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Photo‐ATRP technique has garnered significant attention due to its multitude of advantages, including its ability to be conducted under mild reaction conditions, user‐friendly nature, and exceptional efficiency in polymerization. The heterogeneous photocatalysts not only exhibit exceptional quantum efficiency, but also possess a versatile bandgap that can be finely adjusted to accommodate a wide range of absorption wavelengths within the visible light spectrum, thereby emphasizing their potential for efficient recovery and reuse. The utilization of a variety of heterogeneous photocatalysts in photo‐ATRP presents notable benefits for numerous applications, such as the lack of any remaining substances, simplicity in usage, and potential for reuse. This review focuses on recent progress in photo‐ATRP utilizing a wide variety of heterogeneous photocatalysts, encompassing metal semiconductor nanoparticles, quantum dot, upconversion nanoparticles, metal–organic frameworks, covalent–organic frameworks, conjugated microporous polymers, hypercrosslinked polymer, and carbon‐based materials. [ABSTRACT FROM AUTHOR]

Electrical and electronic equipment (EEE) have revolutionized our lives, however, their associated waste (WEEE) presents a global challenge because at this time EEE relies heavily on metals that are not commonly found in the living environment (Biosphere), which find their way into the environment during both production/disposal of EEE/WEEE. The use of organic components in EEE is increasingly common, particularly with the growing interest in flexible electronics. Here we describe an approach to device design employing in silico toxicity screening to assess the toxicity of the components chosen for use in EEE that is exemplified using inorganic and organic components known in the literature for the production of prototype organic light‐emitting electrochemical cells. This approach could easily be employed to screen a variety of components for which datasets to produce safety data sheets (SDSs) don't yet exist because they have not been produced in large scale or in a regulatory environment which necessitates this. The approach has significant potential to improve high throughput screening of components for EEE that are "safe‐by‐design", potentially in combination with AI and ML approaches. [ABSTRACT FROM AUTHOR]

Photomodulable fluorophores constitute advanced materials as they possess the ability to modify their photophysical properties upon photoirradiation. A new mechanism of photoconversion is recently established, called Directed Photooxidation Induced Conversion based on the coupling of fluorophores with Aromatic Singlet oxygen Reactive Moieties (ASORMs). In this work, The Directed Photooxidation Induced Conversion (DPIC) mechanism is intended to be applied to Perylene BisImide (PBI) due to its appealing photophysical properties. The experimental results showed that coupling two ASORMs to the PBI core, here furan and pyrrole, led to impressive photomodulable fluorophores. While PBI‐F exhibited a photoconversion of 100 nm shift, PBI‐P displayed an 80‐fold fluorescence intensity enhancement upon photoactivation. Analysis of the photoproducts showed that the conversion do not involve an addition of singlet oxygen on the ASORM. Instead, photoconversion occurred through efficient successive photocyclizations. Finally, intracellular vesicles are successfully photoconverted by means of endocytosed PLGA‐polymer nanoparticles loaded with PBI‐F. This study highlights the unique capability of furan‐ and pyrrole‐conjugated fluorophores to enable advanced optical materials with phototransformation properties. [ABSTRACT FROM AUTHOR]

Anthracene based phenoxyl diradicaloids are synthesized. The UV–vis spectra of them give absorption maxima around 700 nm attributes to the extended quinone structure. The diradical characters y of them are estimated as ∼0.6 from their static magnetic susceptibility and absorption maxima. The extended π‐conjugated anthracene‐linker enhances the diradical characters compared to the phenylene linker. It is noteworthy that these enhanced diradical characters are accomplished without steric effects. [ABSTRACT FROM AUTHOR]

Poly[(thiophene)‐alt‐(6,7‐difluoro‐2(2‐hexyldecyloxy)quinoxaline)] (PTQ10) emerges as a promising candidate for donor materials in organic solar cells (OSCs) due to its high efficiency, simplified synthesis, and cost‐effectiveness. The acceptor unit of PTQ10 is derived from the alkylation of 5,8‐dibromo‐6,7‐difluoroquinoxaline‐2‐ol, emphasizing the importance of its economical synthesis for commercial viability. This study investigates triflic acid‐assisted regioselective bromination of quinoxaline derivatives and proposes an alternative synthetic pathway for PTQ10. The developed route benefits from concise synthetic steps, a dependable procedure, and high overall yield. Starting with the condensation of 4,5‐difluorobenzene‐1,2‐diamine with ethyl oxoacetate to yield 6,7‐difluoroquinoxaline‐2‐ol, subsequent triflic acid‐assisted regioselective bromination produces 5,8‐dibromo‐6,7‐difluoroquinoxaline‐2‐ol in high yield. Alkylation under Mitsunobu reaction conditions yields 5,8‐dibromo‐6,7‐difluoro‐2‐(2‐hexyldecyloxy)quinoxaline, followed by polymerization with 2,5‐distannylated thiophene under Stille reaction conditions to afford PTQ10. This research provides insights into efficient synthetic strategies for PTQ10, advancing its potential for commercial application in OSCs. [ABSTRACT FROM AUTHOR]

In this study, the synthesis and characterization of the fluorescent metal–organic framework (MOF)‐polymer composites is reported based on zirconium‐based MOFs (UiO‐66 and UiO‐66(OH)₂) and a conjugated polyelectrolyte, poly(phenylene ethynylene) carboxylate (PPE‐CO₂‐108). The defect‐rich nature of these Zr‐MOFs facilitates strong interactions between the polyelectrolyte's carboxylic acid moieties and the open metal sites on the Zr clusters within the MOF nanoparticles. The composites are prepared by a simple impregnation approach, where MOF nanocrystals suspended in HEPES buffer are added to the polymeric solution under sonication for 10 min. The obtained MOF composites (i.e., UiO‐66‐CPE and UiO‐66 (OH)2‐CPE) are characterized using powder X‐ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer‐Emmett‐Teller (BET) surface area, zeta potential measurements, and UV–vis spectroscopy. The characterization confirmed the homogeneous distribution of the MOF nanocrystals on the polymer as seen in the SEM images, and the interaction with PPE‐CO₂‐108 is confirmed by the decrease in the surface areas from 1050 to 590 m2 g−1 for UiO‐66‐CPE and from 500 to 137 m2 g−1, for UiO‐66(OH)2‐CPE. Fluorescence microscopy revealed strong fluorescence in the microparticles, confirming robust polymer‐MOF interaction. The composites also exhibit improved photostability of the conjugated polyelectrolyte, suggesting their potential for applications in biomedical imaging and other areas requiring stable and bright fluorescent systems. [ABSTRACT FROM AUTHOR]

The New Journal of Chemistry, published by The Royal Society of Chemistry and the Centre National de la Recherche Scientifique, is a scientific journal that aims to connect the world with the chemical sciences. The contents list for the September 21, 2024 issue includes a variety of articles and papers on topics such as the synthesis of nanomaterials, nonlinear optical crystals, and the detection of formaldehyde. The journal provides recognition and professional development opportunities for scientists. Some specific papers in this issue cover the preparation of superhydrophobic/superhydrophilic sodium alginate aerogels for oil absorption, improved efficiency of quantum dot-sensitized solar cells, and the electrocatalytic activity of nickel-doped manganese oxide nanorods. Other topics include the synthesis of nanocomposites for supercapacitor performance, the selective adsorption and photodegradation of residual norfloxacin in water, and the targeted delivery of ifosfamide for cancer treatment. [Extracted from the article]

