Nitrogenous compounds(i.e.,amines,amides,nitriles,oximes,amino acids and nitrogen-heterocycles derivatives)are important building blocks for synthetic chemistry,pharmaceuticals,and functional materials.Conventional sy...Nitrogenous compounds(i.e.,amines,amides,nitriles,oximes,amino acids and nitrogen-heterocycles derivatives)are important building blocks for synthetic chemistry,pharmaceuticals,and functional materials.Conventional synthetic strategies involve the use of toxic organic nitrogenous precursors or expensive heterogeneous catalysts under elevated temperatures and pressurized oxygen.Heterogeneous electrocatalysis can initiate the activation of inorganic N sources(i.e.,NH_(3)and NO^(-)_(x))under ambient reactions in liquid phase by applying a small bias,thus allowing the synthesis of value?added nitrogenous compounds from carbonyls,alkenes,keto acids,and even carbon dioxide in a sustainable manner without the use of oxidants/reductants.This review outlines recent de-velopments in electrosynthesis of nitrogenous compounds using inorganic N sources,focusing on reaction mechanisms understanding,the design and optimization of efficient electrocatalysts,and the advances in cell configurations for various C‒N coupling reactions.The limitations and challenges in applications are also discussed.展开更多
The single-layer Ti_(3)C_(2)T_(x)/MXene has become a special electromagnetic wave absorber near the terahertz band because of its abundant surface groups and excellent conductivity.However,the macro-preparation of sin...The single-layer Ti_(3)C_(2)T_(x)/MXene has become a special electromagnetic wave absorber near the terahertz band because of its abundant surface groups and excellent conductivity.However,the macro-preparation of single-layer Ti_(3)C_(2)T_(x)/MXene shows significantly difficult to influence its application.The two-dimensional Ti_(3)C_(2)T_(x)is easily prepared to have high production,but its weak absorption ability due to high surface conductivity also restricts its application.To realize the strong electromagnetic wave absorption of two-dimensional Ti_(3)C_(2)T_(x)/MXene,a new strategy with magnetic FeNi nanoparticles decorating Ti_(3)C_(2)T_(x)/MXene composites(FeNi-Ti_(3)C_(2)T_(x))were proposed and the effective electromagnetic wave absorption features covering 170-220 GHz that means the absorption band width reach 50 GHz.With an absorber composite film thickness being only 0.6 mm,the absorptivity of the composite is enhanced with the increase of decorating FeNi nanoparticles and promote up to 75%when the FeNi nanoparticles loading content reaches 30 wt%.The improvement of absorption is attributed to the introduction of soft magnetic FeNi to adjust the high surface conductivity of MXene and improve the electromagnetic balance of the absorber.展开更多
Incorporating organic bulky cations in the precursor or post-treatment to achieve two-dimensional/thr ee-dimensional(2D/3D)heterojunction is an effective strategy for enhancing the stability of perovskite materials.Ho...Incorporating organic bulky cations in the precursor or post-treatment to achieve two-dimensional/thr ee-dimensional(2D/3D)heterojunction is an effective strategy for enhancing the stability of perovskite materials.However,the issue of insufficient charge transport in 2D perovskites limits their development,and the fundamental mechanism of out-of-plane carrier transport remains unclear.This study designed and synthesized seven organic phenyl-core cations,differentiated at the 1-and 1,4-positions,and identified the impacts on the corresponding properties of the 2D crystalline perovskite.Shorter cations facilitated a more compact arrangement of adjacent inorganic layers,aligning to favor charge transport along the vertical direction.In addition,introducing high electronegativity led to increased intermolecular interactions,resulting in enhanced structural stability and improved phenyl ring π-orbital overlap and interlayer electron coupling,yielding efficient charge transport.Resilience to thermal stressing of the perovskite was strongly correlated with the carbon chain length of the spacer cations.The increase in cation length and the reduction in the rigidity of the amino-terminal both aided in the dispersion of thermal stress in the inorganic framework.Additional hydrogen bonding also contributed to mitigating structural disorder.展开更多
Microneedle(MN)patches could be a promising treatment for diabetic foot ulcers that plague thousands of people worldwide.While reducing skin resistance or increasing driving force can accelerate the efficiency of tran...Microneedle(MN)patches could be a promising treatment for diabetic foot ulcers that plague thousands of people worldwide.While reducing skin resistance or increasing driving force can accelerate the efficiency of transdermal drug delivery with conventional MN patches,it can create toxic chemical residues or require the help of additional devices.Herein,a thermo-responsive microneedles patch(TMN)with high biocompatibility without additional equipment is proposed.The TMN consisted of a bilayer microneedles composed of sodium alginate(SA)-g-poly(N-isopropylacrylamide)layer(SA-g-PNIPAM)loaded with sucrose octasulfate sodium salt(SOS)and hyaluronic acid layer and a polycaprolactone/chitosan nanofiber membrane loading with tetracycline hydrochloride(TH)and SOS.PNIPAM accelerates drug release by extruding the drug through a volumetric phase transition in response to temperature changes,and TH and SOS promote wound healing by inhibiting bacterial growth and promoting vascular regeneration and epithelial formation.The results showed that the drug release of TMN was significantly faster,with the drug release rate of more than 80% in the 10th h,and the antibacterial rate of TMN could reach 800%.In addition,TMN had good biocompatibility and good healing effects in vivo,which may be helpful for the design of multifunctional dressings in the future.展开更多
