Regulation of Charge Transfer Pathway in Ag-ZnIn2S4 Nanowires for Visible Photodynamic Therapy on Candida Albicans Infections.

Photodynamic therapy (PDT) is receiving extensive attention as an antimicrobial strategy that does not cause drug resistance by reactive oxygen species (ROS). Herein, hierarchical Ag-ZnIn2S4 (Ag-ZIS) core-shell nanowires are synthesized by in situ Metal-Organic Framework derived method for efficient PDT of Candida albicans (C. albicans). The core-shell structure enables spatial synergy strategy to regulate the charge transfer pathway under visible light excitation, in which the Ag nanowires are like the highway for the photogenerated electrons. The enhanced charge carrier separation efficiency greatly increased the chances for the generation of ROS. As expected, the optimized Ag-ZIS nanowires exhibit excellent performance for inactivation of C. albicans under visible light irradiation (λ ≥ 420 nm, 15 min), and the effective sterilization concentration is as high as 107CFU mL-1. Moreover, in vivo infection experiments suggested that the PDT effect of Ag-ZIS nanowires on the mouse wound healing is better than that of the clinical Ketoconazole drug. The PDT antifungal mechanism of Ag-ZIS nanowires is also investigated, and superoxide anion is found to be the predominant active species to causes C. albicans damage. This work provides a new perspective for designing novel interface structures to regulate charge transfer to achieve efficient PDT antifungal therapy.

Bamboo-like nitrogen-doped carbon supported chlorine-doped Fe2P as an antibacterial oxygen reduction catalyst.

Bio-inspiration and biomimetics offer guidance for designing and synthesizing advanced catalysts for the oxygen reduction reaction (ORR) in microbial fuel cells (MFCs). Herein, a chlorine-doped Fe2P supported by nitrogen-doped carbon (Cl-Fe2P/NC) catalyst was designed and prepared based on imitating the bamboo structure. The electronegative chlorine captured the electron transfer from Fe2P and transferred it to NC through carbon nanotubes (CNTs). The antibacterial chlorine inhibited the cathode biofilm formation to enhance the ion transport. Cl-Fe2P/NC achieved a half-wave potential of 0.91 V and an onset potential of 0.99 V versus a reversible hydrogen electrode. After 500 h of reaction, the MFCs assembled by the Cl-Fe2P/NC cathode achieved a maximum power density of 1505 mW m-2. This work provides insights into the design of advanced materials through bio-inspiration and biomimicry.

Current perioperative nociception monitoring and potential directions.

Perioperative nociception-antinociception balance is essential for the prevention of adverse postoperative events. Estimating the nociception level helps optimize intraoperative management. In the past two decades, various nociception monitoring devices have been developed for the identification of intraoperative nociception. However, each type of nociception monitoring device has advantages and disadvantages, limiting their clinical application in particular patients and settings. Therefore, this review aimed to summarize the information on nociceptor monitoring in current clinical settings, explore each technique's particularities, and possible future directions to provide a reference for clinicians and researchers.

Unveiling the role of astrocytes in postoperative cognitive dysfunction.

Alzheimer's disease (AD) is the most common neurodegenerative disorder, characterized by progressive cognitive decline and the accumulation of amyloid-beta plaques, tau tangles, and neuroinflammation in the brain. Postoperative cognitive dysfunction (POCD) is a prevalent and debilitating condition characterized by cognitive decline following neuroinflammation and oxidative stress induced by procedures. POCD and AD are two conditions that share similarities in the underlying mechanisms and pathophysiology. Compared to normal aging individuals, individuals with POCD are at a higher risk for developing AD. Emerging evidence suggests that astrocytes, the most abundant glial cells in the central nervous system, play a critical role in the pathogenesis of these conditions. Comprehensive functions of astrocyte in AD has been extensively explored, but very little is known about POCD may experience late-onset AD pathogenesis. Herein, in this context, we mainly explore the multifaceted roles of astrocytes in the context of POCD, highlighting their involvement in neuroinflammation, neurotransmitter regulation, synaptic plasticity and neurotrophic support, and discuss how POCD may augment the onset of AD. Additionally, we discuss potential therapeutic strategies targeting astrocytes to mitigate or prevent POCD, which hold promise for improving the quality of life for patients undergoing surgeries and against AD in the future.

