In this study,sawdust served as a carbon source and urea as a nitrogen source to synthesize carbonsupported,nitrogen-doped TiO_(2)composites via a one-pot solvothermal method.The composites were characterized using FT...In this study,sawdust served as a carbon source and urea as a nitrogen source to synthesize carbonsupported,nitrogen-doped TiO_(2)composites via a one-pot solvothermal method.The composites were characterized using FTIR,powder X-ray diffraction,X-ray photoelectron spectroscopy,ultraviolet-visible diffuse reflectance spectroscopy,thermogravimetry-derivative thermogravimetry,scanning electron microscopy-energy dispersive spectroscopy,and transmission electron microscopy.Results indicated that all synthesized composites exhibit the anatase phase,with those calcined at 800℃ demonstrating enhanced crystallinity.Nitrogen is incorporated into the TiO_(2)lattice,while carbon is predominantly located on the surface.Photodegradation experiments showed that 20 mg of composite N-TiO_(2)/C-800 achieved degradation rates of 93.4% for methylene blue(20 mg·L^(-1),50 mL)and 99.4% for oxytetracycline(20 mg·L^(-1),50 mL)within 30 min.Free radical capture experiments indicated that h+was the primary active species in the photocatalytic degradation process.展开更多
The microbial degradation of aromatic organic pollutants is incomplete due to their metabolic characteristics,which can easily produce certain highly toxic intermediates.Therefore,this article designs a dual template ...The microbial degradation of aromatic organic pollutants is incomplete due to their metabolic characteristics,which can easily produce certain highly toxic intermediates.Therefore,this article designs a dual template molec-ularly imprinted sensor(DTMIP/Fe-Mn@C)for iron manganese metal nanomaterials,prepared Fe-Mn@C com-posite materials by a one pot method were coated on the surface of glassy carbon electrodes and covered with molecularly imprinted membranes through electropolymerization and elution methods,achieving real-time de-tection of specific intermediate products 2-methylbutyric acid(2-MBA)and 3-methylbutyric acid(3-MBA)de-graded by azo dyes.In order to determine the detection sensitivity and intensity range of the sensor,optimization experiments were conducted on various parameters that affect the detection performance,such as the type of func-tional monomer and its composition ratio with the template molecule,detection time window,environmental pH value,etc.Finally,o-Phenylenediamine was determined as the functional monomer,with a molar ratio of 1:1:6 to the template molecules 2-MBA and 3-MBA.Electrochemical testing was conducted in a neutral environment with an incubation time of 5 min and pH=7.The results indicate that the sensor has a relatively wide detection range,high sensitivity,obvious recognition features,and excellent stability for 2-MBA and 3-MBA.This new dual template molecularly imprinted sensor can quickly and accurately determine the safety of highly toxic interme-diates in the degradation process of aromatic organic pollutants,providing a theoretical basis and application potential for trace detection and real-time monitoring.展开更多
While nuclear energy represents a low-carbon and high-efficiency energy source that plays a vital role in the global energy mix,the limitations of spent fuel reprocessing technology pose a major challenge to its susta...While nuclear energy represents a low-carbon and high-efficiency energy source that plays a vital role in the global energy mix,the limitations of spent fuel reprocessing technology pose a major challenge to its sustainable development.The PUREX(plutonium uranium redox extraction)process is currently the dominant nuclear fuel reprocessing technology in the world.However,the key extractant in this process is tributyl phosphate(TBP),which degrades under intense radiation,high temperatures,and strong acidity.This leads to the production of dibutyl phosphate,monobutyl phosphate,and other degradation byproducts,which may reduce the extraction efficiency and trigger third-phase formation and equipment corrosion.This paper systematically reviews the degradation mechanisms of TBP and its diluents,the analytical technique suitable for characterizing degradation products,and the impact of degradation products on the post-treatment process.Additionally,optimization strategies employed for suppressing third-phase formation are discussed.This study offers a theoretical foundation and technical insights in optimizing the PUREX process and ensuring the safe operation of the post-treatment process.展开更多
To overcome the limitations of traditional photocatalysts,such as inefficient separation of charge carriers and poor visible-light absorption,S-scheme g-C_(3)N_(4)/TiO_(2) heterojunction photocatalysts were synthesize...To overcome the limitations of traditional photocatalysts,such as inefficient separation of charge carriers and poor visible-light absorption,S-scheme g-C_(3)N_(4)/TiO_(2) heterojunction photocatalysts were synthesized via a combined method of thermal polymerization,hydrothermal synthesis,and calcination.The crystal structures,morphological features,and optical properties of the composites were systematically characterized,and their photocatalytic performance was evaluated through tetracycline(TC)degradation and hydrogen evolution experiments.Trapping experiments and electron paramagnetic resonance(EPR)measurements were conducted to elucidate the reaction mechanisms.The results demonstrate that the S-scheme heterojunction effectively extends the visible-light absorption range and facilitates the efficient separation of photogenerated electron-hole pairs.Under optimal conditions,the composite achieved a TC degradation rate of 94.5%and a hydrogen evolution rate of 329.1μmol·h^(-1)·g^(-1) after 8 h of irradiation,both values being significantly higher than those of pristine g-C_(3)N_(4) or TiO_(2).Moreover,the S-scheme g-C_(3)N_(4)/TiO_(2) heterojunction retained high photocatalytic activity over five consecutive cycles,confirming its excellent stability.Mechanistic investigations revealed that the S-scheme heterojunction maintained strong redox capacities,with superoxide radicals(·O_(2)^(-)),hydroxyl radicals(·OH),electrons(e-),and holes(h+)serving as the primary active species responsible for TC degradation and H2 production.展开更多
The escalating global issues of water scarcity and pollution emphasize the critical need for the rapid development of efficient and eco-friendly water treatment technologies.Photoelectrocatalytic technology has emerge...The escalating global issues of water scarcity and pollution emphasize the critical need for the rapid development of efficient and eco-friendly water treatment technologies.Photoelectrocatalytic technology has emerged as a promising solution for effectively degrading refractory organic pollutants in water under light conditions.This review delves into the advancements made in the field,focusing on strategies to enhance the generation of active species by modulating the micro-interface of the photoanode.Strategies,such as morphological control,element doping,introduction of surface oxygen vacancies,and construction of heterostructures,significantly improve the separation efficiency of photogenerated charges and the generation of active species,thereby boosting the efficiency of photoelectrocatalytic performance.Furthermore,the review explores the potential applications of photoelectrocatalytic technology in organic pollutant degradation in solutions.It also outlines the current challenges and future development directions.Despite its remarkable laboratory success,practical implementation of photoelectrocatalytic technology encounters obstacles related to stability,cost-effectiveness,and operational efficiency.Future investigations need to focus on optimizing the performance of photoelectrocatalytic materials and exploring strategies for upscaling their application in real water treatment scenarios.展开更多