PbSe materials,with their narrow bandgap,excellent optical absorption and outstanding optical response,are ideal for infrared photodetectors,exhibiting unique advantages in optical communication,infrared imaging and t...PbSe materials,with their narrow bandgap,excellent optical absorption and outstanding optical response,are ideal for infrared photodetectors,exhibiting unique advantages in optical communication,infrared imaging and thermal detection.Nevertheless,PbSe typically has a non-layered crystal structure and inherent isotropy,making the synthesis of low-dimensional nanomaterials challenging.Besides,PbSe photoconductive detectors suffer from high dark current due to intrinsic defects and thermally excited carriers,which is detrimental to device performance.Here,we utilized physical vapor deposition(PVD)method to grow high-quality PbSe nanosheets and combined them with two-dimensional(2D)transition metal dichalcogenides(TMDs)material WSe_(2)to fabricate a self-powered PbSe/WSe_(2)p-n heterostructure photodetector.Under illumination with a 650 nm laser at a power density of 128.97 mW/cm^(2)and 0 V bias,the PbSe/WSe_(2)heterojunction device exhibited significant photovoltaic characteristics and generated a short-circuit current of 161.7 nA.Furthermore,under 0.02 mW/cm^(2)of 650 nm laser illumination at 0 V bias,the device achieved an excellent responsivity(R)of 15.6 A/W and a specific detectivity(D^(*))of 1.08×10^(11)Jones.And the response speed of the heterojunction device at 0 V(511µs/74µs)was three orders of magnitude faster than that of PbSe nanosheets(93 ms/104 ms).The device also demonstrated broadband detection capabilities from 405 nm to 1550 nm and excellent imaging performance in the near-infrared region at 0 V bias.In summary,the outstanding photoelectric detection performance and imaging capabilities of the PbSe/WSe_(2)heterojunction nanosheet detector indicate its significant potential for applications in miniaturized,low-noise,broadband,high-speed and high-performance photodetectors.展开更多
Harnessing photocatalyzed hydrogen atom transfer(HAT)for the precise activation of C–H/O–H bonds is a pivotal yet challenging strategy to selectively drive oxidative C–C bond scission in renewable lignin,yielding v...Harnessing photocatalyzed hydrogen atom transfer(HAT)for the precise activation of C–H/O–H bonds is a pivotal yet challenging strategy to selectively drive oxidative C–C bond scission in renewable lignin,yielding value-added chemicals with exceptional selectivity.Herein,we present a metal-free photochemical strategy that enables selective C–C bond scission in lignin via a unique synergistic HAT pathway driven by triplet-excited 2-ethylanthraquinone(EAQ^(*))and hydroxyl radicals(•OH)generated in situ from EAQH_(2) and O_(2).Under simulated natural conditions,this process achieves a benzaldehyde yield of 146.6 mol%from a lignin-derived phenolic dimer.Mechanistic investigations reveal that preferential activation of the Cα-OH in lignin facilitates a tandem HAT process,forming alkoxy radical intermediates that undergoβ–scission to produce benzaldehyde,as corroborated by extensive control reactions and density functional theory calculations.Furthermore,this straightforward protocol efficiently cleaves the C–C bonds of technical kraft lignins,providing a rapid,scalable,and metal-free protocol for lignin valorization under mild conditions.展开更多
The caries-preventive effects of arginine have been attributed to its impact on biofilm composition and pH.Recent in vitro studies suggest that arginine also affects the production of biofilm matrix components that co...The caries-preventive effects of arginine have been attributed to its impact on biofilm composition and pH.Recent in vitro studies suggest that arginine also affects the production of biofilm matrix components that contribute to virulence,but this mechanism has not been investigated clinically.This randomized,placebo-controlled,triple-blind,split-mouth in situ trial assessed arginine's impact on the microbial composition,matrix architecture,and microscale pH of biofilms from caries-active patients(N=10).We also examined whether individual differences in the pH response to arginine were related to biofilm composition and matrix structure.Biofilms were grown for four days on carriers attached to intraoral splints.Three times daily,the biofilms were treated extraorally with sucrose(5 min),followed by arginine or placebo(30 min),in a split-mouth design.After growth,the microscale biofilm p H response to sucrose was monitored by pH ratiometry.Microbial biofilm composition and carbohydrate matrix architecture were analyzed by 16S rRNA gene sequencing and fluorescence lectin-binding analysis,respectively.Arginine treatment significantly mitigated sucrose-induced pH drops,reduced total carbohydrate matrix production,and altered the spatial distribution of fucoseand galactose-containing carbohydrates.Both arginine-and placebo-treated biofilms were dominated by streptococci and Veillonella spp.Paired analyses showed a significant reduction in mitis/oralis group streptococci and a non-significant increase in several arginine metabolizers in arginine-treated biofilms.Individual pH responses were not significantly associated with the abundance of specific bacterial taxa or carbohydrate matrix components.In conclusion,arginine reduced the virulence of biofilms from caries-active patients through multiple mechanisms,including suppressing matrix carbohydrate production.展开更多
