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Qianli Ma1*, Wei Wang1*, Paul K Chu2, Shenglin Mei1,2, Kun Ji3, Lei Jin4, Yumei Zhang11Department of Prosthetic Dentistry, School of Stomatology, Fourth Military Medical University, Xi'an, People's Republic of China; 2Department of Physics and Materials Science, City University of Hong Kong, Kowloon, Hong Kong, People's Republic of China; 3Department of Pediatric Dentistry, School of Stomatology, Fourth Military Medical University, Xi'an, People's Republic of China; 4Stomatology Department, Jinling Hospital, School of Medicine, Southern Medical University, Nanjing, People's Republic of China*These authors contributed equally to this workBackground: Titanium (Ti) implants are widely used clinically, but peri-implantitis remains one of the most common and serious complications. Healthy integration between gingival tissue and the implant surface is critical to long-term success in dental implant therapy. The objective of this study was to investigate how different concentrations of immobilized fibroblast growth factor 2 (FGF2) on the titania nanotubular surface influence the response of human gingival fibroblasts (HGFs).Methods: Pure Ti metal was anodized at 20 V to form a vertically organized titanium dioxide nanotube array on which three concentrations of FGF2 (250 ng/mL, 500 ng/mL, or 1000 ng/mL) were immobilized by repeated lyophilization. Surface topography was observed and FGF2 elution was detected using enzyme-linked immunosorbent assay. The bioactivity changes of dissolvable immobilized FGF2 were measured by methyl-thiazolyl-tetrazolium assay. Behavior of HGFs was evaluated using adhesion and methyl-thiazolyl-tetrazolium bromide assays.Results: The FGF2 remained for several days on the modified surface on which HGFs were cultured. Over 90% of the dissolvable immobilized FGF2 had been eluted by Day 9, whereas the FGF2 activity was found to diminish gradually from Day 1 to Day 9. The titania nanotubular surface with an optimal preparing concentration (500 ng/mL) of FGF2 immobilization exhibited improved HGF functions such as cellular attachment, proliferation, and extracellular matrix-related gene expression. Moreover, significant bidirectional as well as concentration- and time-dependent bioactivity was observed.Conclusion: Synergism of the FGF2-impregnated titanium dioxide nanotubular surface revealed good gingival-implant integration, indicating that these materials might have promising applications in dentistry and other biomedical devices.Keywords: dental implants, titanium dioxide nanotube, fibroblast growth factor 2, extracellular matrix, real-time polymerase chain reaction

The development of robust and efficient electrocatalysts for the oxygen evolution reaction (OER) has been the main focus of water electrolysis but remains a great challenge. Here, the synthesis of a highly active and ultra-stable Fe-CoOOH electrocatalyst is reported by steering raw cobalt foam via an in situ solution combustion method assisted by a galvanic replacement reaction and subsequent electrochemical reconstruction of the CoFeO x pre-catalyst. In/ex situ electrochemical analysis and physicochemical characterizations show that the CoFeO x undergoes quick chemical and slow morphological reconstruction to Fe-CoOOH nanosheets. The Fe-CoOOH possesses a semi-crystalline nature with distinct short-range ordering and outstanding OER activity with overpotentials as low as 271 and 291 mV at current densities of 500 and 1,000 mA cm -2 , respectively. The remarkable stability under 1,000 mA cm -2 for at least 700 h is achieved. Theoretical calculations confirm the crucial role of Fe doping in facilitating surface reconstruction, enhancing OER activity, and improving the stability of the Fe-CoOOH. Comparative analysis with other transition metals doping reveals the unique ability of Fe to adsorb onto the CoOOH surface, thereby modulating the electronic density and facilitating faster adsorption of reaction intermediates. This work represents valuable insights into the surface reconstruction and doping processes., (© 2024 Wiley‐VCH GmbH.)