Synthetic dyes,particularly azo dyes,pose significant environmental and health risks due to their persistence,toxicity,and potential carcinogenicity.Zinc oxide(ZnO)is a promising photocatalyst for wastewater remediati...Synthetic dyes,particularly azo dyes,pose significant environmental and health risks due to their persistence,toxicity,and potential carcinogenicity.Zinc oxide(ZnO)is a promising photocatalyst for wastewater remediation,but its wide bandgap and rapid charge recombination limit its practical efficacy.Furthermore,conventional doping methods often rely on hazardous chemical precursors,undermining the sustainability of the overall approach.This review introduces a novel and sustainable paradigm:the utilization of biomass-derived precursors as green reagents for the in-situ synthesis and simultaneous phosphorus-nitrogen(P-N)co-doping of ZnO nanoparticles.We critically analyze how the intrinsic biochemical composition of biomass,rich in P,N,and other heteroatoms,facilitates this one-pot,eco-friendly functionalization.This integrated strategy merges the performance enhancement offered by advanced co-doping,such as extended visible-light absorption and suppressed charge recombination,with the core principles of green chemistry and circular economy.It offers a dual benefit:creating highly effective photocatalysts for the degradation of persistent pollutants and valorizing abundant agricultural or biological waste streams.Our comprehensive evaluation goes beyond description to critically assess the underlying mechanisms,comparative efficacy,scalability challenges,and future research directions of this emerging field.This review underscores the unique contribution of biomass-mediated synthesis to advancing sustainable nanotechnology for environmental applications.展开更多
Targeted protein degradation(TPD)is an innovative strategy for selectively eliminating pathogenic proteins,enabling precise degradation of once-undruggable targets in cancer therapy.However,current TPD molecules are o...Targeted protein degradation(TPD)is an innovative strategy for selectively eliminating pathogenic proteins,enabling precise degradation of once-undruggable targets in cancer therapy.However,current TPD molecules are often limited by poor tumor targeting and the need for high doses.To overcome these limitations,assembly/disassembly-based TPD systems have been proposed to effectively degrade proteins of interest and enhance therapeutic efficacy.Herein,we summarize the recent advances in such TPD systems and categorize the strategies employed,including nanosphere morphology of assembled TPD systems,nanofiber morphology of assembled TPD systems,carrier-mediated TPD release systems,and stimulus-induced free TPD molecule formation nanosystems.Finally,we outline future directions and identify the remaining challenges in assembly/disassembly-based TPD systems.展开更多
Mycotoxin contamination in food and feed poses a significant global challenge,adversely affecting poultry productivity and compromising both human and animal health.Among mycotoxins,T-2 toxin is of particular concern ...Mycotoxin contamination in food and feed poses a significant global challenge,adversely affecting poultry productivity and compromising both human and animal health.Among mycotoxins,T-2 toxin is of particular concern due to its potent acute toxicity,multi-organ targeting capacity,immunosuppressive effects,and environmental persistence.Biodegradation,particularly enzyme-catalyzed degradation,offers a sustainable and eco-friendly strategy with high specificity for T-2 toxin detoxification.This review comprehensively summarizes key enzymes capable of degrading T-2 toxin,including esterases,glucosyltransferases,glutathione S-transferases,and laccases,with a focus on their respective mechanisms and degradation product profiles.Moreover,the growing demand for enzymes as mycotoxin biodegraders highlights the need for extensive and diverse enzyme resources that can endure harsh reaction conditions.To address this,we propose several methods,including inverse virtual screening,machine learning,and metagenomics,to discover novel enzymes for degradation of mycotoxins including T-2 toxin.Additionally,we highlight the potential of enzyme engineering and genetic optimization strategies to enhance catalytic properties,stability,and production yields of candidate biocatalysts.Overall,this review aims to provide insights and future perspectives to advance the development and practical implementation of enzymatic degradation method for mitigating T-2 toxin contamination.展开更多
The escalating pace of industrialization has significantly intensified water pollution challenges,for instance,the persistent organic pollutants like methyl orange(MO).Conventional remediation techniques,such as adsor...The escalating pace of industrialization has significantly intensified water pollution challenges,for instance,the persistent organic pollutants like methyl orange(MO).Conventional remediation techniques,such as adsorption and biological degradation,are often hampered by low efficiency and the risk of secondary pollution.Photocatalysis emerges as a promising sustainable alternative;however,the benchmark material titanium dioxide(TiO_(2))suffers from its intrinsic limitations,notably its wide bandgap energy(≥3.4 eV)restricting its activity to the region of the ultraviolet light and its rapid recombination of photogenerated charge carriers.To overcome these constraints,this research focused on synthesizing novel TiO_(2)/Sn_(3)O_(4) heterojunction composite photocatalysts via a solvothermal approach.Comprehensive characterization techniques confirmed the successful formation of the composite,which revealed that ultrathin Sn3O4 nanosheets uniformly coated TiO_(2) nanospheres.This unique architecture effectively reduced the overall crystallinity and introduced the beneficial oxygen vacancies.Under visible-light irradiation(λ≥420 nm),the optimized TiO_(2)/Sn3O4 composite exhibited the exceptional photocatalytic performance,which achieved 96%degradation of MO within just 60 minutes.The calculated apparent kinetic rate constant(0.103 min^(-1))was remarkably(5.15 times)higher than that of pristine TiO_(2).ESR experiments identified that hydroxyl radicals(·OH)was the predominant active species driving the degradation.Furthermore,cyclic degradation tests demonstrated its excellent material stability,with the composite retaining 85%of its initial efficiency after four consecutive reuse cycles.This work underscored the synergistic effects within the TiO_(2)/Sn_(3)O_(4) heterojunction,which significantly enhanced the visible-light absorption,charge separation,and photocatalytic activity,which provided the valuable insights for designing efficient,stable catalysts for the advanced environmental remediation applications.展开更多
Pyrethroids are a class of novel broad-spectrum pesticides synthesized to mimic natural pyrethrins.Due to their high efficiency,low toxicity,and safety,pyrethroids have been widely used as alternatives to organophosph...Pyrethroids are a class of novel broad-spectrum pesticides synthesized to mimic natural pyrethrins.Due to their high efficiency,low toxicity,and safety,pyrethroids have been widely used as alternatives to organophosphate and carbamate insecticides in the control of agricultural and sanitary pests.However,with the increasing use of pyrethroid pesticides,the resulting pesticide residues have posed threats to both the environment and human health.Biodegradation is considered one of the most promising methods for the removal of pyrethroids,and significant research has been conducted in this area.This review summarizes recent advances in the biodegradation of pyrethroids,including degradation by single strains,microbial consortia,and enzymes.It provides an in-depth analysis of the biodegradation pathways and catalytic mechanisms involved in the degradation of pyrethroids and outlines enhancement strategies for improving the activity of pyrethroid-degrading enzymes.The review also identifies current challenges in pyrethroid biodegradation and offers perspectives for future research.This review serves as a valuable reference for subsequent studies on pyrethroid biodegradation.展开更多
In this work,we constructed a three-dimensional electrochemical system(3D-ECO),which included the cathode and anode electrode plates,as well as the screening of three-dimensional particle electrodes and parameter opti...In this work,we constructed a three-dimensional electrochemical system(3D-ECO),which included the cathode and anode electrode plates,as well as the screening of three-dimensional particle electrodes and parameter opti-mization,for the degradation of landfill leachate(LL)containing elevated levels of tetracycline(TC),and explored its mechanism of action.Firstly,titanium-based ruthenium-iridium(Ti/RuO_(2)-IrO_(2)),titanium-based ruthenium-iridium-platinum(Ti/Pt-RuO_(2)-IrO_(2)),and titanium-based tin-antimony(Ti/SnO_(2)-Sb_(2)O_(3))were employed as an-odes in the electrocatalytic oxidation system,with titanium and stainless steel plates serving as cathodes,to construct the optimal two-dimensional electrocatalytic oxidation system(2D-ECO)through cross-comparison ex-periments.Subsequently,using granular activated carbon(GAC),coconut shell biochar(CBC),walnut shell carbon(WBC),and bamboo charcoal(BBC)as particle electrodes,a 3D-ECO system was developed.The influence of var-ious operational parameters on treating TC-containing LL was investigated.The optimal operating parameters obtained from the study was:pH=5,current density of 30 mA/cm^(2),particle dosage of 7 g/L,particle size ranging from 1.70 to 2.00 mm,and electrode spacing of 4 cm.Under these conditions,the COD removal rate of 3D-ECO within three hours was 90.25%,the TC removal rate was 72.41%,and the NH_(3)-N removal rate was 39.52%.The removal of TC followed a pseudo-first-order kinetic model.Additionally,degradation mechanisms were elucidated through electron paramagnetic resonance(EPR)spectrometer and Tert-Butanol(TBA)quenching experiments,indicating that the degradation primarily occurred through a non-radical(1O_(2))pathway.This re-search offers a comprehensive analysis of the simultaneous breakdown of intricate LL matrices and TC,enhancing our comprehension of the degradation processes and underlying mechanisms.展开更多