Metal-carbon dioxide(CO_(2))batteries hold great promise for reducing greenhouse gas emissions and are regarded as one of the most promising energy storage techniques due to their efficiency advantages in CO_(2)recove...Metal-carbon dioxide(CO_(2))batteries hold great promise for reducing greenhouse gas emissions and are regarded as one of the most promising energy storage techniques due to their efficiency advantages in CO_(2)recovery and conversion.Moreover,rechargeable nonaqueous metal-CO_(2)batteries have attracted much attention due to their high theoretical energy density.However,the stability issues of the electrode-electrolyte interfaces of nonaqueous metal-CO_(2)(lithium(Li)/sodium(Na)/potassium(K)-CO_(2))batteries have been troubling its development,and a large number of related research in the field of electrolytes have conducted in recent years.This review retraces the short but rapid research history of nonaqueous metal-CO_(2)batteries with a detailed electrochemical mechanism analysis.Then it focuses on the basic characteristics and design principles of electrolytes,summarizes the latest achievements of various types of electrolytes in a timely manner and deeply analyzes the construction strategies of stable electrode-electrolyte interfaces for metal-CO_(2)batteries.Finally,the key issues related to electrolytes and interface engineering are fully discussed and several potential directions for future research are proposed.This review enriches a comprehensive understanding of electrolytes and interface engineering toward the practical applications of next-generation metal-CO_(2)batteries.展开更多
Catalytic activity and hydrothermal stability are both crucial for the application of the selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR)catalyst in diesel vehicles.In this study,a tin(Sn)-modified Ce-N...Catalytic activity and hydrothermal stability are both crucial for the application of the selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR)catalyst in diesel vehicles.In this study,a tin(Sn)-modified Ce-Nb mixed-oxide catalyst was synthesized as an NH_(3)-SCR catalyst for NO_(x)emission control.After the intro-duction of Sn,both the NH_(3)-SCR activity and the hydrothermal stability of the catalyst were remarkably promoted.Even after hydrothermal aging at 1000℃,the developed Ce_(1)Sn_(2)Nb_(1)O_(x)catalyst achieved more than 90%NO_(x)conversion at 325-500℃.Various methods,including N2-physisorption,X-ray diffraction,in-situ high-temperature X-ray diffraction,high-resolution transmission electron microscopy,X-ray pho-toelectron spectroscopy,X-ray absorption fine-structure spectroscopy,temperature-programmed reduc-tion of hydrogen,temperature-programmed desorption of ammonia,and density functional theory calculations were used to investigate the promotional effects induced by the Sn species.The characteri-zation results showed that the addition of Sn not only promoted the formation of the Ce-Nb active phase but also improved its thermal stability,contributing to the excellent NH_(3)-SCR performance and hydrothermal stability.This study provides an excellent sintering-resistance catalyst for the application of diesel engine NO_(x)emission control.展开更多
Rh single atom catalysts(SACs)have been insensitively investigated recently due to the maximum utilization efficiency of Rh,one of the most expensive precious metals.Although great efforts have been made in the develo...Rh single atom catalysts(SACs)have been insensitively investigated recently due to the maximum utilization efficiency of Rh,one of the most expensive precious metals.Although great efforts have been made in the development and application of Rh SACs,there are few reports on the precise control of the local coordination environment of Rh single sites on CeO_(2) and their catalytic performance for N_(2)O decomposition.Herein,Rh/CeO_(2) catalysts with different Rh-O coordination numbers(CNs)were successfully prepared using different CeO_(2) supports and a simple incipient wetness impregnation(IWI)method.It is observed that the Rh/CeO_(2) catalyst with slightly higher CN of Rh-O(Rh/CeO_(2)-H)prepared from CeO_(2) shows much higher N_(2)O decomposition activity than the catalyst with lower CN of Rh-O(Rh/CeO_(2)-L)obtained from Ce(OH)_(x).The Rh species within Rh/CeO_(2)-H are found to be more reactive than those within Rh/CeO_(2)-L,which can better facilitate the O_(2)desorption once formed during N_(2)O deco mposition.In additio n,more surface oxygen vacancies are present on Rh/CeO_(2)-H than on Rh/CeO_(2)-L,well explaining the superior N_(2)O adsorption and activation capability on the former catalyst.It is concluded that more abundant oxygen vacancies and reactive Rh single atom sites with slightly higher CN of Rh-O and significantly higher reducibility altogether contribute to the superior N_(2)O decomposition activity on the Rh/CeO_(2)-H catalyst.展开更多
As a new member in two-dimensional materials family,transition metal carbides(TMCs)have many excellent properties,such as chemical stability,in-plane anisotropy,high conductivity and flexibility,and remarkable energy ...As a new member in two-dimensional materials family,transition metal carbides(TMCs)have many excellent properties,such as chemical stability,in-plane anisotropy,high conductivity and flexibility,and remarkable energy conversation efficiency,which predispose them for promising applications as transparent electrode,flexible electronics,broadband photodetectors and battery electrodes.However,up to now,their device applications are in the early stage,especially because their controllable synthesis is still a great challenge.This review systematically summarized the state-of-the-art research in this rapidly developing field with particular focus on structure,property,synthesis and applicability of TMCs.Finally,the current challenges and future perspectives are outlined for the application of 2D TMCs.展开更多