Zinc-ion capacitors (ZICs) have attracted great attention due to a series of advantages. However, the cathode materials are still the bottleneck for high-performance ZICs to be achieved. Therefore, ZIF-8-derived porous carbons are one of the most promising candidates but ZIF-8 nanoparticles with different sizes exhibited various electrochemical performances in ZICs. Herein, a series of monodispersed ZIF-8 nanoparticles are first prepared by a temperature-controlled process to fabricate the corresponding ZIF-8-based porous carbon nanoparticles with pre-designed sizes. The as-prepared materials have been tested as cathode materials in ZICs. Thus, their size effect allowed us to disclose its correlation with other factors such as ion transport/storage and capacitance. The results reveal that the optimal-sized porous carbon particles can effectively shorten the ion transport distance and accelerate the ion diffusion rate, resulting in lower electrical resistance, larger ion diffusion coefficients, and faster electron transport. The presented findings can facilitate the design of new advanced cathode materials paving the way for the development of high-performance cathode materials for ZICs in the future., (© 2024 Wiley‐VCH GmbH.)

The physical killing of bacteria based on surface topography has attracted much attention due to the sustainable and safe prevention of biofilm formation. However, the antibacterial efficiency of biomedical implants derived solely from nanostructures or microstructures is insufficient to combat bacteria against common infections, such as methicillin-resistant Staphylococcus aureus with thick cell walls. Herein, photothermal therapy is carried out in the presence of nanorod arrays to mitigate infection of biomedical implants. Different from traditional photothermal therapy relying on a photosensitizer, the photothermal effect is mediated by light traps rendered by the nanorod arrays, and consequently, the photosensitizer is not needed. Finite element simulations and experiments are performed to elucidate the light-to-thermal conversion mechanism. This photothermal platform, in conjunction with thermosensitive nitric oxide therapy, is applied to treat titanium implant infection. The nanostructure-mediated photothermal effect destroys bacterial cell walls by inhibiting peptidoglycan synthesis and increasing the membrane permeability by affecting fatty acid synthesis. Furthermore, the nanorods synergistically puncture the bacterial membrane easily as demonstrated by experiments and transcriptome analysis. The results provide insights into the development of efficient antibacterial treatment of implants by combining nanostructures and photothermal therapy., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Silicon (Si) is a promising anode material for high-energy-density lithium-ion batteries, but the significant volume change of Si particles during alloying/dealloying with lithium (Li) undermines the mechanical integrity of Si anode, causing electrode fracture, delamination and rapid capacity decay. Herein, a robust triple crosslinked network (TCN) binder with high ionic conductivity and hierarchical stress dissipation is reported for Si anodes, which is prepared by in situ chemical crosslinking polyacrylic acid (PAA) and melamine (MA). The triple interactions of hydrogen bonds, electrostatic interactions, and covalent amide bonds enhance the adhesion of binder to Si and synergistically promote stress dissipation within Si anodes, thus strengthening the dynamic structural stability of Si anodes during cycling. Moreover, the rapid coupling/decoupling of Li + with the TCN binder enables an impressive Li + transference number of 0.63 and high ionic conductivity of 1.2 × 10 -4 S cm -1 . Consequently, the Si-TCN anode delivers specific capacity of 2268 mAh g -1 with a high mass loading of 2 mg cm -2 , high-rate performance of 1673 mAh g -1 at 5 A g -1 , and stable cycling for 250 cycles at 1 A g -1 , thus showing great prospects for high-energy-density Si-based batteries., (© 2024 Wiley‐VCH GmbH.)

