complexes, such as tunable mechanical property, self-healing, controlled release and photothermal effect. In this review paper, we comprehensively discuss the recent development of MCC-based materials, including coatings, particles, metallogels and metal–organic frameworks (MOFs). Perspectives in this field has also been put forward as well. [ABSTRACT FROM AUTHOR]