In this study, we present a pioneering approach for the electrochemical detection of levofloxacin (LVO) in human blood serum utilising iron vanadate nano-bulbs FeVO4 (FVO) decorated on a two-dimensional conjugated polymer matrix g-C3N4 (CN). The iron vanadate nano-bulbs are synthesised via a simple hydrothermal approach and integrated into a 2D conjugated polymer matrix, providing a high surface area and numerous active sites for improved sensing of LVO with a detection limit of 0.06 μM, a broader linear range of 0.25–320 μM, and high sensitivity and selectivity towards LVO. The findings highlight the significant role of vanadium in electrocatalysis, unveiling the sensor's enhanced electrochemical properties and repeatability, reproducibility and stability. This work underscores the potential of FVO nano-bulbs in developing efficient and sensitive electrochemical sensors for pharmaceutical monitoring, providing a valuable tool for real-time drug toxicity analysis. [ABSTRACT FROM AUTHOR]

The thermal conductivity (κ) governs how heat propagates in a material, and thus is a key parameter that constrains the lifetime of optoelectronic devices and the performance of thermoelectrics (TEs). In organic electronics, understanding what determines κ has been elusive and experimentally challenging. Here, by measuring κ in 17 π‐conjugated materials over different spatial directions, it is statistically shown how microstructure unlocks two markedly different thermal transport regimes. κ in long‐range ordered polymers follows standard thermal transport theories: improved ordering implies higher κ and increased anisotropy. κ increases with stiffer backbones, higher molecular weights and heavier repeat units. Therein, charge and thermal transport go hand‐in‐hand and can be decoupled solely via the film texture, as supported by molecular dynamics simulations. In largely amorphous polymers, however, κ correlates negatively with the persistence length and the mass of the repeat unit, and thus an anomalous, albeit useful, behavior is found. Importantly, it is shown that for quasi‐amorphous co‐polymers (e.g., IDT‐BT) κ decreases with increasing charge mobility, yielding a 10‐fold enhancement of the TE figure‐of‐merit ZT compared to semi‐crystalline counterparts (under comparable electrical conductivities). Finally, specific material design rules for high and low κ in organic semiconductors are provided. [ABSTRACT FROM AUTHOR]

Solar‐driven photocatalytic oxygen reduction is a promising pathway for sustainable hydrogen peroxide (H2O2) production. However, limited O2 diffusion and low selectivity in the two‐electron oxygen reduction reaction hinder its practical application. Here, a novel conjugated organic polymer material (conjugated triazine‐thiophene polymer, CTTP) based on triazine and thiophene, integrating a favorable mass transfer structure with competent catalytic centers is presented for the first time. Remarkably, under the gas–liquid–solid triphase condition, the self‐floating CTTP can rapidly capture gaseous oxygen, reducing it to superoxide radicals and transferring them to the reaction interface, drastically enhancing H2O2 yield. An excellent H2O2 concentration of 1.85 mm g−1 h−1 is achieved in a triphase system, representing a remarkable 14‐fold improvement compared to the liquid and solid phase reaction. Interestingly, the triphase system based on CTTP demonstrates the potential for large‐scale H2O2 production under 8 h of sunlight irradiation, reaching 293 ppm day−1 m−2. This work opens up a new avenue for the construction of sustainable H2O2 production systems and may stimulate future related research. [ABSTRACT FROM AUTHOR]

Non‐conjugated luminescent polymers have received much attention due to their excellent flexibility, processability, and biocompatibility. However, the single emission color and low solid‐state luminescence efficiency restrict their further development. Herein, by introducing carboxyl‐terminated alkyl chains on the rigid and helical polymaleimide backbone, a series of non‐conjugated luminescent polymers are designed and synthesized. Due to the "spring lock" formed by the synergism of scalable helical main chains and flexible alkyl side chains, these polymers exhibit effective cluster luminescence with thermally activated delayed fluorescence (TADF) property, thereby significantly improving the solid‐state luminescence efficiency with the quantum yield up to 59.6%. The TADF emission wavelengths of the polymer powders can be tuned from 498 to 639 nm through changing reaction solvents, because the conformation of helical chains forming clusters is sensitive to solvent polarity. Interestingly, metal ions can induce the polymers to construct self‐repairing cluster luminescence gels, which show excellent potential applications in ammonia detection and information encryption. This work not only provides an effective design strategy for the colorful cluster luminescence with high‐efficiency TADF, but also further reveals the cluster luminescence mechanism and enlightens the promising applications of cluster luminescent gels. [ABSTRACT FROM AUTHOR]

This study describes the formation of single‐chain polymer dots (Pdots) via ultrasonic emulsification of nonionic donor‐acceptor‐donor type (D–A–D) alkoxy thiophene–benzobisthiadiazole‐based conjugated polymers (Poly BT) with amphiphilic cetyltrimethylammonium bromide (CTAB). The methodology yields Pdots with a high cationic surface charge (+56.5 mV ± 9.5) and average hydrodynamic radius of 12 nm. Optical characterization reveals that these Pdots emit near‐infrared (NIR) light at a maximum wavelength of 860 nm owing to their conjugated polymer backbone consisting of D–A–D monomers. Both colloidal and optical properties of these Pdots make them promising fluorescence emissive probes for bioimaging applications. The significant advantage of positively charged Pdots is demonstrated in diffusion‐limited mediums such as tissues, utilizing human epithelial breast adenocarcinoma, ATCC HTB‐22 (MCF‐7), human bone marrow neuroblastoma, ATCC CRL‐2266 (SH‐SY5Y), and rat adrenal gland pheochromocytoma, CRL‐1721 (PC‐12) tumor spheroid models. Fluorescence microscopy analysis of tumor spheroids from MCF‐7, SH‐SY5Y, and PC‐12 cell lines reveals the intensity profile of Pdots, confirming extensive penetration into the central regions of the models. Moreover, a comparison with mitochondria staining dye reveals an overlap between the regions stained by Pdots and the dye in all three tumor spheroid models. These results suggest that single‐chain D–A–D type Pdots, cationized via CTAB, exhibit long‐range mean free path of penetration (≈1 µm) in dense mediums and tumors. [ABSTRACT FROM AUTHOR]

A two‐dimensional (2D) conjugated microporous polymer with a structure of 2D nanosheets has been synthesized. Theoretical calculations and experimental results reveal that the Fermi level of this 2D polymer aligns well with perovskite absorber, and its conduction band is high enough to block electron transport into the anode. This 2D polymer is used to modify the hole transport layer, significantly improving its photoelectric properties, including enhanced hole mobility, matched energy level, and reduced recombination. Furthermore, the 2D polymer exhibits a mesoporous structure, allowing perovskite to fill into its loose framework, increasing the hole export area and providing a large hole transport flux. As a result, the efficiency of inverted perovskite solar cells enhances to 24.64 % from 21.17 % of control device without 2D conjugated microporous polymer. Given that this material can be synthesized on a large scale, this work has significant implications for the future development of 2D polymers in perovskite solar cells, potentially accelerating industrialization. [ABSTRACT FROM AUTHOR]

The control of the performance of single-walled carbon nanotube (SWCNT) random network-based transistors is of critical importance for their applications in electronic devices, such as complementary metal oxide semiconducting (CMOS)-based logics. In ambient conditions, SWCNTs are heavily p-doped by the H2O/O2 redox couple, and most doping processes have to counteract this effect, which usually leads to broadened hysteresis and poor stability. In this work, we coated an SWCNT network with various common polymers and compared their thin-film transistors' (TFTs') performance in a nitrogen-filled glove box. It was found that all polymer coatings will decrease the hysteresis of these transistors due to the partial removal of charge trapping sites and also provide the stable control of the doping level of the SWCNT network. Counter-intuitively, polymers with electron-withdrawing functional groups lead to a dramatically enhanced n-branch in their transfer curve. Specifically, SWCNT TFTs with poly (vinylidene fluoride) coating show an n-type mobility up to 61 cm2/Vs, with a decent on/off ratio and small hysteresis. The inverters constructed by connecting two ambipolar TFTs demonstrate high gain but with certain voltage loss. P-type or n-type doping from polymer coating layers could suppress unnecessary n- or p-branches, shift the threshold voltage and optimize the performance of these inverters to realize rail-to-rail switching. Similar devices also demonstrate interesting antiambipolar performance with tunable on and off voltage when tested in a different configuration. [ABSTRACT FROM AUTHOR]