A 3D-printed oxygen-vacancy-rich potassium ammonium vanadate/reduced graphene oxide (KNVO v /rGO) microlattice aerogel is designed for the cathode in high-performance K-ion batteries (KIBs). The 3D-printed KNVO v /rGO electrode with periodic submillimeter microchannels and interconnected printed filaments is composed of highly dispersed KNVO v nanobelts, wrinkled graphene nanoflakes, and abundant micropores. The well-defined 3D porous microlattice structure of the rGO backbone not only provides the interconnected conductive 3D network and the required mechanical robustness but also facilitates the penetration of the liquid electrolyte into inner active sites, consequently ensuring a stable electrochemical environment for K-ion intercalation/deintercalation within the KNVO v nanobelts. The 3D-printed KNVO v /rGO microlattice aerogel electrode has a high discharge capacity of 109.3 mAh g -1 with a capacity retention rate of 92.6% after 200 cycles at 50 mA g -1 and maintains a discharge capacity of 75.8 mAh g -1 after 2000 cycles at 500 mA g -1 . The flexible pouch-type KIB battery consisting of the 3D-printed KNVO v /rGO has good mechanical durability and retains a high specific capacity under different forms of deformation such as bending and folding. The results provide valuable insights into the integration of advanced 3D-printed electrode materials into K-ion batteries and the design of flexible and wearable energy storage devices., (© 2024 Wiley‐VCH GmbH.)

Introduction: Emerging evidence suggests long non-coding RNA (lncRNA) H19 is associated with osteoarthritis (OA) pathology. However, how H19 contributes to OA has not been reported. This study aims to investigate the biological function of H19 in OA subchondral bone remodeling and OA progression., Methods: Clinical joint samples and OA animal models induced by medial meniscus destabilization (DMM) surgery were used to verify the causal relationship between osteocyte H19 and OA subchondral bone and cartilage changes. MLO-Y4 osteocyte cells subjected to fluid shear stress were used to verify the mechanism underlying H19-mediated mechano-response. Finally, the antisense oligonucleotide (ASO) against H19 was delivered to mice knee joints by magnetic metal-organic framework (MMOF) nanoparticles in order to develop a site-specific delivery method for targeting osteocyte H19 for OA treatment., Results: Both clinical OA subchondral bone and wildtype mice with DMM-induced OA exhibit aberrant higher subchondral bone mass with more H19 expressing osteocytes. On the contrary, osteocyte-specific deletion of H19 mice is less vulnerable to DMM-induced OA phenotype. In MLO-Y4 cells, H19-mediated osteocyte mechano-response through PI3K/AKT/GSK3 signals activation by EZH2-induced H3K27me3 regulation on PP2A inhibition. Targeted inhibition of H19 (using ASO-loaded MMOF) substantially alleviates subchondral bone remodeling and OA phenotype., Discussion: In summary, our results provide new evidence that the elevated H19 expression in osteocytes may contribute to aberrant subchondral bone remodeling and OA progression. H19 appears to be required for the osteocyte response to mechanical stimulation, and targeting H19 represents a new promising approach for OA treatment., (This article is protected by copyright. All rights reserved.)

Lithium difluoro(oxalate) borate (LiDFOB) contributes actively to cathode-electrolyte interface (CEI) formation, particularly safeguarding high-voltage cathode materials. However, LiNi x Co z Mn y O 2 -based batteries benefit from the LiDFOB and its derived CEI only with appropriate electrolyte design while a comprehensive understanding of the underlying interfacial mechanisms remains limited, which makes the rational design challenging. By performing ab initio calculations, the CEI evolution on the LiNi 0.8 Co 0.1 Mn 0.1 O 2 has been investigated. The findings demonstrate that LiDFOB readily adheres to the cathode via semidissociative configuration, which elevates the Li deintercalation voltage and remains stable in solvent. Electrochemical processes are responsible for the subsequent cleavage of B-F and B-O bonds, while the B-F bond cleavage leading to LiF formation is dominant in the presence of adequate Li + with a substantial Li intercalation energy. Thus, impregnation is established as an effective method to regulate the conversion channel for efficient CEI formation, which not only safeguards the cathode's structure but also counters electrolyte decomposition. Consequently, in comparison to utilizing LiDFOB as an electrolyte additive, employing LiDFOB impregnation in the NCM811/Li cell yields significantly improved cycling stability for over 2000 h.