Joule-Heating-Driven Synthesis of a Honeycomb-Like Porous Carbon Nanofiber/High Entropy Alloy Composite as an Ultralightweight Electromagnetic Wave Absorber.

High entropy alloys (HEA) have garnered significant attention in electromagnetic wave (EMW) absorption due to their efficient synergism among multiple components and tunable electronic structures. However, their high density and limited chemical stability hinder their progress as lightweight absorbers. Incorporating HEA with carbon offers a promising solution, but synthesizing stable HEA/carbon composite faces challenges due to the propensity for phase separation during conventional heat treatments. Moreover, EMW absorption mechanisms in HEAs may be different from established empirical models due to their high-entropy effect. This underscores the urgent need to synthesize stable and lightweight HEA/carbon absorbers and uncover their intrinsic absorption mechanisms. Herein, we successfully integrated a quinary FeCoNiCuMn HEA into a honeycomb-like porous carbon nanofiber (HCNF) using electrostatic spinning and the Joule-heating method. Leveraging the inherent lattice distortion effects and honeycomb structure, the HCNF/HEA composite demonstrates outstanding EMW absorption properties at an ultralow filler loading of 2 wt %. It achieves a minimum reflection loss of -65.8 dB and boasts a maximum absorption bandwidth of up to 7.68 GHz. This study not only showcases the effectiveness of combining HCNF with HEA, but also underscores the potential of Joule-heating synthesis for developing lightweight HEA-based absorbers.

Entropy engineering enhances the electromagnetic wave absorption of high-entropy transition metal dichalcogenides/N-doped carbon nanofiber composites.

Entropy engineering strategies provide a broader platform for exploring the behavior of electromagnetic wave (EMW) absorption materials and their absorption mechanisms on the microscopic scale. In this work, a novel entropy engineering strategy was developed to improve the EMW absorption properties of MoS2. A hierarchical N-doped carbon nanofiber/MoS2 (NCNF/MS) composite was synthesized using the electrospinning and hydrothermal methods. Then, the conformational entropy of MoS2 was increased by sequentially integrating elements such as W, Se, and Te. Although MoS2 maintains a single 2H-phase structure throughout the entropy increase process, it triggers a series of complex changes at the microscopic level, including lattice distortion, ingenious electronic structure adjustments, and an increase in defect density. These changes provide more possibilities for the EMW interaction with the absorber, which significantly enhances the dielectric behavior of the composites, including conduction and polarization losses. Owing to the unique hierarchical structure and rich defect structure, the obtained entropy-increased NCNF/MWSST exhibits excellent EMW absorption performance. The minimum reflection loss reaches -60.7 dB, and the maximum effective absorption bandwidth is 6.48 GHz, which is improved by almost 584% and 810% compared to NCNF/MS. This study provides a new way to design efficient and high-performance MoS2-based absorbers and provides valuable insights for exploring the entropy-increasing strategies to optimize the EMW absorption properties.

Preparation of bicyclo[1.1.1]pentane-derived nucleoside analogues.

Nucleoside analogues are prevalent in drug design and call for more diversified structures. Bicyclo[1.1.1]pentane (BCP) structure has recently found wide applications in drug discovery. However, incorporation of BCP fragment into nucleoside analogues is hitherto unknown. Thus, from readily available BCP-containing building blocks, six new compounds, including pyrimidine nucleoside analogues, purine nucleoside analogues, and C-nucleoside analogues were prepared in 1-4 steps, generally with good yields.

Designing flower-like MOFs-derived N-doped carbon nanotubes encapsulated magnetic NiCo composites with multi-heterointerfaces for efficient electromagnetic wave absorption.