Ordered Ag@Au hybrid nanotube arrays were prepared by a galvanic replacement reaction and subsequently evaluated for their effectiveness as substrates for enhancing the fluorescence of poly(3-hexylthiophene) (P3HT). Ordered AgNWs arrays were assembled using a three-phase interface method, and ordered Ag@Au hybrid nanotube arrays were successfully prepared by a galvanic replacement reaction between a HAuCl4 solution and ordered AgNWs arrays. The morphology of the ordered silver nanowires (AgNWs) arrays and Ag@Au nanotube arrays, as well as the influence of reaction time on the galvanic replacement reaction, were investigated. The fluorescence and laser-Raman properties of the conjugated polymer P3HT on various ordered Ag@Au nanotubes were analyzed. Gold (Au) particles grow on the surface of AgNWs, the diameter of the nanotubes gradually increases, and the ordered Ag@Au hybrid nanotubes form gradually. The surface plasmon resonance (SPR) peaks of Ag@Au hybrid nanotube arrays redshift and become wider as the reaction proceeds compared to AgNW arrays. The fluorescence properties of P3HT films on various ordered Ag@Au hybrid nanotubes were much higher than those on bare silicon substrates, but compared to the gold nanowire array, there is a decrease. As the galvanic displacement reaction progresses, the degree of reduction in fluorescence intensity increases. The unique aspect of this work was that the plasmon resonance wavelength of the ordered Ag@Au hybrid nanotube arrays showed a substantial redshift and broadening, which is much closer to biological samples. The ordered Ag@Au hybrid nanotube arrays can be used as ultra-sensitive fluorescence sensing platforms. [ABSTRACT FROM AUTHOR]

Stretchable organic photovoltaics (OPVs) are pivotal for advancing conformable electronics, yet achieving both efficient and intrinsically stretchable OPVs remains a significant challenge. The main issue is maintaining electronic and mechanical properties under deformation. Here, a ternary blend system, PTzBI‐oF:PYIT:EVA is presented, incorporating ethylene‐vinyl acetate (EVA) to establish a conjugated and elastomeric dual‐network morphology. The elastomer network dissipates applied stress, preserving the crystalline packing of the conjugated network and enabling improved mechanical stability of charge carrier generation and transport. Specifically, with 15% EVA content, the ternary blend achieved a power conversion efficiency (PCE) of 15.28% in rigid devices and exhibited a crack onset strain of 17.23%. Notably, the stretchable OPVs retained over 80% of their initial PCE under 30% strain. These findings underscore the potential of conjugated and elastomeric dual‐network morphology in developing high‐performance stretchable electronics for various applications. [ABSTRACT FROM AUTHOR]

[Display omitted] The diversity of catalytic products determines the difficulty of selective product modulation, which usually relies on adjusting the catalyst and reaction conditions to obtain different main products selectively. Herein, we synthesized D-π-A-D conjugated organic polymers (TH-COP) using cyclotriphosphonitrile, alkyne, 2H-benzimidazole, and sulfur units as electron donors, π bridges, electron acceptors, and electron donors, respectively. TH-COP exhibited excellent photoinduced carrier separation and redox ability under different visible light wavelengths, and the main products of its CO 2 reduction are CH 4 (1000.0 μmol g−1) and CO (837.0 μmol g−1) under 400–420 nm and 420–560 nm, respectively. In addition, TH-COP could completely convert phenylmethyl sulfide to methyl phenyl sulfone at 400–420 nm and diphenyl disulfide at 480–485 nm in yields up to 95 %. This study presents a novel strategy for the targeted fabrication of various main products using conjugated polymers by simply changing the wavelength range of visible light. [ABSTRACT FROM AUTHOR]

Pathogenic bacteria are closely associated with the occurrence, development and metastasis of oral squamous cell carcinoma (OSCC). Antibacterial therapy has been considered an enhancement strategy to suppress bacteria-associated tumors and promote anti-tumor immune responses. Herein, we developed an injectable adhesive hydrogel, PNIPAM/DL@TIR, for the in situ photothermal ablation and robust stimulation of antitumor immunity against OSCC colonized by Porphyromonas gingivalis (Pg), one of the major oral pathogenic bacteria. PNIPAM/DL@TIR, composed of poly(N-isopropylacrylamide), demethylated lignin, and TAT peptide-conjugated IR820, was prepared using a simple dissolve-dry-swell solvent exchange method. Upon 808 nm laser irradiation, PNIPAM/DL@TIR exerted photothermal effects to ablate Pg-colonized OSCC and generate dual tumor and bacterial antigens. Owing to its large number of catechol groups, PNIPAM/DL@TIR efficiently captured these antigens to form an in situ antigen repository, thereby eliciting robust and durable antitumor immune responses. Proteomic analysis revealed that the captured antigens comprised both tumor neoantigens and bacterial antigens. The catechol groups endowed PNIPAM/DL@TIR with antioxidant activity, which was also conducive to stimulating antitumor immunity. Altogether, this study develops an injectable adhesive hydrogel and provides a combination strategy for treating bacteria-associated OSCC. In this study, we developed an injectable adhesive hydrogel, PNIPAM/DL@TIR, for in situ photothermal ablation and robust stimulation of antitumor immunity against OSCC colonized by Porphyromonas gingivalis , one of the major oral pathogenic bacteria. PNIPAM/DL@TIR, which consists of poly(N-isopropylacrylamide), demethylated lignin, and TAT peptide-conjugated IR820 exhibited outstanding photothermal performance. Owing to the presence of catechol groups, PNIPAM/DL@TIR has good bioadhesive properties and can capture protein antigens to form in situ antigen repository, thus initiating robust and long-term antitumor immune responses. In addition, PNIPAM/DL@TIR exhibited strong antioxidant activity that is favorable for promoting antitumor immunity. In the mouse model of OSCC with bacterial infection, PNIPAM/DL@TIR not only ablated the primary tumors upon NIR laser irradiation, but also induced tumor and bacterial vaccination in situ to suppress distant tumors and lung metastasis. [Display omitted] [ABSTRACT FROM AUTHOR]

Multiscale structural evolution of conjugated polymer (CP) solutions from disorder to aggregation via environmental perturbations is a universal phenomenon in condensed matter physics. Here, we take poly(3‐hexylthiophene‐2,5‐diyl) (P3HT) as a model material and use Ultraviolet–Visible (UV–Vis) spectroscopy to study the hierarchical structure evolution during prolonged aging at relatively low temperature. Using in‐situ UV–Vis spectroscopy and the Franck‐Condon (FC) method, the dynamics of multiscale structural transitions in P3HT were elucidated. Hierarchical structural details can be extracted from the UV–Vis spectra, including the overall percentage of aggregates, conjugation length, degree of H‐/J‐type molecular packing, and site energetic disorder. Through covariance analysis of conformational disorder to aggregation transitions of conjugated polymers obtained under multiple conditions, we find that the trends of the above four key parameters are not consistent, which informs the unique evolution of the degree of ordering at different length scales within the aggregates. This work facilitates the scrutiny of the hierarchical structural transition from multi‐length scale perspective. [ABSTRACT FROM AUTHOR]

A poly(para)phenylene conjugated polymer is developed to store information via a quick and facile optical writing method. After exposure to UV light, co‐fluorescence (films with two or more written emission colors –, i.e., "double‐on") and "on‐off" states are written into the flexible polymer films. The hidden information is invisible under ambient lighting and can only be read with an appropriate light source, optical filter, and/or magnifier, thus providing a level of security for information encoded into the films. The physical and chemical mechanisms are discussed responsible for the rapid fluorescence changes that occur under UV exposure and demonstrate microscale multi‐colored artwork and hidden QR codes written into pliable and freestanding films. Depending on the preparation, the written patterns remained easily visible and stable after exposure to water and to ambient levels of UV background radiation. [ABSTRACT FROM AUTHOR]