The depressed directional separation of photogenerated carriers and weak CO 2 adsorption/activation activity are the main factors hampering the development of artificial photosynthesis. Herein, Na ions are embedded in graphitic carbon nitride (g-C 3 N 4 ) to achieve directional migration of the photogenerated electrons to Na sites, while the electron-rich Na sites enhance CO 2 adsorption and activation. Na/g-C 3 N 4 (NaCN) shows improved photocatalytic reduction activity of CO 2 to CO and CH 4 , and under simulated sunlight irradiation, the CO yield of NaCN synthesized by embedding Na at 550°C (NaCN-550) is 371.2 μmol g -1  h -1 , which is 58.9 times more than that of the monomer g-C 3 N 4 . By means of theoretical calculations and experiments including in situ fourier transform infrared spectroscopy, the mechanism is investigated. This strategy which improves carrier separation and reduces the energy barrier at the same time is important to the development of artificial photosynthesis., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

A surface plasmon resonance (SPR) sensor composed of photonic crystal fibers (PCFs) is designed for the detection of low-concentration liquids. The excellent sensing properties are attributed to the sensitivity enhancement at the dispersion turning point (DTP) of the surface plasmon polariton (SPP) modes. The sensor consists of two identical and structurally simple D-shaped PCFs together with a plasmonic thin film coated on the polished surface in direct contact with the analyte. Changes in the refractive index (RI) result in the splitting of the degenerate plasma peaks, thus allowing the monitoring of the analyte concentration variations by measuring the peak separation. In the RI range between 1.328 RIU and 1.33 RIU, the sensor exhibits an ultra-high sensitivity of 129,800 nm/RIU, which is 37.22 times higher than that of the unsensitized single D-shaped structure. Compared to fiber grating sensors operating in the vicinity of the cladding mode DTP, the spliced dual D-shaped PCF still has a predictably high mechanical strength. In addition, the RI detection range of the sensor can be changed by adjusting the slit width. The average sensitivities are 4.38 nm/g·L -1 in the sodium chloride concentration range of 0 g/L to 100 g/L and 20.85 nm/g·L -1 in the hemoglobin concentration range of 0 g/L to 20 g/L. Our results reveal that this SPR sensor based on PCFs has large potential in a variety of applications, especially biochemistry, due to its exceptional sensitivity, structural simplicity, and adjustable detection range.

Cold atmospheric plasma (CAP) is a fledgling therapeutic technique for psoriasis treatment with noninvasiveness, but clinical adoption has been stifled by the insufficient production and delivery of plasma-generated reactive oxygen and nitrogen species (RONS). Herein, patches of air-discharge plasma-activated ice microneedles (PA-IMNs) loaded with multiple RONS are designed for local transdermal delivery to treat psoriasis as an alternative to direct CAP irradiation treatment. By mixing two RONS generated by the air-discharge plasma in the NO x mode and O 3 mode, abundant high-valence RONS are produced and incorporated into PA-IMNs via complex gas-gas and gas-liquid reactions. The PA-IMNs abrogate keratinocyte overproliferation by inducing reactive oxygen species (ROS)-mediated loss of the mitochondrial membrane potential and apoptosis of keratinocytes. The in vivo transdermal treatment confirms that PA-IMNs produce significant anti-inflammatory and therapeutic actions for imiquimod (IMQ)-induced psoriasis-like dermatitis in mice by inhibiting the release of associated inflammatory factors while showing no evident systemic toxicity. Therefore, PA-IMNs have a large potential in transdermal delivery platforms as they overcome the limitations of using CAP directly in the clinical treatment of psoriasis.