Ocean-degradable polyesters incorporating hydrophilic and rapidly degradable glycolide(GL)units into the polymer chain are the most promising for addressing marine plastic pollution,however,it is challenging to obtain...Ocean-degradable polyesters incorporating hydrophilic and rapidly degradable glycolide(GL)units into the polymer chain are the most promising for addressing marine plastic pollution,however,it is challenging to obtain high-molecular-weight copolymers with narrow molecular weight distributions.Herein,we prepared a novel biodegradable material,poly(butylene succinate-co-glycolide)(PBSGL),through ring-opening copolymerization using glycolide,succinic anhydride,and 1,4-butanediol as raw materials,providing a new solution strategy for marine pollution.GL could be polymerized according to the pre-designed composition by 1H-nuclear magnetic resonance(1H-NMR)and gel permeation chromatography(GPC)results,indicating controlled polymerization with the synthesized PBSGLs having a weight-average molecular weight of up to 12.30×10^(4) g/mol and a narrow molecular weight distribution(1.33–1.65).Differential scanning calorimeter(DSC)and thermogravimetric analysis(TGA)results showed that T_(g) of PBSGLs increased from−32.5°C to−26.5°C with the increase of GL content from 0%to 40%,while T_(m)(>76°C)was much lower than T_(d,5%)(>314°C),which indicated that PBSGLs had good thermal stability and expanded the processing window and application range of the original poly(butylene succinate)(PBS)materials.Under simulated difficult conditions,PBSGL copolyesters could degrade faster with increasing GL content,where PBSGL40 degraded by 22.6%in 12 days,showing good biodegradability.Currently,most biodegradable polyesters with good performance slowly degrade in seawater.In a 30-day artificial seawater degradation test,the amorphous PBSGL40 copolyester showed a about 15-fold(2.33%weight loss)improvement in degradation ability compared to pure PBS,demonstrating rapid seawater degradation capability.展开更多
The effective and environmentally friendly management of oily wastewater,alongside the beneficial conversion of waste biomass,holds paramount importance for environmental conservation,public health,and sustainable soc...The effective and environmentally friendly management of oily wastewater,alongside the beneficial conversion of waste biomass,holds paramount importance for environmental conservation,public health,and sustainable societal progress.In this research,an innovative biomass core-shell bioreactor(CGC@SiO_(2) aerogel) with selective adsorption and degradation properties was developed.The reactor's core is composed of coffee cellulose aerogel,offering a porous framework conducive to microbial colonization while safeguarding microorganisms from adverse external factors.The shell integrates hydrophobic silica enriched with polydimethylsiloxane,which alters the material's hydrophilic properties,enabling it to remain afloat on water for up to 100 days.This superhydrophobic layer maintained a contact angle of 150° even after ten consecutive rubbings.Experimental results indicate that the material performs exceptionally well in oil-water separation,as demonstrated by its success in 9 consecutive oil-water separations.It achieved 99 % selective adsorption,91 % removal,and 46.2 % degradation of a 3 wt.% diesel solution under conditions of 37℃,120 r/min,and pH=7.Additionally,tests assessing environmental tolerance revealed the material's robust adaptability and stability across varying pH levels and temperatures.Compared to traditional hydrophobic and lipophilic materials or free-floating microorganisms,CGC@SiO2 aerogel not only efficiently captures oil pollutants but also degrades them into non-hazardous substances.Combining biodegradation with selective adsorption has shown to be an effective approach for treating oily wastewater,offering significant practical application potential.The low-carbon production of CGC@SiO2aerogel aligns with circular economy principles,underscoring its role in sustainable development.展开更多
As one photovoltaic supernova,perovskite solar cells(PSCs)have exhibited certified power conversion efficiencies exceeding 27%.Yet,the presence of enormous defects,mainly for the dominant iodine vacancy(VI),always ind...As one photovoltaic supernova,perovskite solar cells(PSCs)have exhibited certified power conversion efficiencies exceeding 27%.Yet,the presence of enormous defects,mainly for the dominant iodine vacancy(VI),always induces nonradiative recombination,ion migration,and triggers autocatalytic iodine oxidation into volatile I_(2) and charge-localization-mediated metallic Pb0clusters,which accelerate device failure and therefore hamper commercialization.However,popularly reported strategies that simultaneously enable vacancy passivation and iodine scavenging remain insufficient,highlighting the need for new additives.Herein,we employ 4-cyanophenylhydrazine hydrochloride(CPHCl)as an iodine-related synergistic redox-coordination stabilizer to address intrinsic instability and interface chemistry issues.After systematically characterizations,we demonstrate that CPHCl not only specifically eliminates I_(2) intermediates by leveraging the redox-active hydrazine group(NH–NH_(2))(I_(2)+NH–NH_(2)→2HI+N=NH),but also passivates Pb^(2+)/FA^(+) related defects viaπ-backdonation and hydrogen bonding by the electron-donating cyano(C≡N)group,synergistically modulating the crystallization kinetics and improving the final quality of the perovskite film.As a result,vacancy-mediated I-ion migration and degradation are significantly relieved,enabling an enhanced efficiency of 25.56%for the p-i-n inverted PSC with exceptional operational stability.This work provides a deep insight into screening perovskite stabilizers for advancing toward commercial longevity.展开更多
Molecular glues(MGs), a class of small-molecule degraders, exhibit drug-like properties that generally conform to Lipinski's rule of five, while uniquely mediating the stabilization or induction of protein-protein...Molecular glues(MGs), a class of small-molecule degraders, exhibit drug-like properties that generally conform to Lipinski's rule of five, while uniquely mediating the stabilization or induction of protein-protein interactions. By altering the surface properties of either target proteins or E3 ligases, MGs promote the formation of a ternary complex comprising the MG, an E3 ligase, and a target protein. This interaction facilitates the polyubiquitination and subsequent degradation of the target protein via the ubiquitin-proteasome system.Owing to its distinctive mechanism of action and broad therapeutic potential, MG is offering novel approaches to disease treatment. This review summarizes recent advances in MGs targeting NEK7, WEE1, CDK2, GSPT1 and VAV1, emphasizing the rational design, benefits,and potential limitations, highlighting rational design principles, advantages, and current limitations including challenges in achieving selectivity and rational design that provide critical insights for enhancing MG efficacy. These developments are crucial for advancing the application and optimization of molecular glues targeting NEK7, WEE1, CDK2, GSPT1and VAV1.展开更多