The nature of interchain π-system contacts, and their relationship to hole transport, are elucidated for the high-mobility, noncrystalline conjugated polymer C16-IDTBT by the application of scanning tunneling microscopy, molecular dynamics, and quantum chemical calculations. The microstructure is shown to favor an unusual packing motif in which paired chains cross-over one another at near-perpendicular angles. By linking to mesoscale microstructural features, revealed by coarse-grained molecular dynamics and previous studies, and performing simulations of charge transport, it is demonstrated that the high mobility of C16-IDTBT can be explained by the promotion of a highly interconnected transport network, stemming from the adoption of perpendicular contacts at the nanoscale, in combination with fast intrachain transport. [ABSTRACT FROM AUTHOR]

AbstractNanodiamonds have been researched as sphere-shaped carbon nano-entities having countless surface/structural properties, facile fabrication and mammoth technological value. An important utilization of nanodiamonds has been observed as nano-reinforcing agents for nanocompositing purposes. Semiconducting polymers (conjugated polymers) having π electron delocalization have been documented for worthy electrochemical/optical/thermal/mechanical features, in addition to the electron transfer through their backbone. Doping of carbonaceous nanoparticles, like nanodiamonds, with conjugated polymers have been found to further improve the valuable physical characteristics in their final nanocomposite form. Correspondingly, this overview describes the impact of nanodiamond nano-reinforcement on the specialized aspects of polyaniline/nanodiamond, polypyrrole/nanodiamond and polythiophene/nanodiamond nanocomposites. According to literature reports, these groupings of conjugated polymer/nanodiamond hybrids revealed noteworthy microstructural, conductive, optical, electrochemical, microwave absorption, specific capacitance, photovoltaic and actuation characteristics. Subsequently, several significant applications of polymer/nanodiamond nanomaterials have been explored including the solar cells, supercapacitors and actuators. [ABSTRACT FROM AUTHOR]

We report a bioinspired approach to tune surface nanostructures by soft‐template electropolymerization in micellar conditions. Monomers highly favoring π‐stacking interactions are particularly interesting for favoring the polymer deposition in one direction. Here, original triphenylamine‐based monomers di‐substituted by thiophene and carbazole are investigated. Conjugated building blocks monomers are tested to favor deposition vs polymerization, even if the monomers are not perfectly planar. The carbazole derivatives have a much higher electrodeposition capacity than the thiophene derivatives, which is unexpected if thiophene and carbazole are taken alone. Moreover, in all electrodeposited films, monomer seems to be present as shown by cyclic voltammetry experiments, confirming previous works. The amount of monomer vs oligomers is highly dependent on the investigated monomer. For the resulting surface structures, hollow spheres and nanoribbons are particularly formed with some investigated monomers by cyclic voltammetry while nanotubes are observed at constant potential. The formation of nanotubes indicates a polymer growth more favored in one direction. These surfaces are less hydrophobic (water contact angle up to 111.5°) compared to films with spherical nanoparticles but these results can be explained only by the presence of air inside the surface roughness. [ABSTRACT FROM AUTHOR]

Heterocyclic organic semiconductors have attracted significant attention as photocatalysts for hydrogen evolution due to excellent absorbency and abundant active sites. Herein, we developed a dual heterocyclic (O/S) conjugated microporous polymer Py-Th-Fu, consisting of both the furan and thiophene heterocycles, for photocatalytic H 2 evolution. Compared with the furan O-heterocycle Py-Fu and thiophene S-heterocycle Py-Th, the Py-Th-Fu with the dual heterocyclic structure is more outstanding in regulating the optoelectronic properties, morphological properties, electric charge shift kinetics, and photocatalytic H 2 evolution activity. Computational analysis also elucidates the smallest hydrogen adsorption free energy of Py-Th-Fu, which suggests it is the most advantageous for hydrogen mass transfer in this dual heterocycle polymer. As a result, the synergistic combination of two different heteroatom catalytic sites enables the dual heterocycle Py-Th-Fu to afford enhanced catalytic activity with an optimal rate of 23.28 mmol g−1 h−1, which is nearly equal to 5.06 and 1.58 times that of the corresponding O- and S-containing single heterocycles Py-Fu and Py-Th under visible lighting (λ > 420 nm). Our study demonstrates that the dual heterocyclic strategy using ternary copolymerization to tune the optoelectronic properties may open the horizon for fabricating high-performance photocatalytic water splitting via sunlight-driven hydrogen evolution. [Display omitted] • We developed a CMP photocatalyst with double heterocyclic strategy. • This strategy regulated the morphological properties and charge transfer kinetics. • Double heterocycle exhibited better HER than the single heterocycle in CMPs. [ABSTRACT FROM AUTHOR]

Fully π-conjugated polymers with rigid aromatic units are promising for flexible optoelectronic devices, but their inherent brittleness poses a challenge for achieving high-performance, intrinsically stretchable fully π-conjugated polymer. Here, we are establishing an external-plasticizing strategy using semiconductor fluid plasticizers (Z1 and Z2) to enhance the optoelectronic, morphological, and stretchable properties of fully π-conjugated polymer films for flexible light-emitting diodes. The synergistic effect of hierarchical structure and optoelectronic properties of Z1 in poly(9,9-di-n-octylfluorene-alt-benzothiadiazole) (F8BT) films enable excellent stretchable deformability (~25%) and good conductivity. PLEDs based on F8BT/Z1 films show stable electroluminescence and efficiency under 15% stretch and 100 cycles at 10% strain, revealing outstanding stress tolerance. This strategy is also improving the stretchable properties of polymers like poly(9,9-di-n-octylfluorenyl-2,7-diyl) (PFO) and poly(2-methoxy-5(2′-ethyl)hexoxy-phenylenevinylene) (Super Yellow), demonstrating its general applicability. Therefore, this strategy can provide effective guidance for designing high-performance stretchable fully π-conjugated polymers films for flexible electronic devices. The realization of intrinsically stretchable fully π-conjugated polymer film is challenging due to their inherent brittle nature. Here, authors apply semiconductor fluid molecular plasticizers to improve stretchable deformability, achieving high performance flexible polymer light-emitting diodes. [ABSTRACT FROM AUTHOR]

The significant interfacial resistance between solid electrolyte‐electrode interfaces is a major bottleneck for the practical application of solid‐state lithium batteries. This resistance is primarily caused by the formation of space charge layers (SCLs), resulting from the redistribution of ionic carriers at the interface between dissimilar materials with varying chemical potentials, which lead to insufficient carriers and sluggish lithium‐ion transport. In this study, a conjugated structure polymer is constructed through in situ polymerization onto the oxide electrolyte, forming charge‐rich SCLs on the organic/inorganic interface, and enabling the interfacial layer to maintain superior ion transfer and contact. The Li solid NMR spectra and computational study suggest that optimized SCLs offer effective pathways for Li+ conduction in the electrolyte, thereby enhancing the interfacial conduction. Furthermore, the designed electrolyte induces the formation of an inorganic‐rich interphase layer on the lithium anode, enabling rapid lithium‐ion transport and uniform Li deposition. Consequently, the lithium symmetric cell with this electrolyte operates for more than 5100 h, while LiFePO4/Li solid‐state batteries can stably cycle up to 800 times at 5 C. This interfacial modification strategy provides a new perspective for the rational design of the charge‐rich SCLs and advances the understanding of the SCLs inside the electrolyte. [ABSTRACT FROM AUTHOR]