Microwave (MW) therapy is an emerging therapy with high efficiency and deep penetration to combat the crisis of bacterial resistance. However, as the energy of MW is too low to induce electron transition, the mechanism of MW catalytic effect remains ambiguous. Herein, a cerium-based metal-organic framework (MOF) is fabricated and used in MW therapy. The MW-catalytic performance of CeTCPP is largely dependent on the ions in the liquid environment, and the electron transition is achieved through a "tribovoltaic effect" between water molecules and CeTCPP. By this way, CeTCPP can generate reactive oxygen species (ROS) in saline under pulsed MW irradiation, showing 99.9995 ± 0.0002% antibacterial ratio against Staphylococcus aureus (S. aureus) upon two cycles of MW irradiation. Bacterial metabolomics further demonstrates that the diffusion of ROS into bacteria led to the bacterial metabolic disorders. The bacteria are finally killed due to "amino acid starvation". In order to improve the applicability of CeTCPP, It is incorporated into alginate-based hydrogel, which maintains good MW catalytic antibacterial efficiency and also good biocompatibility. Therefore, this work provides a comprehensive instruction of using CeTCPP in MW therapy, from mechanism to application. This work also provides new perspectives for the design of antibacterial composite hydrogel., (© 2024 Wiley‐VCH GmbH.)

Atomic engineering of the basal plane active sites in MoS 2 holds great promise to boost the electrocatalytic activity for hydrogen evolution reactions (HER), yet the performance optimization and mechanism exploration are still not satisfactory. Herein, we proposed a dual-plasma engineering strategy to implant Ti and N heteroatoms into the basal plane of MoS 2 supported by Ni 3 S 2 nanorods on nickel foam (MSNF) for efficient electrocatalysis of HER. Owing to the low formation energy of Ti dopants in MoS 2 and the extra charge carriers introduced by N dopants, the optimally codoped samples N1.0@Ti500-MSNF demonstrate significant morphology changes from nanorods to urchin-like nanospheres with the surface active areas increased by seven-fold, as well as enhanced electrical conductivity in comparison with the nondoped counterparts. The HER performance of N1.0@Ti500-MSNF is comparable with the Pt-based catalyst: overpotential of 26 mV at 20 mA cm -2 , Tafel slope of 35.6 mV dec -1 , and long-term stability over 50 h. First-principles calculation reveals that N doping accelerates the dissociation of water molecules while Ti doping activates the adjacent S sites for hydrogen adsorption by lowering the Gibbs free energy, resulting in excellent HER activity. This work thus provides an effective strategy for basal plane engineering of MoS 2 heterostructures toward high-performance HER and sustainable energy supply at reasonable costs.

Two-dimensional (2D) structures composed of atomically thin materials with high carrier mobility have been studied as candidates for future transistors 1-4 . However, owing to the unavailability of suitable high-quality dielectrics, 2D field-effect transistors (FETs) cannot attain the full theoretical potential and advantages despite their superior physical and electrical properties 3,5,6 . Here we demonstrate the fabrication of atomically thin single-crystalline Al 2 O 3 (c-Al 2 O 3 ) as a high-quality top-gate dielectric in 2D FETs. By using intercalative oxidation techniques, a stable, stoichiometric and atomically thin c-Al 2 O 3 layer with a thickness of 1.25 nm is formed on the single-crystalline Al surface at room temperature. Owing to the favourable crystalline structure and well-defined interfaces, the gate leakage current, interface state density and dielectric strength of c-Al 2 O 3 meet the International Roadmap for Devices and Systems requirements 3,5,7 . Through a one-step transfer process consisting of the source, drain, dielectric materials and gate, we achieve top-gate MoS 2 FETs characterized by a steep subthreshold swing of 61 mV dec -1 , high on/off current ratio of 10 8 and very small hysteresis of 10 mV. This technique and material demonstrate the possibility of producing high-quality single-crystalline oxides suitable for integration into fully scalable advanced 2D FETs, including negative capacitance transistors and spin transistors., (© 2024. The Author(s).)

Graphene is a promising candidate for the thermal management of downscaled microelectronic devices owing to its exceptional electrical and thermal properties. Nevertheless, a comprehensive understanding of the intricate electrical and thermal interconversions at a nanoscale, particularly in field-effect transistors with prevalent gate operations, remains elusive. In this study, nanothermometric imaging is used to examine a current-carrying monolayer graphene channel sandwiched between hexagonal boron nitride dielectrics. It is revealed for the first time that beyond the expected Joule heating, the thermoelectric Peltier effect actively plays a significant role in generating hotspots beneath the gated region. With gate-controlled charge redistribution and a shift in the Dirac point position, an unprecedented systematic evolution of thermoelectric hotspots, underscoring their remarkable tenability is demonstrated. This study reveals the field-effect Peltier contribution in a single graphene-material channel of transistors, offering valuable insights into field-effect thermoelectrics and future on-chip energy management., (© 2024 Wiley‐VCH GmbH.)