Antibiotics are emerging pollutants that pose significant risks to environmental and human health.Periodate(PI)-based advanced oxidation processes have shown promise for their effective degradation.In this study,we sy...Antibiotics are emerging pollutants that pose significant risks to environmental and human health.Periodate(PI)-based advanced oxidation processes have shown promise for their effective degradation.In this study,we systematically investigate the structure-activity relationship of four representative Fe-based metal-organic frameworks(Fe-MOFs)-MIL-101(Fe),MIL-88B(Fe),MIL-88A(Fe),and MIL-53(Fe)-as PI activators for tetracycline(TC)degradation.Among them,MIL-101(Fe)exhibited the highest catalytic performance,owing to its unique Fe3O-OH nodes and mesoporous architecture.The MIL-101(Fe)/PI system achieved 93.3%TC degradation and 55.9%mineralization rate within 60 min.Mechanistic studies combining scavenger quenching,sulfoxide probe transformation,X-ray photoelectron spectroscopy,and X-ray absorption fine structure confirmed the generation of multiple reactive oxygen species,and high-valent Fe(IV)]O and O_(2)^(·-)played major roles in the tetracycline degradation process.Density functional theory calculations further revealed that MIL-101(Fe)and MIL-88B(Fe)effectively interact with PI to form Fe(Ⅲ)-superoxide(Fe(Ⅲ)-O-O^(·-)),a key intermediate in Fe(IV)]O generation.In contrast,the adsorption energy of MIL-53(Fe)and MIL-88A(Fe)was relatively weak,with fewer binding sites,resulting in poor performance.The synergy between Fe(Ⅲ)-O-O^(·-)formation and the pore accessibility of MIL-101(Fe)accounted for its superior catalytic efficiency.This work not only clarifies the structural factors governing PI activation in Fe-MOFs,but also proposes a mechanistically informed strategy for designing high-performance catalysts for antibiotic degradation.展开更多
Oxidative magnetization has attracted great attention as an efficient strategy for modulating physiochemical properties of magnetic biochar.In this paper,a K_(2)FeO_(4)-involving hydrothermal oxidative magnetization w...Oxidative magnetization has attracted great attention as an efficient strategy for modulating physiochemical properties of magnetic biochar.In this paper,a K_(2)FeO_(4)-involving hydrothermal oxidative magnetization was explored to regulate multiple micro-structures for manufacture magnetic hydrochar(MHC)for Fenton-like degradation of tetracycline in aqueous solution.Diverse shapes of Fe_(3)O_(4) and nano zero-valent iron(nZVI)were doped with abundant oxygen containing groups and persistent free radicals(PFRs).Multiple catalysis sites including iron species,PFRs,oxygen containing groups,and graphite defects contributed to accelerate the Fenton-like degradation with synergistic effect.Notably,MHC achieved a tetracycline removal rate of 99% within 60 min at 50 mg/L,with a total organic carbon(TOC)removal rate of 35%.Furthermore,after four cycles of reuse,the degradation efficiency slightly decreased to 93%.This study highlights the potential of magnetic hydrochar with multiple catalytic sites in the effective and sustainable degradation of pollutants.展开更多
Hydrogel zinc ion batteries(HZIBs)represent a cutting-edge advancement in energy storage systems,leveraging the exceptional properties of hydrogels,including superior mechanical flexibility and robust structural stabi...Hydrogel zinc ion batteries(HZIBs)represent a cutting-edge advancement in energy storage systems,leveraging the exceptional properties of hydrogels,including superior mechanical flexibility and robust structural stability.Despite their promising attributes,HZIBs face persistent challenges that hinder their practical deployment,notably performance degradation during long-term cycling.In this review,we provide a comprehensive explanation of the fundamental structure and working principles of HZIBs,analyzing the roles of each component.We then systematically explore these degradation mechanisms and comprehensively summarize the key influencing factors,including zinc dendrite formation,hydrogel matrix degradation,electrolyte depletion,and interfacial instability.The role of environmental and operational factors,such as temperature fluctuations and humidity variations,in exacerbating these degradation processes is also highlighted.Recent material engineering strategies to mitigate these issues are summarized:1)the development of structurally reinforced hydrogel electrolytes;2)the use of functional additives for ion transport regulation;and 3)interfacial engineering for uniform zinc deposition.Moreover,emerging fabrication techniques,such as nanoscale structural design and additive manufacturing,are discussed for their potential to optimize the mechanical robustness and electrochemical performance of HZIBs.This review integrates fundamental insights with advanced engineering approaches to provide practical guidance for the scalable development of high performance HZIBs for flexible and wearable applications.展开更多
The excessive use of pesticides has exacerbated environmental pollution due to herbicide residues,while their persistent toxicity poses serious challenges to global ecological security.A magnetically recyclable CoFe_(...The excessive use of pesticides has exacerbated environmental pollution due to herbicide residues,while their persistent toxicity poses serious challenges to global ecological security.A magnetically recyclable CoFe_(2)O_(4)/BiOBr S-scheme heterojunctions was prepared by microwave-assisted co-precipitation method for photocatalytic degradation of Diuron(DUR) in water.The formation of S-scheme heterojunction enhances electron transfer and charge separation,which was demonstrated by free radical trapping,electrochemical experiments,and DFT calculations.The magnetic CoFe_(2)O_(4)/BiOBr catalysts can achieve 99.9 %removal of diuron in 50 min under visible light irradiation.Furthermore,the system maintains stable performance across a broad p H range(3-9),enabling adaptation to diverse water environments,effective elimination of multiple pollutants,and strong resistance to ionic interference.Using magnetic recovery,CoFe_(2)O_(4)/BiOBr exhibits a high removal rate of 99 % and a markedly low ion leaching rate(<20 μg/L) after six cycles photocatalytic process,confirming its excellent stability and durability.According to HPLCQTOF-MS and DFT calculation,the main ways of DUR degradation include dechlorinated hydroxylation,dealkylation and hydroxylation of aromatic ring and side chain.Toxicity analysis showed that the toxicity of the intermediates generated during degradation was generally lower than that of DUR.The magnetic CoFe_(2)O_(4)/BiOBr S-scheme heterojunction developed in this study exhibits excellent photocatalytic performance,high applicability,good stability,and durability,providing an effective magnetic for the removal of refractory pollutants.展开更多
Rui Chena,b,Tangbing Cui a,b,∗a School of Biology and Biological Engineering,South China University of Technology,Guangzhou 510006,China b Guangdong Key Laboratory of Fermentation and Enzyme Engineering,South China Un...Rui Chena,b,Tangbing Cui a,b,∗a School of Biology and Biological Engineering,South China University of Technology,Guangzhou 510006,China b Guangdong Key Laboratory of Fermentation and Enzyme Engineering,South China University of Technology,Guangzhou 510006,China The authors regret that the published version of this article contained several errors and omissions,which are described and corrected below.1.Figs.3 and 4(figure order and legends).In the published article,Figs.3 and 4 were inadvertently published in reversed order.The figures should be swapped so that the figure content matches its caption.The correct figures and their legends are provided on the following page.2.Title correction.The compound name in the published title was incorrectly typeset as“benzo[a]pyrene”The correct spelling is“benzo[a]pyrene.”3.Text corrections in Section 2.4.Several typographical errors occurred in Section 2.4(“Up-regulation of acetoin,lactate,and kanosamine biosynthesis under sodium gluconate treatment”).展开更多
文摘In this study,sawdust served as a carbon source and urea as a nitrogen source to synthesize carbonsupported,nitrogen-doped TiO_(2)composites via a one-pot solvothermal method.The composites were characterized using FTIR,powder X-ray diffraction,X-ray photoelectron spectroscopy,ultraviolet-visible diffuse reflectance spectroscopy,thermogravimetry-derivative thermogravimetry,scanning electron microscopy-energy dispersive spectroscopy,and transmission electron microscopy.Results indicated that all synthesized composites exhibit the anatase phase,with those calcined at 800℃ demonstrating enhanced crystallinity.Nitrogen is incorporated into the TiO_(2)lattice,while carbon is predominantly located on the surface.Photodegradation experiments showed that 20 mg of composite N-TiO_(2)/C-800 achieved degradation rates of 93.4% for methylene blue(20 mg·L^(-1),50 mL)and 99.4% for oxytetracycline(20 mg·L^(-1),50 mL)within 30 min.Free radical capture experiments indicated that h+was the primary active species in the photocatalytic degradation process.