In order to acquire exceptional electromagnetic wave absorption properties, the microstructure design and component modification of composites are essential. Metal-organic frameworks (MOFs), due to the unique metal-organic crystalline coordination, tunable morphology, high surface area, and well-defined pores, have been regarded as promising electromagnetic wave absorption materials precursors. However, the inadequate contact abilities between adjacent MOFs nanoparticles endow it with undesirable electromagnetic wave dissipation capacity at a low filler loading, which is a great challenge to break size effect of nanoparticles to achieve efficient absorption. Herein, NiCo-MOFs derived N-doped carbon nanotubes encapsulated with NiCo nanoparticles anchored on flowers-like composites (denoted as NCNT/NiCo/C) were successfully prepared through facile hydrothermal method followed by thermal chemical vapor deposition with melamine-assisted catalyst. By controlling the Ni/Co ratio in precursor, the tunable morphology and microstructure of MOFs are achieved. Most importantly, the derived N-doped carbon nanotubes tightly connect the adjacent nanosheets to construct the special 3D interconnected conductive network, which effectively accelerates the charge transfer and improves the conduction loss. And notably, the NCNT/NiCo/C composite delivers excellent electromagnetic wave absorption performance with minimum reflection loss of -66.1 dB and wide effective absorption bandwidth up to 4.64 GHz when the Ni/Co ratio is 1:1. This work provides a novel method for the preparation of morphology controllable MOFs-derived composites and realizes high-performance electromagnetic wave absorption properties.

Regulating the Charge Migration in CuInSe2 /N-Doped Carbon Nanorod Arrays via Interfacial Engineering for Boosting Photoelectrochemical Water Splitting.

Regulating the charge migration and separation in photoactive materials is a great challenge for developing photoelectrochemical (PEC) applications. Herein, inspired by capacitors, well-defined CuInSe2 /N-doped carbon (CISe/N-C) nanorod arrays are synthesized by Cu/In-metal organic frame-derived method. Like the charge process of capacitor, the N-doped carbon can capture the photogenerated electron of CISe, and the strong interfacial coupling between CISe and N-doped carbon can modulate the charge migration and separation. The optimized the CISe/N-C photoanode achieves a maximum photocurrent of 4.28 mA cm-2 at 1.23 V versus reversible hydrogen electrode (RHE) in neutral electrolyte solution under AM 1.5 G simulated sunlight (100 mW cm-2 ), which is 8.4 times higher than that of the CuInSe2 photoanode (0.51 mA cm-2 ). And a benefit of the strong electronic coupling between CISe and N-doped carbon, the charge transfer rate is increased to 1.3-13 times higher than that of CISe in the range of 0.6-1.1 V versus RHE. The interfacial coupling effects on modulating the carrier transfer dynamics are investigated by Kelvin probe force microscopy analysis and density functional theory calculation. This work provides new insights into bulk phase carrier modulation to improve the performance of photoanode for PEC water splitting.

Advances in Electrochemical Energy Storage over Metallic Bismuth-Based Materials.

Bismuth (Bi) has been prompted many investigations into the development of next-generation energy storage systems on account of its unique physicochemical properties. Although there are still some challenges, the application of metallic Bi-based materials in the field of energy storage still has good prospects. Herein, we systematically review the application and development of metallic Bi-based anode in lithium ion batteries and beyond-lithium ion batteries. The reaction mechanism, modification methodologies and their relationship with electrochemical performance are discussed in detail. Additionally, owing to the unique physicochemical properties of Bi and Bi-based alloys, some innovative investigations of metallic Bi-based materials in alkali metal anode modification and sulfur cathodes are systematically summarized for the first time. Following the obtained insights, the main unsolved challenges and research directions are pointed out on the research trend and potential applications of the Bi-based materials in various energy storage fields in the future.

Multifunctional Mesoporous Hollow Cobalt Sulfide Nanoreactors for Synergistic Chemodynamic/Photodynamic/Photothermal Therapy with Enhanced Efficacy.