The quantum conductance (QC) behaviors in synaptic devices with stable and tunable conductance states are essential for high-density storage and brain-like neurocomputing (NC). In this work, inspired by the discontinuous transport of fluid in spider silk, a synaptic device composed of a silicon oxide nanowire network embedded with silicon quantum dots (Si-QDs@SiO x ) is designed. The tunable QC behaviors are achieved in both the SET and RESET processes, and the QC states exhibit stable retention time exceeding 10 4 s in the synaptic device and show stable reproducibility after an interval of two months. The synaptic plasticity, including long-term potentiation/depression and Pavlovian conditioning function, is simulated based on the tunable conductance. The mechanism of stable and tunable QC behaviors is analyzed and clarified by beading effect of spider silk in Si-QDs@SiO x nanowires structure. The digit recognition capability of the device is evaluated by simulation using an artificial neural network consisting of the Si-QDs@SiO x -based synaptic device. These results provide insights into the development of neurocomputing systems with high classification accuracy.

Surface engineering by doping and amorphization is receiving widespread attention from the perspective of the regulation of the electrocatalytic activities of electrocatalysts. However, the effective modulation of active sites on catalysts is still challenging. Herein, a straightforward and efficient method combining hydrothermal treatment with low-temperature plasma processing is presented to synthesize Ni-doped W 18 O 49 nanorod arrays on carbon cloth with abundant oxygen vacancies (CC/WO-Ni- x ). Mild plasma doping with Ni modifies the electronic structure of the W 18 O 49 nanorod arrays, resulting in the formation of an amorphous structure that significantly reduces the electron transfer resistance. Additionally, the coupling with high-valent W 6+ (derived from W 18 O 49 ) leads to the partial preoxidation of doped Ni to form active Ni 3+ species and oxygen vacancies. These features are collectively responsible for the remarkable oxygen evolution reaction (OER) and urea oxidation reaction (UOR) properties of CC/WO-Ni-4, for example, 10 mA cm -2 current density, an overpotential of 265 mV required for the OER under 1.0 M KOH solution. The addition of 500 mM urea to the 1.0 M KOH solution decreases the overpotential required for the same current density from 265 to 93 mV. This study provides insights into the modification of surface structures and presents an effective strategy to optimize the electrocatalytic active sites and enhance the efficiency of multifunctional electrocatalysts.

The discovery of bound states in the continuum (BIC) of optical nanostructures has garnered significant research interest and found widespread application in the field of optics, leading to an attractive approach to achieve high-Q (Quality factor) Fano resonance. Herein, an all-dielectric metasurface consisting of four gallium phosphide (Gap) cylinders on the MgF 2 substrate is designed and analyzed by the finite element method (FEM). By breaking the symmetry of the plane, specifically by moving the two cylinders to one side, it is possible to achieve a transition from the symmetry-protected BIC to quasi-BIC. This transition enables the excitation of sharp dual-band Fano resonance at wavelengths of 1,045.4 nm and 1,139.6 nm, with the maximum Q factors reaching 1.47 × 10 4 and 1.28 × 10 4 , respectively. The multipole decomposition and near-field distributions show that these two QBICs are dominated by the electric quadrupole (EQ) and magnetic quadrupole (MQ). Furthermore, bidirectional optical switching can be accomplished by changing the polarization direction of the incident light. As a result, the maximum sensitivity and figure of merit (FOM) are 488.9 nm/RIU and 2.51 × 10 5 RIU -1 , respectively. The results enrich our knowledge about BIC and reveal a platform for the development of high-performance photonics devices such as optical switches and sensors.