基金supported by the Bingtuan Industrial Technology Research Institute,Bingtuan New materials Research Institute innovation platform project,Research initiation project of Shihezi University(No.RCZK202330)the Science and Technology Program-Regional Innovation Guidance Program(No.2023ZD080)Tianchi Talent Project(No.CZ002735).
文摘The microbial degradation of aromatic organic pollutants is incomplete due to their metabolic characteristics,which can easily produce certain highly toxic intermediates.Therefore,this article designs a dual template molec-ularly imprinted sensor(DTMIP/Fe-Mn@C)for iron manganese metal nanomaterials,prepared Fe-Mn@C com-posite materials by a one pot method were coated on the surface of glassy carbon electrodes and covered with molecularly imprinted membranes through electropolymerization and elution methods,achieving real-time de-tection of specific intermediate products 2-methylbutyric acid(2-MBA)and 3-methylbutyric acid(3-MBA)de-graded by azo dyes.In order to determine the detection sensitivity and intensity range of the sensor,optimization experiments were conducted on various parameters that affect the detection performance,such as the type of func-tional monomer and its composition ratio with the template molecule,detection time window,environmental pH value,etc.Finally,o-Phenylenediamine was determined as the functional monomer,with a molar ratio of 1:1:6 to the template molecules 2-MBA and 3-MBA.Electrochemical testing was conducted in a neutral environment with an incubation time of 5 min and pH=7.The results indicate that the sensor has a relatively wide detection range,high sensitivity,obvious recognition features,and excellent stability for 2-MBA and 3-MBA.This new dual template molecularly imprinted sensor can quickly and accurately determine the safety of highly toxic interme-diates in the degradation process of aromatic organic pollutants,providing a theoretical basis and application potential for trace detection and real-time monitoring.
基金supported by the Youth Talent Project of China Nuclear Power Engineering Co.,Ltd.(KY24045).
文摘While nuclear energy represents a low-carbon and high-efficiency energy source that plays a vital role in the global energy mix,the limitations of spent fuel reprocessing technology pose a major challenge to its sustainable development.The PUREX(plutonium uranium redox extraction)process is currently the dominant nuclear fuel reprocessing technology in the world.However,the key extractant in this process is tributyl phosphate(TBP),which degrades under intense radiation,high temperatures,and strong acidity.This leads to the production of dibutyl phosphate,monobutyl phosphate,and other degradation byproducts,which may reduce the extraction efficiency and trigger third-phase formation and equipment corrosion.This paper systematically reviews the degradation mechanisms of TBP and its diluents,the analytical technique suitable for characterizing degradation products,and the impact of degradation products on the post-treatment process.Additionally,optimization strategies employed for suppressing third-phase formation are discussed.This study offers a theoretical foundation and technical insights in optimizing the PUREX process and ensuring the safe operation of the post-treatment process.
文摘To overcome the limitations of traditional photocatalysts,such as inefficient separation of charge carriers and poor visible-light absorption,S-scheme g-C_(3)N_(4)/TiO_(2) heterojunction photocatalysts were synthesized via a combined method of thermal polymerization,hydrothermal synthesis,and calcination.The crystal structures,morphological features,and optical properties of the composites were systematically characterized,and their photocatalytic performance was evaluated through tetracycline(TC)degradation and hydrogen evolution experiments.Trapping experiments and electron paramagnetic resonance(EPR)measurements were conducted to elucidate the reaction mechanisms.The results demonstrate that the S-scheme heterojunction effectively extends the visible-light absorption range and facilitates the efficient separation of photogenerated electron-hole pairs.Under optimal conditions,the composite achieved a TC degradation rate of 94.5%and a hydrogen evolution rate of 329.1μmol·h^(-1)·g^(-1) after 8 h of irradiation,both values being significantly higher than those of pristine g-C_(3)N_(4) or TiO_(2).Moreover,the S-scheme g-C_(3)N_(4)/TiO_(2) heterojunction retained high photocatalytic activity over five consecutive cycles,confirming its excellent stability.Mechanistic investigations revealed that the S-scheme heterojunction maintained strong redox capacities,with superoxide radicals(·O_(2)^(-)),hydroxyl radicals(·OH),electrons(e-),and holes(h+)serving as the primary active species responsible for TC degradation and H2 production.
基金financially supported by the National Natural Science Foundation of China (No.52100076)the Fundamental Research Funds for the Central Universities (No.2023MS064)。
文摘The escalating global issues of water scarcity and pollution emphasize the critical need for the rapid development of efficient and eco-friendly water treatment technologies.Photoelectrocatalytic technology has emerged as a promising solution for effectively degrading refractory organic pollutants in water under light conditions.This review delves into the advancements made in the field,focusing on strategies to enhance the generation of active species by modulating the micro-interface of the photoanode.Strategies,such as morphological control,element doping,introduction of surface oxygen vacancies,and construction of heterostructures,significantly improve the separation efficiency of photogenerated charges and the generation of active species,thereby boosting the efficiency of photoelectrocatalytic performance.Furthermore,the review explores the potential applications of photoelectrocatalytic technology in organic pollutant degradation in solutions.It also outlines the current challenges and future development directions.Despite its remarkable laboratory success,practical implementation of photoelectrocatalytic technology encounters obstacles related to stability,cost-effectiveness,and operational efficiency.Future investigations need to focus on optimizing the performance of photoelectrocatalytic materials and exploring strategies for upscaling their application in real water treatment scenarios.
文摘Synthetic dyes,particularly azo dyes,pose significant environmental and health risks due to their persistence,toxicity,and potential carcinogenicity.Zinc oxide(ZnO)is a promising photocatalyst for wastewater remediation,but its wide bandgap and rapid charge recombination limit its practical efficacy.Furthermore,conventional doping methods often rely on hazardous chemical precursors,undermining the sustainability of the overall approach.This review introduces a novel and sustainable paradigm:the utilization of biomass-derived precursors as green reagents for the in-situ synthesis and simultaneous phosphorus-nitrogen(P-N)co-doping of ZnO nanoparticles.We critically analyze how the intrinsic biochemical composition of biomass,rich in P,N,and other heteroatoms,facilitates this one-pot,eco-friendly functionalization.This integrated strategy merges the performance enhancement offered by advanced co-doping,such as extended visible-light absorption and suppressed charge recombination,with the core principles of green chemistry and circular economy.It offers a dual benefit:creating highly effective photocatalysts for the degradation of persistent pollutants and valorizing abundant agricultural or biological waste streams.Our comprehensive evaluation goes beyond description to critically assess the underlying mechanisms,comparative efficacy,scalability challenges,and future research directions of this emerging field.This review underscores the unique contribution of biomass-mediated synthesis to advancing sustainable nanotechnology for environmental applications.