The unique tumor microenvironment (TME) characteristic of severe hypoxia, overexpressed intracellular glutathione (GSH), and elevated hydrogen peroxide (H2O2) concentration limit the anticancer effect by monotherapy. In this report, glucose oxidase (GOx)-encapsulated mesoporous hollow Co9S8 nanoreactors are constructed with the coverage of polyphenol diblock polymers containing poly(oligo(ethylene glycol) methacrylate) and dopamine moieties containing methacrylate polymeric block, which are termed as GOx@PCoS. After intravenous injection, tumor accumulation, and cellular uptake, GOx@PCoS deplete GSH by Co3+ ions. GOx inside the nanoreactors produce H2O2 via oxidation of glucose to enhance •OH-based chemodynamic therapy (CDT) through the Fenton-like reaction under the catalysis of Co2+. Moreover, Co3+ ions possess catalase activity to catalyze production of O2 from H2O2 to relieve tumor hypoxia. Upon 808 nm laser irradiation, GOx@PCoS exhibit photothermal and photodynamic effects with a high photothermal conversion efficiency (45.06%) and generation capacity of the toxic superoxide anion (•O2-) for photothermal therapy (PTT) and photodynamic therapy (PDT). The synergetic antitumor effects can be realized by GSH depletion, starvation, and combined CDT, PTT, and PDT with enhanced efficacy. Notably, GOx@PCoS can also be used as a magnetic resonance imaging (MRI) contrast agent to monitor the antitumor performance. Thus, GOx@PCoS show great potentials to effectively modulate TME and perform synergistic multimodal therapy.

Super-stable SnO2/MoS2 enhanced the electrocatalytic hydrogen evolution in acidic environments.

For electrocatalytic hydrogen evolution in acidic environments, the stability of catalysts has always been a significant factor restricting development. Here, we prepared a superstable SnO2/MoS2 coupled nanosheet array on carbon cloth (CC@SnO2/MoS2), exhibiting an overpotential of 166 mV at a current density of 10 mA cm-2. According to the results of various tests and theoretical calculations, it is shown that the establishment of SnO2/MoS2 interface engineering is to accelerate the electron transmission on the heterogeneous interface and S defects on the edge of MoS2, and finally improve the conductivity and catalytic activity of the catalyst. More importantly, the formation of an SnO2 interface layer during in situ transformation improves the stability and hydrophilicity of the material surface. We have proposed a strategy for engineering an interface with fast electron transport and proton adsorption, providing some new ideas for the design of HER catalysts in acid electrolytes.

Oxidation-Resistant MXene-Based Melamine Foam with Ultralow-Percolation Thresholds for Electromagnetic-Infrared Compatible Shielding.

To effectively avoid the drawbacks of conventional metal-based electromagnetic interference (EMI) shielding materials such as high density and susceptibility to corrosion, a multifunctional melamine foam (MF) consisting of MXene/polydimethylsiloxane (PDMS) layers with ultralow percolation thresholds was designed through the electrostatic self-assembly and impregnation strategies. The prepared lightweight foams simultaneously show multifunctional properties including EMI shielding, infrared (IR) stealth, oxidation-resistance, and compression stability. Typically, this multifunctional foam exhibits an excellent EMI shielding efficiency (EMI SE) of 45.2 dB at X-band (8.2-12.4 GHz) with only 1.131 vol % MXene filler. Moreover, the temperature difference between the upper and lower surfaces of the foam can be maintained at 45 °C due to its unique three-dimensional (3D) porous structure and low infrared emissivity. The MF skeleton with MXene/PDMS (MFMXP) displays high hydrophobicity, which remains stable in EMI SE after 60 days of exposure to air. Additionally, it shows outstanding mechanical stability after 100 cycles of compression experiments. The lightweight stealth nanocomposite foams can operate stably in complex environments and show high potential for applications in high-tech fields such as wearable electronics, the military, and semiconductors, etc.

Structure-dependent electrochemical properties of cobalt (II) carbonate hydroxide nanocrystals in supercapacitors.

In this work, we report the structure-dependent electrochemical performance of cobalt carbonate hydroxide (Co2(OH)2CO3) nanocrystals by experimental investigation and theoretical simulation. Different Co2(OH)2CO3 nanostructures including two-dimensional (2D) nanosheets (NSs) and one-dimensional (1D) nanowires (NWs), were synthesized on self-supported carbon cloth substrates by a facile hydrothermal method. Compared to 1D NWs, 2D Co2(OH)2CO3 NSs provided a short ion transfer path, and low electron transfer resistance during the electrochemical reaction. At the current density of 2 mA cm-2, 2D Co2(OH)2CO3 NSs exhibited a higher area capacitance of 2.15F cm-2 and better cycling performance (96.2% retention after 10,000 cycles) than that of 1D NWs (1.15F cm-2 and 90.1% retention). First-principles density functional theory (DFT) calculations revealed that the band gap of the (120) facet in 2D NSs was 0.2 eV, far less than of the (200) facet in 1D NWs (1.04 eV). Electrochemical impedance spectroscopy (EIS) measurements further indicated that the electron transfer and reaction kinetics were more efficient in 2D NSs. This work can provide an important insight in understanding the mechanism of electrochemical energy storage.