As an outstanding representative of layered materials,molybdenum disulfide(MoS_(2))has excellent physical properties,such as high carrier mobility,stability,and abundance on earth.Moreover,its reasonable band gap and ...As an outstanding representative of layered materials,molybdenum disulfide(MoS_(2))has excellent physical properties,such as high carrier mobility,stability,and abundance on earth.Moreover,its reasonable band gap and microelectronic compatible fabrication characteristics makes it the most promising candidate in future advanced integrated circuits such as logical electronics,flexible electronics,and focal-plane photodetector.However,to realize the all-aspects application of MoS_(2),the research on obtaining high-quality and large-area films need to be continuously explored to promote its industrialization.Although the MoS_(2)grain size has already improved from several micrometers to sub-millimeters,the high-quality growth of wafer-scale MoS_(2)is still of great challenge.Herein,this review mainly focuses on the evolution of MoS_(2)by including chemical vapor deposition,metal–organic chemical vapor deposition,physical vapor deposition,and thermal conversion technology methods.The state-of-the-art research on the growth and optimization mechanism,including nucleation,orientation,grain,and defect engineering,is systematically summarized.Then,this review summarizes the wafer-scale application of MoS_(2)in a transistor,inverter,electronics,and photodetectors.Finally,the current challenges and future perspectives are outlined for the wafer-scale growth and application of MoS_(2).展开更多
Metal selenides,such as NiSe2,have exhibited great potentials as multifunctional materials for energy storage and conversation.However,the utilization of pure NiSe2 as electrode materials is limited by its poor cyclin...Metal selenides,such as NiSe2,have exhibited great potentials as multifunctional materials for energy storage and conversation.However,the utilization of pure NiSe2 as electrode materials is limited by its poor cycling stability,low electrical conductivity,and insufficient electrochemically active sites.To remedy these defects,herein,a novel NiSe2/Ti3C2Tx hybrid with strong interfacial interaction and electrical properties is fabricated,by wrapping NiSe2 octahedral crystal with ultrathin Ti3C2Tx MXene nanosheet.The NiSe2/Ti3C2Tx hybrid exhibits excellent electrochemical performance,with a high specific capacitance of 531.2 Fg-1 at1 A g-1 for supercapacitor,low overpotential of 200 mV at 10 mA g-1,and small Tafel slope of 37.7 mV dec-1 for hydrogen evolution reaction(HER).Furthermore,greater cycling stabilities for NiSe2/Ti3C2Tx hybrid in both supercapacitor and HER have also been achieved.These significant improvements compared with unmodified NiSe2 should be owing to thestrong interfacial interaction between NiSe2 octahedral crystal and Ti3C2Tx MXene,which provides enhanced conductivity,fast charge transfer as well as abundant active sites,and highlight the promising potentials in combinations of MXene with metal selenides for multifunctional applications such as energy storage and conversion.展开更多
Immobilizing metal atoms by multiple nitrogen atoms has triggered exceptional catalytic activity toward many critical electrochemical reactions due to their merits of highly unsaturated coordination and strong metal-s...Immobilizing metal atoms by multiple nitrogen atoms has triggered exceptional catalytic activity toward many critical electrochemical reactions due to their merits of highly unsaturated coordination and strong metal-substrate interaction.Herein,atomically dispersed Fe-NC material with precise sulfur modification to Fe periphery(termed as Fe-NSC) was synthesized,X-ray absorption near edge structure analysis confirmed the central Fe atom being stabilized in a specific configuration of Fe(N3)(N-C-S).By enabling precisely localized S doping,the electronic structure of Fe-N4 moiety could be mediated,leading to the beneficial adjustment of absorption/desorption properties of reactant/intermediate on Fe center.Density functional theory simulation suggested that more negative charge density would be localized over Fe-N4 moiety after S doping,allowing weakened binding capability to *OH intermediates and faster charge transfer from Fe center to O species.Electrochemical measurements revealed that the Fe-NSC sample exhibited significantly enhanced oxygen reduction reaction performance compared to the S-free Fe-NC material(termed as Fe-NC),showing an excellent onset potential of 1.09 V and half-wave potential of 0.92 V in 0.1 M KOH.Our work may enlighten relevant studies regarding to accessing improvement on the catalytic performance of atomically dispersed M-NC materials by managing precisely tuned local environments of M-Nx moiety.展开更多
Alcohol fuel electro-reforming is promising for green hydrogen generation while developing efficient bifunctional catalysts for alcohol fuel electrolysis is still very tricky.Herein,we for the first time proposed the ...Alcohol fuel electro-reforming is promising for green hydrogen generation while developing efficient bifunctional catalysts for alcohol fuel electrolysis is still very tricky.Herein,we for the first time proposed the electron-enriched Pt induced by CoSe_(2)has an efficient bi-functional catalytic ability for alcohol fuels electro-reforming of hydrogen in acid electrolytes.The theoretical calculation revealed the advantages of electron-enriched Pt surface for the adsorption of intermediate,which is well supported by spectroscopic analysis and CO-stripping techniques.Largely improved catalytic performances of activity,durability,and kinetics are demonstrated compared to the conventional alloy system and commercial Pt/C catalyst,due to the efficient synergism of Pt and CoSe_(2);the peak current density of Pt/CoSe_(2)for methanol(ethanol)oxidation is 87.61(48.27)m A cm^(-2),which is about 3.3(2.0)times higher than that of Pt/C catalyst and 2.0(1.5)times that of the traditional PtCo alloy catalysts.Impressively,about 80%of the initial current was found after 1000 cycles of stability test for alcohol fuel oxidation of Pt/CoSe_(2)catalyst,higher than that of Pt/C(ca.50%)and PtCo catalyst(65%).When Pt/CoSe_(2)catalyst serviced as bi-functional catalysts for electrolyzer,a low cell potential of 0.65(0.78)V for methanol(ethanol)electrolysis was required to reach 10 m A cm^(-2),which was about 1030(900)m V less than that of conventional water electrolysis using Pt/C as the catalyst.The current result is instructive for the design of novel bifunctional catalyst and the understanding of hydrogen generation via alcohol fuel electro-reforming.展开更多