基金supported by National Natural Science Foundation of China(Grant 22407024)the Star-up Research Fund of Southeast University(RF1028624094)(X.W.)+7 种基金the China Postdoctoral Science Foundation(Grant 2025M772911)Natural Science Foundation of Jiangsu Province(Grants BK20251303)(X.L.)Postdoctoral Fellowship Program of CPSF(Grant GZC20251914)(X.L.)Jiangsu Funding Program for Excellent Postdoctoral Talent(Grant 2025ZB052)(X.L.)National Natural Science Foundation of China(Grant 22234002)(G.L.)National Key Research and Development Program of China(Grant 2023YFF0724100)(G.L.)Natural Science Foundation of Jiangsu Province(Grant BK20232007)(G.L.)Jiangsu ShuangChuang Team(Grant JSSCTD202409)(G.L.and X.W.).
文摘Targeted protein degradation(TPD)is an innovative strategy for selectively eliminating pathogenic proteins,enabling precise degradation of once-undruggable targets in cancer therapy.However,current TPD molecules are often limited by poor tumor targeting and the need for high doses.To overcome these limitations,assembly/disassembly-based TPD systems have been proposed to effectively degrade proteins of interest and enhance therapeutic efficacy.Herein,we summarize the recent advances in such TPD systems and categorize the strategies employed,including nanosphere morphology of assembled TPD systems,nanofiber morphology of assembled TPD systems,carrier-mediated TPD release systems,and stimulus-induced free TPD molecule formation nanosystems.Finally,we outline future directions and identify the remaining challenges in assembly/disassembly-based TPD systems.
基金supported by the Hubei Province Regional Science and Technology Innovation Plan Project(2025EHA016).
文摘Mycotoxin contamination in food and feed poses a significant global challenge,adversely affecting poultry productivity and compromising both human and animal health.Among mycotoxins,T-2 toxin is of particular concern due to its potent acute toxicity,multi-organ targeting capacity,immunosuppressive effects,and environmental persistence.Biodegradation,particularly enzyme-catalyzed degradation,offers a sustainable and eco-friendly strategy with high specificity for T-2 toxin detoxification.This review comprehensively summarizes key enzymes capable of degrading T-2 toxin,including esterases,glucosyltransferases,glutathione S-transferases,and laccases,with a focus on their respective mechanisms and degradation product profiles.Moreover,the growing demand for enzymes as mycotoxin biodegraders highlights the need for extensive and diverse enzyme resources that can endure harsh reaction conditions.To address this,we propose several methods,including inverse virtual screening,machine learning,and metagenomics,to discover novel enzymes for degradation of mycotoxins including T-2 toxin.Additionally,we highlight the potential of enzyme engineering and genetic optimization strategies to enhance catalytic properties,stability,and production yields of candidate biocatalysts.Overall,this review aims to provide insights and future perspectives to advance the development and practical implementation of enzymatic degradation method for mitigating T-2 toxin contamination.
文摘The escalating pace of industrialization has significantly intensified water pollution challenges,for instance,the persistent organic pollutants like methyl orange(MO).Conventional remediation techniques,such as adsorption and biological degradation,are often hampered by low efficiency and the risk of secondary pollution.Photocatalysis emerges as a promising sustainable alternative;however,the benchmark material titanium dioxide(TiO_(2))suffers from its intrinsic limitations,notably its wide bandgap energy(≥3.4 eV)restricting its activity to the region of the ultraviolet light and its rapid recombination of photogenerated charge carriers.To overcome these constraints,this research focused on synthesizing novel TiO_(2)/Sn_(3)O_(4) heterojunction composite photocatalysts via a solvothermal approach.Comprehensive characterization techniques confirmed the successful formation of the composite,which revealed that ultrathin Sn3O4 nanosheets uniformly coated TiO_(2) nanospheres.This unique architecture effectively reduced the overall crystallinity and introduced the beneficial oxygen vacancies.Under visible-light irradiation(λ≥420 nm),the optimized TiO_(2)/Sn3O4 composite exhibited the exceptional photocatalytic performance,which achieved 96%degradation of MO within just 60 minutes.The calculated apparent kinetic rate constant(0.103 min^(-1))was remarkably(5.15 times)higher than that of pristine TiO_(2).ESR experiments identified that hydroxyl radicals(·OH)was the predominant active species driving the degradation.Furthermore,cyclic degradation tests demonstrated its excellent material stability,with the composite retaining 85%of its initial efficiency after four consecutive reuse cycles.This work underscored the synergistic effects within the TiO_(2)/Sn_(3)O_(4) heterojunction,which significantly enhanced the visible-light absorption,charge separation,and photocatalytic activity,which provided the valuable insights for designing efficient,stable catalysts for the advanced environmental remediation applications.
基金supported by grants from the National Natural Science Foundation of China(No.42207148)the Science and Technology Plan Project of Quanzhou,China(Nos.2025QZNS002 and 2022N030)+2 种基金the Natural Science Foundation of Fujian Province,China(No.2022J01573)the Educational Research Project for Young and Middle-Aged Teachers in Fujian Province,China(No.JAT210042)the Open Project Fund of Key Laboratory of Marine Biological Resources,Ministry of Natural Resources of China(Nos.HY202201 and HY202202)。
文摘Pyrethroids are a class of novel broad-spectrum pesticides synthesized to mimic natural pyrethrins.Due to their high efficiency,low toxicity,and safety,pyrethroids have been widely used as alternatives to organophosphate and carbamate insecticides in the control of agricultural and sanitary pests.However,with the increasing use of pyrethroid pesticides,the resulting pesticide residues have posed threats to both the environment and human health.Biodegradation is considered one of the most promising methods for the removal of pyrethroids,and significant research has been conducted in this area.This review summarizes recent advances in the biodegradation of pyrethroids,including degradation by single strains,microbial consortia,and enzymes.It provides an in-depth analysis of the biodegradation pathways and catalytic mechanisms involved in the degradation of pyrethroids and outlines enhancement strategies for improving the activity of pyrethroid-degrading enzymes.The review also identifies current challenges in pyrethroid biodegradation and offers perspectives for future research.This review serves as a valuable reference for subsequent studies on pyrethroid biodegradation.
基金supported by the National Natural Science Foundation of China(Nos.42477406 and 51878617)the Horizontal Scientific Research Project(No.KYY-HX-20220803)the Engineering Research Center of Ministry of Education for Renewable Energy Infrastructure Construction Technology.
文摘In this work,we constructed a three-dimensional electrochemical system(3D-ECO),which included the cathode and anode electrode plates,as well as the screening of three-dimensional particle electrodes and parameter opti-mization,for the degradation of landfill leachate(LL)containing elevated levels of tetracycline(TC),and explored its mechanism of action.Firstly,titanium-based ruthenium-iridium(Ti/RuO_(2)-IrO_(2)),titanium-based ruthenium-iridium-platinum(Ti/Pt-RuO_(2)-IrO_(2)),and titanium-based tin-antimony(Ti/SnO_(2)-Sb_(2)O_(3))were employed as an-odes in the electrocatalytic oxidation system,with titanium and stainless steel plates serving as cathodes,to construct the optimal two-dimensional electrocatalytic oxidation system(2D-ECO)through cross-comparison ex-periments.Subsequently,using granular activated carbon(GAC),coconut shell biochar(CBC),walnut shell carbon(WBC),and bamboo charcoal(BBC)as particle electrodes,a 3D-ECO system was developed.The influence of var-ious operational parameters on treating TC-containing LL was investigated.The optimal operating parameters obtained from the study was:pH=5,current density of 30 mA/cm^(2),particle dosage of 7 g/L,particle size ranging from 1.70 to 2.00 mm,and electrode spacing of 4 cm.Under these conditions,the COD removal rate of 3D-ECO within three hours was 90.25%,the TC removal rate was 72.41%,and the NH_(3)-N removal rate was 39.52%.The removal of TC followed a pseudo-first-order kinetic model.Additionally,degradation mechanisms were elucidated through electron paramagnetic resonance(EPR)spectrometer and Tert-Butanol(TBA)quenching experiments,indicating that the degradation primarily occurred through a non-radical(1O_(2))pathway.This re-search offers a comprehensive analysis of the simultaneous breakdown of intricate LL matrices and TC,enhancing our comprehension of the degradation processes and underlying mechanisms.