Oxygen Vacancy Engineering Synergistic with Surface Hydrophilicity Modification of Hollow Ru Doped CoNi-LDH Nanotube Arrays for Boosting Hydrogen Evolution.

With the development of clean hydrogen energy, the cost effective and high-performance hydrogen evolution reaction (HER) electrocatalysts are urgently required. Herein, a green, facile, and time-efficient Ru doping synergistic with air-plasma treatment strategy is reported to boost the HER performance of CoNi-layered double hydroxide (LDH) nanotube arrays (NTAs) derived from zeolitic imidazolate framework nanorods. The Ru doping and air-plasma treatment not only regulate the oxygen vacancy to optimize the electron structure but also increase the surface roughness to improve the hydrophilicity and hydrogen spillover efficiency. Therefore, the air plasma treated Ru doped CoNi-LDH (P-Ru-CoNi-LDH) nanotube arrays display superior HER performance with an overpotential of 29 mV at a current density of 10 mA cm-2 . Furthermore, by assembling P-Ru-CoNi-LDH as both cathode and anode for two-electrode urea-assisted water electrolysis, a small cell voltage of 1.36 V is needed at 10 mA cm-2 and can last for 100 h without any obvious activity attenuation that showing outstanding durability. In general, the P-Ru-CoNi-LDH can improve the HER performance from intrinsic electronic structure regulation cooperated with extrinsic surface wettability modification. These findings provide an effective intrinsic and extrinsic synergistic effect avenue to develop high performance HER electrocatalysts, which is potential to be applied to other research fields.

Formulating Multiphase Medium Anti-wetting States in an Air-Water-Oil System: Engineering Defects for Interface Chemical Evolutions.

Studies which regulate macroscopic wetting states on determined surfaces in multiphase media are of far-reaching significance but are still in the preliminary stage. Herein, inspired by the wettability subassembly of fish scales, Namib desert beetle shell, and lotus leaf upper side, interfaces in the air-water-oil system are programmed by defect engineering to tailor the anti-wetting evolution from double to triple liquid repellency states. By controlling the visible light irradiation and plasma treatment, surface oxygen vacancies on CuxO@TiO2 nanowires (NWs) can be healed or reconstructed. The original membrane or the membrane after plasma treatment possesses abundant surface oxygen vacancies, and the homogeneous hydrophilic membrane shows only double anti-wetting states in the water-oil system. By the unsaturated visible light irradiation time, the surface oxygen vacancy partially healed, the heterogeneous hydrophilic-hydrophobic components occupied the membrane surface, and the anti-wetting state finally changed from double to triple in the air-water-oil system. After the illumination time reaches saturation, it promotes the healing of all surface oxygen vacancies, and the membrane surface only contains uniform hydrophobic components and only maintains double anti-wetting state in the air-oil system. The mechanism of the triple anti-wetting state on a heterogeneous surface is expounded by establishing a wetting model. The wetting state and the adhesion state of the CuxO@TiO2 NW membrane show regional specificity by controlling the illumination time and region. The underwater oil droplets exhibit the "non-adhesive" and "adhesive" state in a region with unsaturated irradiation time or in an unirradiated region, respectively. Underwater oil droplet manipulation can be accomplished easily based on switchable wettability and adhesion. Current studies reveal that defect engineering can be extended to anti-wetting evolution in the air-water-oil system. Constructing an anti-wetting interface by heterogeneous components provides reference for designing the novel anti-wetting interface.

Interface engineering of a hierarchical ZnxCd1-xS architecture with favorable kinetics for high-performance solar water splitting.