Direct liquid fuel cells(DLFCs) have received increasing attention because of their high energy densities,instant recharging abilities, simple cell structure, and facile storage and transport. The main challenge for t...Direct liquid fuel cells(DLFCs) have received increasing attention because of their high energy densities,instant recharging abilities, simple cell structure, and facile storage and transport. The main challenge for the commercialization of DLFCs is the high loading requirement of platinum group metals(PGMs) as catalysts. Atomically dispersed catalysts(ADCs) have been brought into recent focus for DLFCs due to their well-defined active sites, high selectivity, maximal atom-utilization, and anti-poisoning property. In this review, we summarized the structure–property relationship for unveiling the underlying mechanisms of ADCs for DLFCs. More specifically, different types of fuels used in DLFCs such as methanol, formic acid,and ethanol were discussed. At last, we highlighted current challenges, research directions, and future outlooks towards the practical application of DLFCs.展开更多
A number of mitigation techniques exist to reduce the emissions of pollutant gases and greenhouse gases(GHGs) from anaerobic storage of livestock manure. Nanoparticle(NP)application is a promising mitigating treatment...A number of mitigation techniques exist to reduce the emissions of pollutant gases and greenhouse gases(GHGs) from anaerobic storage of livestock manure. Nanoparticle(NP)application is a promising mitigating treatment option for pollutant gases, but limited research is available on the mode of NP application and their effectiveness in gaseous emission reduction. In this study, zinc silica nanogel(ZnSNL), copper silica nanogel(CuSNL), and N-acetyl cysteine(NACL) coated zinc oxide quantum dot(Qdot) NPs were compared to a control lacking NPs. All three NPs tested significantly reduced gas production and concentrations compared to non-treated manure. Overall, cumulative gas volumes were reduced by 92.73%–95.83%, and concentrations reduced by 48.98%–99.75% for H_2S, and 20.24%–99.82% for GHGs. Thus, application of NPs is a potential treatment option for mitigating pollutant and GHG emissions from anaerobically stored manure.展开更多
基金the NSFC(No.22472112)the Suzhou Foreign Academician Workstation(No.SWY2022001)for financial supportsthe Soochow Municipal Laboratory for Low Carbon Technologies and Industries.
文摘Nitrogenous compounds(i.e.,amines,amides,nitriles,oximes,amino acids and nitrogen-heterocycles derivatives)are important building blocks for synthetic chemistry,pharmaceuticals,and functional materials.Conventional synthetic strategies involve the use of toxic organic nitrogenous precursors or expensive heterogeneous catalysts under elevated temperatures and pressurized oxygen.Heterogeneous electrocatalysis can initiate the activation of inorganic N sources(i.e.,NH_(3)and NO^(-)_(x))under ambient reactions in liquid phase by applying a small bias,thus allowing the synthesis of value?added nitrogenous compounds from carbonyls,alkenes,keto acids,and even carbon dioxide in a sustainable manner without the use of oxidants/reductants.This review outlines recent de-velopments in electrosynthesis of nitrogenous compounds using inorganic N sources,focusing on reaction mechanisms understanding,the design and optimization of efficient electrocatalysts,and the advances in cell configurations for various C‒N coupling reactions.The limitations and challenges in applications are also discussed.
基金supported by the National Key R&D Program of China(Nos.2023YFF0718303 and 2022YFB3504804)the National Natural Science Foundation of China(Nos.51871219,52031014 and 52401255)the Science and Technology Project of Shenyang City(No.22-101-0-27).
文摘The single-layer Ti_(3)C_(2)T_(x)/MXene has become a special electromagnetic wave absorber near the terahertz band because of its abundant surface groups and excellent conductivity.However,the macro-preparation of single-layer Ti_(3)C_(2)T_(x)/MXene shows significantly difficult to influence its application.The two-dimensional Ti_(3)C_(2)T_(x)is easily prepared to have high production,but its weak absorption ability due to high surface conductivity also restricts its application.To realize the strong electromagnetic wave absorption of two-dimensional Ti_(3)C_(2)T_(x)/MXene,a new strategy with magnetic FeNi nanoparticles decorating Ti_(3)C_(2)T_(x)/MXene composites(FeNi-Ti_(3)C_(2)T_(x))were proposed and the effective electromagnetic wave absorption features covering 170-220 GHz that means the absorption band width reach 50 GHz.With an absorber composite film thickness being only 0.6 mm,the absorptivity of the composite is enhanced with the increase of decorating FeNi nanoparticles and promote up to 75%when the FeNi nanoparticles loading content reaches 30 wt%.The improvement of absorption is attributed to the introduction of soft magnetic FeNi to adjust the high surface conductivity of MXene and improve the electromagnetic balance of the absorber.