基金financially supported by the National Natural Science Foundation of China (No. 52203012)Shanghai Rising-Star Program (No. 23QC1400900).
文摘Ocean-degradable polyesters incorporating hydrophilic and rapidly degradable glycolide(GL)units into the polymer chain are the most promising for addressing marine plastic pollution,however,it is challenging to obtain high-molecular-weight copolymers with narrow molecular weight distributions.Herein,we prepared a novel biodegradable material,poly(butylene succinate-co-glycolide)(PBSGL),through ring-opening copolymerization using glycolide,succinic anhydride,and 1,4-butanediol as raw materials,providing a new solution strategy for marine pollution.GL could be polymerized according to the pre-designed composition by 1H-nuclear magnetic resonance(1H-NMR)and gel permeation chromatography(GPC)results,indicating controlled polymerization with the synthesized PBSGLs having a weight-average molecular weight of up to 12.30×10^(4) g/mol and a narrow molecular weight distribution(1.33–1.65).Differential scanning calorimeter(DSC)and thermogravimetric analysis(TGA)results showed that T_(g) of PBSGLs increased from−32.5°C to−26.5°C with the increase of GL content from 0%to 40%,while T_(m)(>76°C)was much lower than T_(d,5%)(>314°C),which indicated that PBSGLs had good thermal stability and expanded the processing window and application range of the original poly(butylene succinate)(PBS)materials.Under simulated difficult conditions,PBSGL copolyesters could degrade faster with increasing GL content,where PBSGL40 degraded by 22.6%in 12 days,showing good biodegradability.Currently,most biodegradable polyesters with good performance slowly degrade in seawater.In a 30-day artificial seawater degradation test,the amorphous PBSGL40 copolyester showed a about 15-fold(2.33%weight loss)improvement in degradation ability compared to pure PBS,demonstrating rapid seawater degradation capability.
基金supported by the National Natural Science Foundation of China(Nos.22365026 and 21966028)the Science and Technology Project of Gansu(No.21YF5GA062)+3 种基金the Fundamental Research Funds for the Central Universities(Nos.31920220043,31920240094,and 31920230142)the Education Department of Gansu Province:Excellent Graduate student“Innovation Star”project(No.2023CXZX-202)Gansu Province Science Foundation for Youths(No.24JRRA160)the Funds for Special Projects of the Central Government in Guidance of Local Science and Technology Development(No.24ZY1QA026).
文摘The effective and environmentally friendly management of oily wastewater,alongside the beneficial conversion of waste biomass,holds paramount importance for environmental conservation,public health,and sustainable societal progress.In this research,an innovative biomass core-shell bioreactor(CGC@SiO_(2) aerogel) with selective adsorption and degradation properties was developed.The reactor's core is composed of coffee cellulose aerogel,offering a porous framework conducive to microbial colonization while safeguarding microorganisms from adverse external factors.The shell integrates hydrophobic silica enriched with polydimethylsiloxane,which alters the material's hydrophilic properties,enabling it to remain afloat on water for up to 100 days.This superhydrophobic layer maintained a contact angle of 150° even after ten consecutive rubbings.Experimental results indicate that the material performs exceptionally well in oil-water separation,as demonstrated by its success in 9 consecutive oil-water separations.It achieved 99 % selective adsorption,91 % removal,and 46.2 % degradation of a 3 wt.% diesel solution under conditions of 37℃,120 r/min,and pH=7.Additionally,tests assessing environmental tolerance revealed the material's robust adaptability and stability across varying pH levels and temperatures.Compared to traditional hydrophobic and lipophilic materials or free-floating microorganisms,CGC@SiO2 aerogel not only efficiently captures oil pollutants but also degrades them into non-hazardous substances.Combining biodegradation with selective adsorption has shown to be an effective approach for treating oily wastewater,offering significant practical application potential.The low-carbon production of CGC@SiO2aerogel aligns with circular economy principles,underscoring its role in sustainable development.
基金partly funded by the National Natural Science Foundation of China(62204098,62304124,62374105,22309107)Natural Science Foundation of Shandong Province(ZR2024QE036,ZR2024QB021,ZR2023QB281)+1 种基金Special Fund of Taishan Scholar Program of Shandong Province(tsqnz20221141)Qingdao Natural Science Foundation(24-4-4-zrjj-21-jch,25-1-1-114-zyydjch)。
文摘As one photovoltaic supernova,perovskite solar cells(PSCs)have exhibited certified power conversion efficiencies exceeding 27%.Yet,the presence of enormous defects,mainly for the dominant iodine vacancy(VI),always induces nonradiative recombination,ion migration,and triggers autocatalytic iodine oxidation into volatile I_(2) and charge-localization-mediated metallic Pb0clusters,which accelerate device failure and therefore hamper commercialization.However,popularly reported strategies that simultaneously enable vacancy passivation and iodine scavenging remain insufficient,highlighting the need for new additives.Herein,we employ 4-cyanophenylhydrazine hydrochloride(CPHCl)as an iodine-related synergistic redox-coordination stabilizer to address intrinsic instability and interface chemistry issues.After systematically characterizations,we demonstrate that CPHCl not only specifically eliminates I_(2) intermediates by leveraging the redox-active hydrazine group(NH–NH_(2))(I_(2)+NH–NH_(2)→2HI+N=NH),but also passivates Pb^(2+)/FA^(+) related defects viaπ-backdonation and hydrogen bonding by the electron-donating cyano(C≡N)group,synergistically modulating the crystallization kinetics and improving the final quality of the perovskite film.As a result,vacancy-mediated I-ion migration and degradation are significantly relieved,enabling an enhanced efficiency of 25.56%for the p-i-n inverted PSC with exceptional operational stability.This work provides a deep insight into screening perovskite stabilizers for advancing toward commercial longevity.
基金supported by the National Natural Science Foundation of China (No. 82304306)the Hubei Key Laboratory of Kidney Disease Occurrence and Intervention Development Fund (No. 2023SB108)+4 种基金the Huangshi City Science and Innovation Team Project of China (CXPT2023000002)the talent introduction program from Hubei Polytechnic University (No.19XJK07R)the Department of Education of Hubei Provincial Science and Technology Research Project (No. D20234502)the PostDoctoral Research Start-up Fund of Lishui People's Hospital, Zhejiang, China (2023bsh002)the Zhejiang Provincial Postdoctoral Research Project of Meritorious Support (ZJ2024007)。
文摘Molecular glues(MGs), a class of small-molecule degraders, exhibit drug-like properties that generally conform to Lipinski's rule of five, while uniquely mediating the stabilization or induction of protein-protein interactions. By altering the surface properties of either target proteins or E3 ligases, MGs promote the formation of a ternary complex comprising the MG, an E3 ligase, and a target protein. This interaction facilitates the polyubiquitination and subsequent degradation of the target protein via the ubiquitin-proteasome system.Owing to its distinctive mechanism of action and broad therapeutic potential, MG is offering novel approaches to disease treatment. This review summarizes recent advances in MGs targeting NEK7, WEE1, CDK2, GSPT1 and VAV1, emphasizing the rational design, benefits,and potential limitations, highlighting rational design principles, advantages, and current limitations including challenges in achieving selectivity and rational design that provide critical insights for enhancing MG efficacy. These developments are crucial for advancing the application and optimization of molecular glues targeting NEK7, WEE1, CDK2, GSPT1and VAV1.