Low efficiency of photogenerated electron–hole separation has been a challenge for organic conjugated polymer photocatalysts. Our preceding studies have revealed that polymers containing B←N coordination bonds can form a localized built-in electric field that effectively promotes photogenerated charge separation. However, B←N coordination units are still scarce and require more examples to find regularities in their structural design. The systematic development and testing of B←N coordination units is necessary for the efficient development of subsequent polymers containing B←N coordination bonds. In this work, three conjugated polymers containing B←N coordination bonds, PBN–Ni, PBP–Ni, and PBS–Ni, were synthesized by changing the substituents of the boron atoms and introducing narrow-band thiophene units to form conjugate and energy band gradients. The energy band modulation and localized built-in electric field construction were both achieved as planned, while the bandgap and photogenerated charge transport capabilities caused performance discrepancies. The experimental results showed that PBN–Ni had a better photocatalytic hydrogen evolution (HER) performance, reaching 104.6 μmol h−1 (λ > 420 nm). The optimal optical absorption edge of PBS–Ni was up to 643 nm, but the HER was lower, at 33.2 μmol h−1 (λ > 420 nm, 1% Pt). PBP–Ni optimized some of the optical absorption efficiencies (511 nm) while ensuring the HER activity (96.6 μmol h−1, λ > 420 nm). This work tentatively explores the characterization of the B←N coordination bond-containing base units serving as photocatalysts and provides the basic model experience and data reference for the subsequent expansion of B←N coordination bond-containing units and the development of B←N coordination bond-containing copolymer systems. [ABSTRACT FROM AUTHOR]

We present a novel synthetic route for the rapid construction of dithieno[3′,2′:3,4;2′′,3′′:5,6]benzo[1,2‐c][1,2,5]thiadiazoles via Na2S‐promoted thiophene annulation. This method facilitated the synthesis of D18−Cl polymer, known for its efficacy as a polymer donor in bulk‐heterojunction polymer solar cells. Starting from commercially available 4,7‐dihalo‐5,6‐difluorobenzo[c][1,2,5]thiadiazole, various 4,7‐dialkynylated compounds were obtained through Sonogashira reaction conditions. Subsequent Na2S‐promoted thiophene annulations yielded DTBT and its derivatives in excellent yields within 10 minutes. DTBT was then utilized as a precursor for the concise synthesis of D18−Cl, benefiting from reduced synthetic steps, mild reaction conditions, decreased complexity, and high overall yields. In another route, a space group‐bridged DTBT was directly constructed via Na2S‐promoted thiophene annulations and converted into D18−Cl through a couple of steps. This developed protocol offers a straightforward and reliable synthetic tool, conducive to reducing complexities in the production of DTBT‐based organic electronic materials, thereby advancing the potential commercialization of organic solar cells. [ABSTRACT FROM AUTHOR]

This account summarizes the impact that the quest for sustainability is having on the field of organic polyconjugate molecules and polymers for plastic (opto)electronics. While at the proof-of-concept level, the design criteria as well as the preferred synthetic strategies to access new and improved materials have been dominated by the need for performance. The ongoing transition from the lab environment to the industrial scale imposes strict limitations on the cost and overall environmental impact of new materials. We here summarize our efforts on the development of new design criteria and synthetic strategies aimed at improving sustainability – without compromising performance – in organic polyconjugated molecules. The article is composed of three sections: Introduction and motivation, sustainability through improved synthetic methods and through improved design. Outline 1 Introduction and Motivation 2 Sustainable Reaction Methods 2.1 The New Tools: Reactions in Aqueous Solution of Surfactants 2.2 Intrinsically More Sustainable Reactions: Direct Arylation 2.3 Sustainable Multistep Protocols: Combining Micellar, Solventless, and Mechanochemical Methods 3 Sustainability as a Design Criterion: De Novo Design 4 Conclusion [ABSTRACT FROM AUTHOR]

Photocatalytic hydrogen evolution has attracted tremendous interest as it offers a process for generation of green hydrogen based on solar radiation. But the process is extremely complex as many factors influence photocatalytic hydrogen evolution. While novel photocatalysts such as MOFs, perovskites, conjugated polymers, carbon-based materials, quantum dots, and others face challenges such as stability and scalability, semiconductor photocatalysts and cocatalysts such as TiO 2 /Pt, Ni–CdS, CdS/ZnO, CdS/ZnS have the advantages of simplicity in synthesis, stability, and scalability. Despite decades of research, challenges such as charge separation, spectrum usage, low hydrogen generation efficiency, photocatalyst stability and scalability persist. This review discusses what has been achieved so far in the domain of photocatalytic hydrogen evolution and presents a critical analysis of challenges to be addressed in developing a robust and practical photocatalytic hydrogen generation system based on efficiency of photocatalysts and their stability and the extreme importance of efficient reactor designs. [Display omitted] • Challenges associated with photocatalytic hydrogen generation systems. • Photocatalysts, cocatalysts and their stability challenges in hydrogen evolution. • Potential of semiconductor nanostructures, plasmonic nanoparticles and QDs. • Importance of reactor designs in enhancing photocatalytic hydrogen evolution. [ABSTRACT FROM AUTHOR]

[Display omitted] Two novel conjugated polymers comprised of 2,3-R 2 -di- thieno[3,2- f :2 ' ,3 ' - h ]quinoxaline, where R is 3 ' -(octyloxy)- phenyl (P1) or 2 ' -(2-ethylhexyl)thiophen-4 ' -yl (P2), and 2,1,3-benzothiadiazole have been synthesized using the Stille cross-coupling reaction. The synthesized polymers were investigated as hole transport layer (HTL) materials in perovskite solar cells. Polymer P2 as an HTL material provided improved short-circuit current and open-circuit voltage and, correspondingly, enhanced power conversion efficiency of perovskite solar cells compared to that of polymer P1. [ABSTRACT FROM AUTHOR]

The advent of nonfullerene acceptors (NFAs) has greatly improved the photovoltaic performance of organic solar cells (OSCs). However, to compete with other solar cell technologies, there is a pressing need for accelerated research and development of improved NFAs as well as their compatible wide bandgap polymer donors. In this study, a novel electron‐withdrawing building block, succinimide‐substituted thiophene (TS), is utilized for the first time to synthesize three wide bandgap polymer donors: PBDT‐TS‐C5, PBDT‐TSBT‐C12, and PBDTF‐TSBT‐C16. These polymers exhibit complementary bandgaps for efficient sunlight harvesting and suitable frontier energy levels for exciton dissociation when paired with the extensively studied NFA, Y6. Among these donors, PBDTF‐TSBT‐C16 demonstrates the highest hole mobility and a relatively low highest occupied molecular orbital (HOMO) energy level, attributed to the incorporation of thiophene spacers and electron‐withdrawing fluorine substituents. OSC devices based on the blend of PBDTF‐TSBT‐C16:Y6 achieve the highest power conversion efficiency of 13.21%, with a short circuit current density (Jsc) of 26.83 mA cm−2, an open circuit voltage (Voc) of 0.80 V, and a fill factor of 0.62. Notably, the Voc × Jsc product reaches 21.46 mW cm−2, demonstrating the potential of TS as an electron acceptor building block for the development of high‐performance wide bandgap polymer donors in OSCs. [ABSTRACT FROM AUTHOR]