基金financially supported by the Key Fund Project of Tianjin Natural Science Foundation(24JCZDJC00510)the Fundamental Research Funds for the Central Universitiespartially supported by the U.S.Department of Energy under Contract No.DE-AC3608GO28308 with Alliance for Sustainable Energy,Limited Liability Company(LLC),the Manager and Operator of the National Renewable Energy Laboratory,through Grant No.DE-SC0020718。
文摘Incorporating organic bulky cations in the precursor or post-treatment to achieve two-dimensional/thr ee-dimensional(2D/3D)heterojunction is an effective strategy for enhancing the stability of perovskite materials.However,the issue of insufficient charge transport in 2D perovskites limits their development,and the fundamental mechanism of out-of-plane carrier transport remains unclear.This study designed and synthesized seven organic phenyl-core cations,differentiated at the 1-and 1,4-positions,and identified the impacts on the corresponding properties of the 2D crystalline perovskite.Shorter cations facilitated a more compact arrangement of adjacent inorganic layers,aligning to favor charge transport along the vertical direction.In addition,introducing high electronegativity led to increased intermolecular interactions,resulting in enhanced structural stability and improved phenyl ring π-orbital overlap and interlayer electron coupling,yielding efficient charge transport.Resilience to thermal stressing of the perovskite was strongly correlated with the carbon chain length of the spacer cations.The increase in cation length and the reduction in the rigidity of the amino-terminal both aided in the dispersion of thermal stress in the inorganic framework.Additional hydrogen bonding also contributed to mitigating structural disorder.
基金supported by the Joint Funds of National Natural Science Foundation of China(No.U22A20162)the Natural Science Foundation of Hebei Province of China(No.C2021202002)+1 种基金the National Natural Science Foundation of China(No.52271245),the Natural Science Foundation of Tianjin(No.21JCQNJC01280)the financial support from the Danish Council for Independent Research(9040-00219B),European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement ENSIGN(Project ID:101086226),L4DNANO(Project ID:101086227).
文摘Microneedle(MN)patches could be a promising treatment for diabetic foot ulcers that plague thousands of people worldwide.While reducing skin resistance or increasing driving force can accelerate the efficiency of transdermal drug delivery with conventional MN patches,it can create toxic chemical residues or require the help of additional devices.Herein,a thermo-responsive microneedles patch(TMN)with high biocompatibility without additional equipment is proposed.The TMN consisted of a bilayer microneedles composed of sodium alginate(SA)-g-poly(N-isopropylacrylamide)layer(SA-g-PNIPAM)loaded with sucrose octasulfate sodium salt(SOS)and hyaluronic acid layer and a polycaprolactone/chitosan nanofiber membrane loading with tetracycline hydrochloride(TH)and SOS.PNIPAM accelerates drug release by extruding the drug through a volumetric phase transition in response to temperature changes,and TH and SOS promote wound healing by inhibiting bacterial growth and promoting vascular regeneration and epithelial formation.The results showed that the drug release of TMN was significantly faster,with the drug release rate of more than 80% in the 10th h,and the antibacterial rate of TMN could reach 800%.In addition,TMN had good biocompatibility and good healing effects in vivo,which may be helpful for the design of multifunctional dressings in the future.
基金supported financially by National Key Research and Development Program of China(No.2023YFB3611400)National Natural Science Foundation of China(Nos.62175026,62305047)+4 种基金China National Postdoctoral Program for Innovative Talents(No.BX20230059)China Postdoctoral Science Foundation(No.2023M740509)Guangdong Basic and Applied Basic Research Foundation(No.2024A1515010005)National Key Laboratory of Intense Pulsed Radiation Simulation and Effect Research Foundation(No.NKLIPR2315)Natural Science Foundation of Sichuan Province(No.24NSFSC1465).
文摘PbSe materials,with their narrow bandgap,excellent optical absorption and outstanding optical response,are ideal for infrared photodetectors,exhibiting unique advantages in optical communication,infrared imaging and thermal detection.Nevertheless,PbSe typically has a non-layered crystal structure and inherent isotropy,making the synthesis of low-dimensional nanomaterials challenging.Besides,PbSe photoconductive detectors suffer from high dark current due to intrinsic defects and thermally excited carriers,which is detrimental to device performance.Here,we utilized physical vapor deposition(PVD)method to grow high-quality PbSe nanosheets and combined them with two-dimensional(2D)transition metal dichalcogenides(TMDs)material WSe_(2)to fabricate a self-powered PbSe/WSe_(2)p-n heterostructure photodetector.Under illumination with a 650 nm laser at a power density of 128.97 mW/cm^(2)and 0 V bias,the PbSe/WSe_(2)heterojunction device exhibited significant photovoltaic characteristics and generated a short-circuit current of 161.7 nA.Furthermore,under 0.02 mW/cm^(2)of 650 nm laser illumination at 0 V bias,the device achieved an excellent responsivity(R)of 15.6 A/W and a specific detectivity(D^(*))of 1.08×10^(11)Jones.And the response speed of the heterojunction device at 0 V(511µs/74µs)was three orders of magnitude faster than that of PbSe nanosheets(93 ms/104 ms).The device also demonstrated broadband detection capabilities from 405 nm to 1550 nm and excellent imaging performance in the near-infrared region at 0 V bias.In summary,the outstanding photoelectric detection performance and imaging capabilities of the PbSe/WSe_(2)heterojunction nanosheet detector indicate its significant potential for applications in miniaturized,low-noise,broadband,high-speed and high-performance photodetectors.