基金National Natural Science Foundation of China(Nos.42177405,42377359,12075152)Energy Science and Technology discipline under the Shanghai Class IV Peak Disciplinary Development Program for the financial support.W.Y.Huang thanks the China Scholarship Council(CSC)for funding.
文摘Antibiotics are emerging pollutants that pose significant risks to environmental and human health.Periodate(PI)-based advanced oxidation processes have shown promise for their effective degradation.In this study,we systematically investigate the structure-activity relationship of four representative Fe-based metal-organic frameworks(Fe-MOFs)-MIL-101(Fe),MIL-88B(Fe),MIL-88A(Fe),and MIL-53(Fe)-as PI activators for tetracycline(TC)degradation.Among them,MIL-101(Fe)exhibited the highest catalytic performance,owing to its unique Fe3O-OH nodes and mesoporous architecture.The MIL-101(Fe)/PI system achieved 93.3%TC degradation and 55.9%mineralization rate within 60 min.Mechanistic studies combining scavenger quenching,sulfoxide probe transformation,X-ray photoelectron spectroscopy,and X-ray absorption fine structure confirmed the generation of multiple reactive oxygen species,and high-valent Fe(IV)]O and O_(2)^(·-)played major roles in the tetracycline degradation process.Density functional theory calculations further revealed that MIL-101(Fe)and MIL-88B(Fe)effectively interact with PI to form Fe(Ⅲ)-superoxide(Fe(Ⅲ)-O-O^(·-)),a key intermediate in Fe(IV)]O generation.In contrast,the adsorption energy of MIL-53(Fe)and MIL-88A(Fe)was relatively weak,with fewer binding sites,resulting in poor performance.The synergy between Fe(Ⅲ)-O-O^(·-)formation and the pore accessibility of MIL-101(Fe)accounted for its superior catalytic efficiency.This work not only clarifies the structural factors governing PI activation in Fe-MOFs,but also proposes a mechanistically informed strategy for designing high-performance catalysts for antibiotic degradation.
基金supported byHainan Provincial Natural Science Foundation of China(Nos.422RC600,519QN175)National Natural Science Foundation ofChina(Nos.52160018,21801053,52400206,52500209)High-Level Talent Program of Hainan Province(Nos.XJ2400008202,XJ2400011473).
文摘Oxidative magnetization has attracted great attention as an efficient strategy for modulating physiochemical properties of magnetic biochar.In this paper,a K_(2)FeO_(4)-involving hydrothermal oxidative magnetization was explored to regulate multiple micro-structures for manufacture magnetic hydrochar(MHC)for Fenton-like degradation of tetracycline in aqueous solution.Diverse shapes of Fe_(3)O_(4) and nano zero-valent iron(nZVI)were doped with abundant oxygen containing groups and persistent free radicals(PFRs).Multiple catalysis sites including iron species,PFRs,oxygen containing groups,and graphite defects contributed to accelerate the Fenton-like degradation with synergistic effect.Notably,MHC achieved a tetracycline removal rate of 99% within 60 min at 50 mg/L,with a total organic carbon(TOC)removal rate of 35%.Furthermore,after four cycles of reuse,the degradation efficiency slightly decreased to 93%.This study highlights the potential of magnetic hydrochar with multiple catalytic sites in the effective and sustainable degradation of pollutants.
基金support from the Australian Research Council projects(IC230100042).
文摘Hydrogel zinc ion batteries(HZIBs)represent a cutting-edge advancement in energy storage systems,leveraging the exceptional properties of hydrogels,including superior mechanical flexibility and robust structural stability.Despite their promising attributes,HZIBs face persistent challenges that hinder their practical deployment,notably performance degradation during long-term cycling.In this review,we provide a comprehensive explanation of the fundamental structure and working principles of HZIBs,analyzing the roles of each component.We then systematically explore these degradation mechanisms and comprehensively summarize the key influencing factors,including zinc dendrite formation,hydrogel matrix degradation,electrolyte depletion,and interfacial instability.The role of environmental and operational factors,such as temperature fluctuations and humidity variations,in exacerbating these degradation processes is also highlighted.Recent material engineering strategies to mitigate these issues are summarized:1)the development of structurally reinforced hydrogel electrolytes;2)the use of functional additives for ion transport regulation;and 3)interfacial engineering for uniform zinc deposition.Moreover,emerging fabrication techniques,such as nanoscale structural design and additive manufacturing,are discussed for their potential to optimize the mechanical robustness and electrochemical performance of HZIBs.This review integrates fundamental insights with advanced engineering approaches to provide practical guidance for the scalable development of high performance HZIBs for flexible and wearable applications.
基金supported by the National Natural Science Foundation of China (No.52370174)the Natural Science Foundation of Shandong Province,China (No.ZR2022ME128)Special Projects in Key Areas of Colleges and Universities in Guangdong Province (No.2023ZDZX4050)。
文摘The excessive use of pesticides has exacerbated environmental pollution due to herbicide residues,while their persistent toxicity poses serious challenges to global ecological security.A magnetically recyclable CoFe_(2)O_(4)/BiOBr S-scheme heterojunctions was prepared by microwave-assisted co-precipitation method for photocatalytic degradation of Diuron(DUR) in water.The formation of S-scheme heterojunction enhances electron transfer and charge separation,which was demonstrated by free radical trapping,electrochemical experiments,and DFT calculations.The magnetic CoFe_(2)O_(4)/BiOBr catalysts can achieve 99.9 %removal of diuron in 50 min under visible light irradiation.Furthermore,the system maintains stable performance across a broad p H range(3-9),enabling adaptation to diverse water environments,effective elimination of multiple pollutants,and strong resistance to ionic interference.Using magnetic recovery,CoFe_(2)O_(4)/BiOBr exhibits a high removal rate of 99 % and a markedly low ion leaching rate(<20 μg/L) after six cycles photocatalytic process,confirming its excellent stability and durability.According to HPLCQTOF-MS and DFT calculation,the main ways of DUR degradation include dechlorinated hydroxylation,dealkylation and hydroxylation of aromatic ring and side chain.Toxicity analysis showed that the toxicity of the intermediates generated during degradation was generally lower than that of DUR.The magnetic CoFe_(2)O_(4)/BiOBr S-scheme heterojunction developed in this study exhibits excellent photocatalytic performance,high applicability,good stability,and durability,providing an effective magnetic for the removal of refractory pollutants.
文摘Rui Chena,b,Tangbing Cui a,b,∗a School of Biology and Biological Engineering,South China University of Technology,Guangzhou 510006,China b Guangdong Key Laboratory of Fermentation and Enzyme Engineering,South China University of Technology,Guangzhou 510006,China The authors regret that the published version of this article contained several errors and omissions,which are described and corrected below.1.Figs.3 and 4(figure order and legends).In the published article,Figs.3 and 4 were inadvertently published in reversed order.The figures should be swapped so that the figure content matches its caption.The correct figures and their legends are provided on the following page.2.Title correction.The compound name in the published title was incorrectly typeset as“benzo[a]pyrene”The correct spelling is“benzo[a]pyrene.”3.Text corrections in Section 2.4.Several typographical errors occurred in Section 2.4(“Up-regulation of acetoin,lactate,and kanosamine biosynthesis under sodium gluconate treatment”).