With the increasing infection of drug-resistant bacteria, it has become a great challenge for researchers to find new approaches to eradicate drug-resistant bacteria and their biofilms. Photodynamic antimicrobial chemotherapy (PACT) is an indispensable part of the new anti-bacterial strategy because of its unique anti-bacterial mechanism, which can effectively inactivate drug-resistant bacteria without inducing further drug resistance. In this work, nanoparticles with N-isopropylacrylamide and methacryloxyethyltrimethyl ammonium chloride as monomers, and loaded with a fluorescent conjugated polymer were successfully prepared by microemulsion polymerization. The average particle size ranged from 100 to 200 nm. The nanoparticles could disperse in water steadily according to their zeta potential analysis. The nanoparticles generated singlet oxygen upon exposing to light with wavelength of 500–700 nm. Their PACT efficiency was investigated against Escherichia coli, Staphylococcus aureus, and methicillin-resistant Staphylococcus aureus respectively. The results indicated that the antibacterial ability of nanparticles were excellent as the concentration was more than 0.01 mg/mL and the illumination time was 30 min. When the mass concentration of the nanoparticles was equal to or more than 0.05 mg/mL, the antibacterial mechanism was dominated by cation action, and when the concentration was equal or lower than 0.01 mg/mL, the antibacterial ability of the nanoparticles was improved effectively by photodynamic action. The antibacterial rate of the nanoparticle solutions against the bacteria in the biofilm was quantitatively studied, and it was proved that the nanoparticles eliminated bacteria in the biofilm effectively with a nanoparticle concentration of 0.2 mg/mL or more. The results indicated that the nanoparticles could effectively penetrate the biofilm to kill bacteria inside the biofilm by light illumination. [ABSTRACT FROM AUTHOR]

A macromolecule viz; poly (p-phenylene azomethine) (PPAM) has been synthesized by a novel methodology for utilization in opto-electronic devices. The developed PPAM has been comprehensively characterized by using UV-Visible and FTIR techniques. X-ray studies affirmed the crystalline nature of PPAM, while UV-visible absorption spectroscopy, in DMSO, confirmed the extensive conjugation; with promising optical properties. Thermal stability was evaluated through thermogravimetric analysis. The computational analysis of PPAM was also implemented to complement the experimental observations. To explore practical applications, a homogenous film was successfully developed from PPAM with a minor quantity (0.25wt%) of poly(methyl methacrylate) PMMA. The resulting film was characterized for thermal stability, morphological features, and optical behaviour. The findings underscore the potential of PPAM as a versatile material with tunable properties, opening avenues for innovative applications in the realm of optical science. [ABSTRACT FROM AUTHOR]

A viable tactic to effectively address the climate crisis is the production of renewable fuels via photocatalytic reactions using solar energy and available resources like carbon dioxide (CO2) and water. Organic polymer material-based photocatalytic materials are thought to be one way to convert solar energy into valuable chemicals and other solar fuels. The use of porous organic polymers (POPs) for CO2 fixation and capture and sequestration to produce beneficial compounds to reduce global warming is still receiving a lot of interest. Visible light-responsive organic photopolymers that are functionally designed and include a large number of heteroatoms and an extended π-conjugation allow for the generation of photogenerated charge carriers, improved absorption of visible light, increased charge separation, and decreased charge recombination during photocatalysis. Due to their rigid structure, high surface area, flexible pore size, permanent porosity, and adaptability of the backbone for the intended purpose, POPs have drawn more and more attention. These qualities have been shown to be highly advantageous for numerous sustainable applications. POPs may be broadly categorized as crystalline or amorphous according to how much long-range order they possess. In terms of performance, conducting POPs outperform inorganic semiconductors and typical organic dyes. They are light-harvesting materials with remarkable optical characteristics, photostability, cheap cost, and low cytotoxicity. Through cocatalyst loading and morphological tweaking, this review presents optimization options for POPs preparation techniques. We provide an analysis of the ways in which the preparative techniques will affect the materials' physicochemical characteristics and, consequently, their catalytic activity. An inventory of experimental methods is provided for characterizing POPs' optical, morphological, electrochemical, and catalytic characteristics. The focus of this review is to thoroughly investigate the photochemistry of these polymeric organic photocatalysts with an emphasis on understanding the processes of internal charge generation and transport within POPs. The review covers several types of amorphous POP materials, including those based on conjugated microporous polymers (CMPs), inherent microporosity polymers, hyper-crosslinked polymers, and porous aromatic frameworks. Additionally, common synthetic approaches for these materials are briefly discussed. [ABSTRACT FROM AUTHOR]

Polyelectrolytes are charged polymers comprising macromolecules in which substantial portions of the constituent units contain cationic (e.g., pyridinium, ammonium) or anionic (e.g., sulfonate, carboxylate) groups, which possess special functions from the features of counterions, such as dissociation to charged species, mechanical stability, phase behavior, etc. Therefore, functional polyelectrolytes have been widely applied in many fields. In this perspective, we present some progresses in the studies of poly(polyoxometalate)s, denoted as poly(POM)s, as a kind of new charged polymers/polyelectrolytes, by covalent bonding between the inorganic polyoxometalate (POM) clusters and the organic polymer chains. According to the distinct positions of POMs in polymer chain and functions of poly(POM)s, they are divided into the following four categories: crosslinked poly(POM); side-chain poly(POM); backbone poly(POM), including poly(POM)-conjugated polymer hybrid and block poly(POM)-polymer; and POM-based covalent organic framework (PCOF). This perspective introduces the synthesis methods of poly(POM) polyelectrolytes and their macromolecular and aggregate structural characteristics, while also focusing on their properties and functions. Their application areas include catalysis, thermal resistance, optical functions, fuel cells and batteries, etc. [ABSTRACT FROM AUTHOR]

Conjugated polymers (CPs) are widely used as conductive materials in various applications, with their conductive properties adjustable through chemical doping. While doping enhances the thermoelectric properties of CPs due to improved main-chain transport, overdoping can distort the polymer structure, increasing energy disorder and impeding intrinsic electrical transport. This study explored how different dopants affect the structural integrity and electrical transport properties of CPs. We found that dopants vary in their impact on CP structure, consequently altering their electrical transport capabilities. Specifically, ferric chloride (FeCl3)-doped indacenodithiophene-co-benzothiadiazole (IDTBT) shows superior electrical transport properties to triethyloxonium hexachloroantimonate (OA)-doped IDTBT due to enhanced backbone planarity and rigidity, which facilitate carrier transport and lower energetic disorder. These results highlight the critical role of dopant selection in optimizing CPs for advanced applications, suggesting that strategic dopant choices can significantly refine the charge transport characteristics of CPs, paving the way for their industrialization. [ABSTRACT FROM AUTHOR]

How plasmonic nanostructures modulate the behavior of exciplexes and excimers within materials remains unclear. Thus, advanced knowledge is essential to bridge this gap for the development of optoelectronic devices that leverage the interplay between plasmonic and conjugated polymer hybrid materials. Herein, this work aims to explore the role of gold nanoparticles (AuNPs) in modulating exciplex and excimer states within the conjugated polymer poly(2,5-di(3,7-dimethyloctyloxy) cyanoterephthalylidene) (PDDCP), known for its photoluminescent and semi-conductive properties, aiming to create innovative composite materials with tailored optical features. The spectral analysis was conducted to investigate the effects of AuNPs on the PDDCP, varying AuNP volume percentages to measure changes in the absorption profile, molar extinction coefficient (ε), absorption cross-section (σa), and optical bandgap ( E g ). Fluorescence spectra of the mixture at different volume ratios were also examined to assess exciplex formation, while amplified spontaneous emission (ASE) profiles were analyzed to study the behavior and photochemical stability of the polymer–NP hybrid material. Increasing AuNP volume induced both blue and red shifts in the absorption profile of the PDDCP. Higher AuNPs concentrations correlated with decreased ε and σa, inversely impacting E g . The emission spectra obtained at varied AuNP volume ratios indicated significantly enhanced exciplex and excimer formations. The ASE profiles remained consistent but showed reduced intensity with increasing AuNPs concentrations, indicating their influence on hybrid material behavior and stability. The findings suggest that AuNPs affect PDDCP's optical characteristics, altering the absorption profile, bandgap, and fluorescence spectra. Furthermore, the observed reduction in ASE intensity highlights their influence on the behavior and photochemical stability of the hybrid material. These results contribute to a better understanding of the versatile applications of plasmonic-conjugated hybrid polymers. [ABSTRACT FROM AUTHOR]