文摘Harnessing photocatalyzed hydrogen atom transfer(HAT)for the precise activation of C–H/O–H bonds is a pivotal yet challenging strategy to selectively drive oxidative C–C bond scission in renewable lignin,yielding value-added chemicals with exceptional selectivity.Herein,we present a metal-free photochemical strategy that enables selective C–C bond scission in lignin via a unique synergistic HAT pathway driven by triplet-excited 2-ethylanthraquinone(EAQ^(*))and hydroxyl radicals(•OH)generated in situ from EAQH_(2) and O_(2).Under simulated natural conditions,this process achieves a benzaldehyde yield of 146.6 mol%from a lignin-derived phenolic dimer.Mechanistic investigations reveal that preferential activation of the Cα-OH in lignin facilitates a tandem HAT process,forming alkoxy radical intermediates that undergoβ–scission to produce benzaldehyde,as corroborated by extensive control reactions and density functional theory calculations.Furthermore,this straightforward protocol efficiently cleaves the C–C bonds of technical kraft lignins,providing a rapid,scalable,and metal-free protocol for lignin valorization under mild conditions.
基金supported by the Faculty of Health,Aarhus University,Denmark。
文摘The caries-preventive effects of arginine have been attributed to its impact on biofilm composition and pH.Recent in vitro studies suggest that arginine also affects the production of biofilm matrix components that contribute to virulence,but this mechanism has not been investigated clinically.This randomized,placebo-controlled,triple-blind,split-mouth in situ trial assessed arginine's impact on the microbial composition,matrix architecture,and microscale pH of biofilms from caries-active patients(N=10).We also examined whether individual differences in the pH response to arginine were related to biofilm composition and matrix structure.Biofilms were grown for four days on carriers attached to intraoral splints.Three times daily,the biofilms were treated extraorally with sucrose(5 min),followed by arginine or placebo(30 min),in a split-mouth design.After growth,the microscale biofilm p H response to sucrose was monitored by pH ratiometry.Microbial biofilm composition and carbohydrate matrix architecture were analyzed by 16S rRNA gene sequencing and fluorescence lectin-binding analysis,respectively.Arginine treatment significantly mitigated sucrose-induced pH drops,reduced total carbohydrate matrix production,and altered the spatial distribution of fucoseand galactose-containing carbohydrates.Both arginine-and placebo-treated biofilms were dominated by streptococci and Veillonella spp.Paired analyses showed a significant reduction in mitis/oralis group streptococci and a non-significant increase in several arginine metabolizers in arginine-treated biofilms.Individual pH responses were not significantly associated with the abundance of specific bacterial taxa or carbohydrate matrix components.In conclusion,arginine reduced the virulence of biofilms from caries-active patients through multiple mechanisms,including suppressing matrix carbohydrate production.
基金supports from the Beijing Laboratory of New Energy Storage Technology, North China Electric Power Universitythe Program of the National Energy Storage Industry-Education Platformthe Interdisciplinary Innovation Program of North China Electric Power University (No. XM2212315)
文摘Metal-carbon dioxide(CO_(2))batteries hold great promise for reducing greenhouse gas emissions and are regarded as one of the most promising energy storage techniques due to their efficiency advantages in CO_(2)recovery and conversion.Moreover,rechargeable nonaqueous metal-CO_(2)batteries have attracted much attention due to their high theoretical energy density.However,the stability issues of the electrode-electrolyte interfaces of nonaqueous metal-CO_(2)(lithium(Li)/sodium(Na)/potassium(K)-CO_(2))batteries have been troubling its development,and a large number of related research in the field of electrolytes have conducted in recent years.This review retraces the short but rapid research history of nonaqueous metal-CO_(2)batteries with a detailed electrochemical mechanism analysis.Then it focuses on the basic characteristics and design principles of electrolytes,summarizes the latest achievements of various types of electrolytes in a timely manner and deeply analyzes the construction strategies of stable electrode-electrolyte interfaces for metal-CO_(2)batteries.Finally,the key issues related to electrolytes and interface engineering are fully discussed and several potential directions for future research are proposed.This review enriches a comprehensive understanding of electrolytes and interface engineering toward the practical applications of next-generation metal-CO_(2)batteries.
基金supported by the National Natural Science Foundation of China(52225004 and 22276202)the National Key Research and Development Program of China(2022YFC3701804)the Youth Innovation Promotion Association of Chinese Academy of Sciences(2019045).