Dual-functional nanomaterial electrodes have the capability to satisfy the requirements for both sweat analysis and the hydrogen evolution reaction (HER), thereby enabling the integration of electrochemical sensing and hydrogen production. In this study, ZIF-67 cubes are synthesized on nickel foam (NF), while TiO 2 is obtained through an annealing process. Subsequently, the ZIF-67@TiO 2 /MoS 2 nanocomposite is fabricated on nickel foam via a hydrothermal method. This composite material exhibits exceptional photocatalytic properties and is also suitable for the detection of glucose in sweat. The glucose detection range spans from 10 nM to 10 mM with a sensitivity of 7.24 μA mM -1  cm - 2 for a signal-to-noise ratio of 3 and a detection limit of 0.43 μM. Moreover, when utilized as a hydrogen evolution electrode, this material demonstrates a current density of 10 mA cm -2 at an overpotential of 118 mV, with a Tafel slope of 73 mV/dec. The synthesis process is both straightforward and economical. This research introduces a novel concept for the design of multifunctional chemical sensors., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

VN usually has poor rate performance and cycle stability. In this work, porous VN nanosheet arrays were prepared on carbon nanofibers embedded with Ti 3 C 2 T x nanosheets by electrospinning and chemical vapor deposition. The 3D network accelerates the transfer of electrons and electrolyte ions, prevents the aggregation of VN and the self-stacking of MXene, and enhances cycle stability. The solid-state flexible device comprising Co 3 O 4 , MXCF@VN, and KOH/PVA exhibits exceptional energy densities of 83.95 W h kg -1 and robust cycling stability (82.8% retention after 20 000 cycles).

Violet phosphorus (VP) has attracted a lot of attention for its unique physicochemical properties and emerging potential in photoelectronic applications. Although VP has a van der Waals (vdW) structure similar to that of other 2D semiconductors, direct synthesis of VP on a substrate is still challenging. Moreover, optoelectronic devices composed of transfer-free VP flakes have not been demonstrated. Herein, a bismuth-assisted vapor phase transport technique is designed to grow uniform single-crystal VP flakes on the SiO 2 /Si substrate directly. The size of the crystalline VP flakes is an order of magnitude larger than that of previous liquid-exfoliated samples. The photodetector fabricated with the VP flakes shows a high responsivity of 12.5 A W -1 and response/recovery time of 3.82/3.03 ms upon exposure to 532 nm light. Furthermore, the photodetector shows a small dark current (<1 pA) that is beneficial to high-sensitivity photodetection. As a result, the detectivity is 1.38 × 10 13 Jones that is comparable with that of the vdW p-n heterojunction detector. The results reveal the great potential of VP in optoelectronic devices as well as the CVT technique for the growth of single-crystal semiconductor thin films., (© 2024 Wiley‐VCH GmbH.)

Enhancing the activation of peroxymonosulfate (PMS) is essential for generating more reactive oxygen species in advanced oxidation process (AOPs). Nevertheless, improving PMS adsorption and expediting interfacial electron transfer to enhance reaction kinetics pose significant challenges. Herein, we construct confined W 18 O 49 nanowires with asymmetric active centers containing Co-Vo-W (Vo: oxygen vacancy). The design incorporates surface-rich Vo and single-atom Co, and the resulting material is employed for PMS activation in water purification. By coupling unsaturated coordinated electrons in Vo with low-valence Co single atoms to construct an the "electron fountainhead", the adsorption and activation of PMS are enhanced. This results in the generation of more active free radicals (SO 4 •- , •OH, •O 2 - ) and non-free radicals ( 1 O 2 ) for the decomposition of micropollutants. Thereinto, the degradation rate of bisphenol A (BPA) by Co-W 18 O 49 is 32.6 times faster that of W 18 O 49 monomer, which is also much higher than those of other transition-metal-doped W 18 O 49 composites. This work is expected to help to elucidate the rational design and efficient PMS activation of catalysts with asymmetric active centers., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)