The development of intrinsically stretchable polymer semiconductor holds substantial promise in the field of wearable electronics. However, charge transport mobility is typically compromised in existing stretchable semiconductors to achieve the desired stretchability. Herein, a novel "regional conjugation" strategy is proposed to design an intrinsically stretchable polymer semiconductor oligo‐diketopyrrolopyrrole‐thieno[3,2‐b]thiophene (DPPTT)–urethane, in which oligo‐DPPTT conjugated units and alkyl urethane nonconjugated units are introduced. The regional conjugation of oligo‐DPPTT in the polymer backbone endows DPPTT–urethane with good molecular packing, leading to a high mobility of up to 1.7 cm2 V−1 s−1. Additionally, incorporating alkyl urethane nonconjugated units in the backbone can reduce film crystallinity and chain aggregation, which contribute to the stretchability of the polymer thin film. Consequently, fully stretchable transistors retain carrier mobility even at 100% biaxial tensile strain. Furthermore, the fully stretchable organic field‐effect transistor arrays show remarkable charge transport reversibility and durability after 1000 stretch–release cycles at 25% strain. Additionally, the device exhibits extraordinary electrical stability in air atmosphere. Overall, these results indicate that the "regional conjugation" strategy provides an effective and promising methodology to design intrinsically stretchable and high‐performance polymer semiconductor that can advance the development of soft and wearable electronics. [ABSTRACT FROM AUTHOR]

Bio‐inspired by natural species and previous research works, nanotubes are prepared by soft‐template electropolymerization in micellar solution. Various thiophene‐based and carbazole‐based monomers are designed from a triphenylamine core. With one of the carbazole‐based monomers, which is fully conjugated and with a star‐like structure, gecko‐like surface structures are obtained even if the structure is not perfectly planar. Extremely long and densely packed‐microtubes are reached especially at constant potential. However, the surfaces are not both highly hydrophobic and with strong water adhesion, but are superhydrophilic. These wetting properties can be explained by a high surface energy (γSV)=41.9 mN m−1 compared to gecko foot even if the natural gecko feet are also chemically inhomogeneous, or by differences in the arrangement of the surface structures. [ABSTRACT FROM AUTHOR]

π‐Conjugated polyfluorenes (PPs) comprising 2,3‐diaminobenzene‐1,4‐diyl (unit A) and 9,9‐dihexylfluorene‐2,7‐diyl (polymer‐1) or 9,9‐bis(6‐N,N,N,‐trimethylammoniumhexyl)fluorene‐2,7‐diyl (unit B) (polymer‐2) units were synthesized using Suzuki‐Miyaura coupling polycondensation. To compare the chemical properties and functionality of polymer‐2, a water‐soluble PP comprising benzene‐1,4‐diyl and unit B (polymer‐3) was synthesized. Polymer‐1 exhibited solvatochromism: the photoluminescence (PL) peak of the polymer in solutions shifted to a longer wavelength with an increase in the dielectric constants of solvents. Polymer‐1 formed charge transfer (CT) complexes with organic electron acceptors. The CT complexation behavior was systematically elucidated by the PL measurements using Stern–Volmer and Benesi–Hildebrand methods. Water‐soluble polymer‐2 could be used as a sensor for the chain length of telomere DNA by monitoring the changes in its PL intensity upon the addition of the analyte. The DNA sensing performance of polymer‐2 surpassed that of polymer‐3, attributed to the presence of unit A in polymer‐2. This unit brought polymer‐2 closer to DNA through hydrogen bonding between the amino group of polymer‐2 and nucleic acids in DNA. This interaction facilitated the occurrence of CT from the polymer backbone to DNA. [ABSTRACT FROM AUTHOR]

Temperature-responsive drug delivery systems offer the chance to better deliver anti-tumor drugs to tumor cells in a more controllable condition. In this work, a novel temperature-responsive nanocarrier was synthesized by grafting allyl alcohol and N-isopropyl acrylamide onto a nanodiamond surface and conjugated with polyester dendrimer for the controlled delivery of paclitaxel and photo-thermal therapy under near-infrared light irradiation. The morphology, chemical structure, and properties of this polymer were characterized through systematic characterization analyses. The data obtained from the non-linear isotherm model indicated that the sorption procedure followed Langmuir isotherm. Adsorption kinetic data shown that the pseudo-second-order model fitted well with the experimental results. The in-vitro drug release shown that about 92.10% of paclitaxel release was found to be occurred at the simulated physiological fluid within 48 h (pH 7.4; T = 45 °C), whereas about 64.38% of paclitaxel release occurred at the temperature of 37 °C (pH 7.4). Also, the released drug under near-infrared light irradiation reached up to 97.34% over 15 min, achieving the on-demand paclitaxel release. The release of the drug from the nanocarrier followed the mechanism of non-Fickian diffusion and best fitted to the Korsmeyer–Peppas model. The nanocarrier indicated dose dependent cytotoxicity towards MCF-7 cancer cells. [ABSTRACT FROM AUTHOR]

Organic conjugated polymers have received extensive attention due to their unique electronic properties. However, there have been relatively few reports on the dark photocatalytic reactions utilizing organic conjugated polymers. Herein, we report the successful synthesis of an organic conjugated polymer based on poly (heptazine imide) nanocrystals (CNNCs) for H2O2 evolution and biomedical applications using a simple salt molten method and sonication–centrifugation process. The results show that these colloid CNNCs have the characteristics of photogenerated electrons accumulation and realize dark photocatalysis with high reducibility under visible light irradiation. Notably, these accumulating photogenerated electrons can reduce O2 in darkness to produce H2O2. In addition, cytotoxicity tests were conducted and it was found that H2O2 produced under dark conditions could oxidize L-arginine (L-Arg) to NO, which effectively killed tumors in the dark. This work provides an important strategy to construct organic conjugated semiconductor nanocrystals and applying them to future energy and biomedical fields. [ABSTRACT FROM AUTHOR]

The type of aggregation in conjugated polymers determines their use in electronic devices. H-type aggregates are most suitable for solar cell applications, while J-type aggregates are recommended for light-emitting diodes. In this work, we used three methods to determine the type of aggregates in a benzodithiophene–isoindigo-based (PBDTI-DT) copolymer, namely, Huang–Rhys factor evolution with temperature, Franck–Condon analysis, and relative quantum yield (QY) calculation. All three methods indicate that both aggregation types are present, and the QY calculation clearly indicates that H-aggregates are more dominant. Time-dependent density functional theory was used to identify the two absorption bands of PBDTI-DT as local π − π* and intramolecular charge-transfer transitions. [ABSTRACT FROM AUTHOR]

U6N@COP-Ag composites were prepared by covalent bonding and photodeposition. The prepared SPR synergetic Z-Scheme U6N@COP-Ag photocatalyst showed better nitrogen reduction performance without sacrificial agents. [Display omitted] The photocatalytic efficiency can be improved by constructing a Z-scheme heterojunction, but hindered by the only half utilization efficiency of photogenerated carriers. Thus, a novel material, UiO-66-NH 2 @TAPB-BTCA-COP-Ag (U6N@COP-Ag), with surface plasmon resonance (SPR) effect synergistic Z-scheme heterostructure has been prepared by depositing Ag nanoparticles (Ag NPs) on TAPB-BTCA-COP (COP)-coated UiO-66-NH 2. The deposited Ag NPs expand the range of light absorption and introduce more photogenerated electrons in the composite. The SPR effect of noble metal compensates for the limited utilization of the Z-scheme heterojunction photogenerated carriers and the increased density of semiconductor carriers at the reducing end, which is more conducive to the redox reaction of the catalyst. Without sacrificial agents, U6N@COP-Ag shows great photocatalytic nitrogen reduction conversion efficiency with the rate of NH 4 + in ammonia water at 167.63μmol g-1h−1, which is 6.6 and 2.8 times that of the original UiO-66-NH 2 and COP, respectively. In-situ XPS and Kelvin probe technology verify that UiO-66-NH 2 and Ag nanoparticles provide more photogenerated electrons to COP. The cleavage and conversion of N 2 to NH 4 + on U6N@COP-Ag was confirmed by the enhancement of N H bonds and NH 4 + characteristic absorption peaks in the in-situ diffuse reflectance infrared Fourier transform spectroscopy (in-situ DRIFTS). This work presents a great method to improve the Z-scheme heterojunction photogenerated carrier utilization and the density of semiconductor carriers at the reducing end by the noble metal SPR effect, which is more conducive to enhance the redox reaction of the catalyst. [ABSTRACT FROM AUTHOR]