Manipulating the charge carrier transport in photoactive materials is a big challenge toward high efficiency solar water splitting. Herein, we designed a hierarchical ZnxCd1-xS architecture for tuning the interfacial charge transfer kinetics. The in situ growth of ZnxCd1-xS nanoflakes on ZnO backbones provided low interfacial resistance for charge separation. With this special configuration, the optimized Zn0.33Cd0.67S photoanode achieved significantly enhanced performance with a photocurrent density of 10.67 mA cm-2 at 1.23 V versus RHE under AM1.5G solar light irradiation, which is about 14.1 and 2.5 times higher than that of the pristine ZnO and CdS nanoparticle decorated ZnO photoanodes, respectively. After coating a thin SiO2 layer, the photostability of the hierarchical Zn0.33Cd0.67S photoanode is greatly enhanced with 92.33% of the initial value retained under 3600 s continuous light illumination. The prominent PEC activity of the hierarchical ZnxCd1-xS nanorod arrays can be ascribed to an enhanced charge transfer rate aroused by the binder-free interfacial heterojunction, and the improved reaction kinetics at the electrode-electrolyte interface, which is evidenced by electrochemically active surface area measurements and intensity modulated photocurrent spectroscopy analysis. This interfacial heterojunction strategy provides a promising pathway to prepare high performance photoelectrodes.

Ultrathin ZIF-8 wrapping on Au-dotted Ag-nanowires for highly selective SERS-based CO2 gas detection.

Ultrathin ZIF-8 wrapping was constructed on Au-dotted Ag-nanowires to obtain Ag@Au@ZIF-8. A thin film (Ag@Au@ZIF-8 NWs/TF) was constructed to selectively adsorb and enrich CO2 molecules, which solved the problem that SERS signals could not be detected due to the poor affinity of the metal surface and the low concentration of gas molecules.

Solar-Heating Crassula perforata-Structured Superoleophilic CuO@CuS/PDMS Nanowire Arrays on Copper Foam for Fast Remediation of Viscous Crude Oil Spill.

In nature, leaf photosynthesis is the most common solar energy conversion system, which involves light absorption and conversion processes. Most interestingly, the leaves of a green plant are almost lamellar. Herein, inspired by the structure and light conversion capacity of plants, we developed a Crassula perforata-structured CuO@CuS/poly(dimethylsiloxane) (CuO@CuS/PDMS) nanowire arrays (NWAs) on copper foam (CF) with effective light-to-heat conversion to clean up viscous crude oil (∼105 mPa s) by in situ reducing the viscosity of crude oil. The C. perforata-structured CuO@CuS/PDMS core/shell NWAs were grown on copper foam with high density and uniformity, exhibiting excellent light adsorption and photothermal conversion efficiency. When simulated sunlight was irradiated on the structure of the CuO@CuS/PDMS NWAs/CF, abundant heat was generated and in situ reduced the viscosity of crude oil, which prominently increased the oil diffusion coefficient and sped up the oil sorption rate. The oil recovery procedure can realize a continuous clean up with the assistance of a pump device, and the crude oil adsorption capacity can reach up to 15.57 × 105 g/m3 during a 5 min adsorption process. The high-performance photothermal self-heated superoleophilic CuO@CuS/PDMS NWAs/CF has a promise of promoting the practical applications of the sorbents in the clean up of viscous crude oil spills.

Effective photodynamic therapy of polymer hydrogel on tumor cells prepared using methylene blue sensitized mesoporous titania nanocrystal.

A novel hydrogel shell on cancer cells was prepared via in situ photopolymerization of polyethyleneglycol diacrylate (PEGDA) using methylene blue (MB) sensitized mesoporous titania nanocrystal for effective photodynamic therapy (PDT). TiO2 in this system served as an effective photosensitizer and initiator for the formation of hydrogel, also can protect the MB from being degraded into an inactive form. While MB was used as a significant photosensitive additive to improve the photochemistry effects of TiO2 and widen its optical response area to near infrared region (660-900 nm). The PEGDA hydrogel with peritumoral injectability shows competitive advantages, i.e. good biocompatibility and hydrophily, selective and minimally invasive delivery of TiO2@MB, maintaining a high PDT drug concentration for inducing tumor apoptosis, localized and sustainable release under 660 nm laser irradiation for reducing side effect. The hydrogel also could load chemo-therapy drugs, and serve as a versatile platform for multimode antitumor treatment.