A series of electrochromic π-conjugated polymers which cover almost full-colour gamut are designed. This is the first time to deeply explore the multicolour electrochromic mechanism in this material system. Based on a fine adjustment on their energy level structures, which are further developed into flexible electrochromic prototype devices with dynamic multicolour displays. [Display omitted] Multicolour electrochromic materials have been considered as a promising alternative to achieve dynamic full-colour tuning towards next-generation electronic display technology. However, the development of electrochromics with wide colour gamut and subtle multicolour tunability still remains challenging due to inflexible energy level structures in intrinsic active materials. Herein, the electrochromic π-conjugated polymers with rich and subtle colour tunability were designed and developed based on a fine adjustment on the energy level structures. The chromatic transition covers almost full-colour gamut, and each colour scheme has a rich variety of categories stemming from versatile hues, chromas and lightnesses. Moreover, the multicolour π-conjugated polymers also demonstrate superior overall electrochromic performance, including fast switching (∼1.0 s), high colouration efficiency (160.4 cm2 C−1@550 nm) and good reversibility (over 90 % retention after 10,000 cycles). As a proof of concept, ultrathin and flexible prototype devices are developed by utilizing the multicolour π-conjugated polymers as electrochromic active layer, exhibiting a wide colour gamut and highly saturated multicolour tunability. The design principles proposed in this work may also be applicable to diverse optoelectronic applications. [ABSTRACT FROM AUTHOR]

[Display omitted] Artificial colloidal motors capable of converting various external energy into mechanical motion, have emerged as attractive photosensitizer (PS) nanocarriers with good deliverability for photodynamic therapy. However, photoactivated 3O 2 -to-1O 2 transformation as the most crucial energy transfer of the photodynamic process itself is still challenging to convert into autonomous transport. Herein, we report on PS-loaded thiophane-containing semiconducting conjugated polymer (SCP)-based polymer colloidal motors with asymmetric geometry for photodynamic-regulated propulsion in the liquid. The asymmetrical presence of the SCP phases within the colloidal motors would lead to significant differences in the 3O 2 -to-1O 2 transformation and 1O 2 release manners between asymmetrical polymer phases, spontaneously creating asymmetrical osmotic pressure gradients across the nanoparticles for powering the self-propelled motion under photodynamic regulation. This photoactivated energy-converting behavior can be also combined with the photothermal conversion of the SCP phases to create two energy gradients exerting diffusiophoretic/thermophoretic force on the colloidal motors for achieving multimode synergistic propulsion. This unique motile feature endows the light-driven PS nanocarriers with good permeability against various physiological barriers in the tumor microenvironment for enhancing antitumor efficacy, showing great potential in phototherapy. [ABSTRACT FROM AUTHOR]

High permittivity materials are required for efficient organic photovoltaic devices, and the addition of the conjugated polymer composite poly(3,4-ethylenedioxythiophen) polystyrene sulfonate (PEDOT:PSS) to dielectric polymers has been shown to significantly heighten their permittivity. The permittivity of PEDOT:PSS at the optical and microwave frequencies has been investigated, but PEDOT:PSS layers are mainly used for low-frequency device applications, where accurate dielectric property measurements are hindered by their high electrical conductivity and the problems arising from the metal-polymer interfaces. Here, we determine the complex relative permittivity ( ε r * = ε r ′ − j ε r ″ ) of PEDOT:PSS layers perpendicular to the layer plane in the 10−2–106 Hz range by combining data from the reactive energy estimations and electrochemical impedance spectroscopy, and discover that: ε r ′ at <1 Hz is ultra-high (∼106) decreasing with frequency to ∼5 at 106 Hz; the experimental data fit the Cole-Cole dielectric relaxation model by considering multiple relaxation mechanisms; PEDOT:PSS polarizes nonlinearly and ε r ′ increases with the intensity of the applied external field; low frequency ε r ′ increases with both thickness and temperature of the layer, opposite trend of temperature-dependence prevails at >103 Hz; the dielectric properties of PEDOT:PSS are highly anisotropic and the in-plane ε r ′ at 1.0 kHz is three orders of magnitude higher than the vertical ε r ′ ; and that the ε r ′ ′ decreases proportional to the reciprocal of frequency (1/f). The latter finding provides an explanation for the ubiquitous pink noise accompanying signals transmitted through organic conductor links. The described methodology can be adopted for investigations on other conjugated polymers. [ABSTRACT FROM AUTHOR]

Organic electrochemical transistors (OECTs) possess low operating voltage and excellent amplification capability and show promising applications in biosensors and flexible electronics. However, the active layers of OECTs are usually dense films, which show limited ion penetration/transport, resulting in limited performances of OECTs. Here, unprecedented high‐performance flexible multifunctional OECTs based on nanoporous (mainly 2–60 nm), high‐specific‐surface‐area (255–281 m2 g−1), and flexible conjugated polymer aerogel films are developed. The nanoporous structures effectively facilitate ion penetration/transport, leading to significantly enhanced transconductance (48.5–53.5 mS) and on/off ratio (6.4 × 104) of the OECTs compared with those of dense devices. The resulting OECT‐based glucose sensors exhibit an ultralow detection limit of 1 pm, approximately two to three orders of magnitude lower than those of the previously reported OECT glucose sensors, and an ultrabroad detection range of 1 pm–5 m. They can detect trace amounts of glucose in sweat, serum, saliva, and urine in real time. Moreover, the OECTs can be used for high‐performance flexible artificial synapses and electrocardiogram monitoring. This work provides a powerful strategy toward highly sensitive biosensors, artificial synapses, and electrophysiological signal monitoring. [ABSTRACT FROM AUTHOR]

Due to their unique semiconducting properties, conjugated porous organic polymers (CPOPs) have garnered significant interest in various photocatalysis applications. In this study, we synthesize three thiazolo[5,4‐d]thiazole (TzTz)‐linked CPOPs with three polyaryl rigid cores of benzene (CPOP1), pyrene (CPOP2), and triazine (CPOP3). We investigated their efficacy in catalyzing visible light‐driven C−N bond formation reactions, including C−N cross‐couplings between aryl bromides and amines and amination reactions from aryl bromides and sodium azides. Among the three, only CPOP2, combined with NiCl2 or Ni(dtbbpy)Cl2, effectively facilitated these transformations. Notably, CPOP2 exhibited photocatalytic activities approximately six times higher than its small molecular counterpart C1 in both reactions. The CPOP catalyst was easily recovered through centrifugal separation and reused for five catalytic cycles with minimal loss of activity. Theoretical calculations revealed that the deliberate structural design of polyaryl moieties could effectively tune the energy gap, which is crucial for the photocatalytic activity in organic reactions. This study, therefore, demonstrates a novel application of TzTz‐linked CPOPs for heterogeneous photocatalytic organic transformations. [ABSTRACT FROM AUTHOR]