文摘Catalytic activity and hydrothermal stability are both crucial for the application of the selective catalytic reduction of NO_(x)with NH_(3)(NH_(3)-SCR)catalyst in diesel vehicles.In this study,a tin(Sn)-modified Ce-Nb mixed-oxide catalyst was synthesized as an NH_(3)-SCR catalyst for NO_(x)emission control.After the intro-duction of Sn,both the NH_(3)-SCR activity and the hydrothermal stability of the catalyst were remarkably promoted.Even after hydrothermal aging at 1000℃,the developed Ce_(1)Sn_(2)Nb_(1)O_(x)catalyst achieved more than 90%NO_(x)conversion at 325-500℃.Various methods,including N2-physisorption,X-ray diffraction,in-situ high-temperature X-ray diffraction,high-resolution transmission electron microscopy,X-ray pho-toelectron spectroscopy,X-ray absorption fine-structure spectroscopy,temperature-programmed reduc-tion of hydrogen,temperature-programmed desorption of ammonia,and density functional theory calculations were used to investigate the promotional effects induced by the Sn species.The characteri-zation results showed that the addition of Sn not only promoted the formation of the Ce-Nb active phase but also improved its thermal stability,contributing to the excellent NH_(3)-SCR performance and hydrothermal stability.This study provides an excellent sintering-resistance catalyst for the application of diesel engine NO_(x)emission control.
文摘实现绿色甲醇电解制氢需要高效的双功能催化剂。本文采用热处理结合乙二醇还原法成功制备了MoP-NC纳米球负载的超细Pt纳米粒子(平均粒径为2.53 nm)复合催化剂(Pt/MoP-NC)用于高效甲醇电解制氢。MoP-NC纳米球不仅能提高Pt纳米粒子的分散性并且增强Pt的抗中毒能力。电化学测试表明Pt/MoP-NC催化剂在酸性甲醇氧化反应(MOR)和析氢反应(HER)中具有较高的催化性能;其中,MOR的正向扫描峰值电流密度为90.7 m A·cm^(-2),是商业Pt/C催化剂的3.2倍,在10 mA·cm^(-2)的电流密度下,HER的过电位低至30 m V,与商业Pt/C接近。由Pt/MoP-NC||Pt/MoP-NC组装的两电极电解槽驱动10 mA·cm^(-2)的电流密度仅需要0.67 V的电压,比相同条件下电解水的电压低1.02 V,大大降低了能量输入。Pt/MoP-NC的高催化性能主要来源于Pt活性中心与相邻层状多孔球形结构的MoP-NC载体之间电子效应及配体效应引起的抗一氧化碳中毒能力的提升和含氧物种的容易生成。
基金supported by grants from International S&T Cooperation Program of China(2010DFA31710)The National Natural Science Foundation of China(11204267)The doctoral fund of innovation from Beijing University of Technology and by a grant from The Italian Association for Cancer Research(AIRC No IG 10412)~~
基金Project supported by the Startup Fund(F.L.)from the University of Central Florida(UCF)National Science Foundation grants(CHE-1955343,DMR-1920050).
文摘Rh single atom catalysts(SACs)have been insensitively investigated recently due to the maximum utilization efficiency of Rh,one of the most expensive precious metals.Although great efforts have been made in the development and application of Rh SACs,there are few reports on the precise control of the local coordination environment of Rh single sites on CeO_(2) and their catalytic performance for N_(2)O decomposition.Herein,Rh/CeO_(2) catalysts with different Rh-O coordination numbers(CNs)were successfully prepared using different CeO_(2) supports and a simple incipient wetness impregnation(IWI)method.It is observed that the Rh/CeO_(2) catalyst with slightly higher CN of Rh-O(Rh/CeO_(2)-H)prepared from CeO_(2) shows much higher N_(2)O decomposition activity than the catalyst with lower CN of Rh-O(Rh/CeO_(2)-L)obtained from Ce(OH)_(x).The Rh species within Rh/CeO_(2)-H are found to be more reactive than those within Rh/CeO_(2)-L,which can better facilitate the O_(2)desorption once formed during N_(2)O deco mposition.In additio n,more surface oxygen vacancies are present on Rh/CeO_(2)-H than on Rh/CeO_(2)-L,well explaining the superior N_(2)O adsorption and activation capability on the former catalyst.It is concluded that more abundant oxygen vacancies and reactive Rh single atom sites with slightly higher CN of Rh-O and significantly higher reducibility altogether contribute to the superior N_(2)O decomposition activity on the Rh/CeO_(2)-H catalyst.
基金This research was supported by grants from by the National Natural Science Foundation of China(52002254)Sichuan Science and Technology Program(2020YJ0262,2021YFH0127)+2 种基金Chunhui plan of Ministry of Education of China,Fundamental Research Funds for the Central Universities,China(YJ201893)State Key Lab of Advanced Metals and Materials,China(Grant No.2019-Z03)the Danish National Research Foundation and EU H2020RISE 2016-MNR4S Cell project.
文摘As a new member in two-dimensional materials family,transition metal carbides(TMCs)have many excellent properties,such as chemical stability,in-plane anisotropy,high conductivity and flexibility,and remarkable energy conversation efficiency,which predispose them for promising applications as transparent electrode,flexible electronics,broadband photodetectors and battery electrodes.However,up to now,their device applications are in the early stage,especially because their controllable synthesis is still a great challenge.This review systematically summarized the state-of-the-art research in this rapidly developing field with particular focus on structure,property,synthesis and applicability of TMCs.Finally,the current challenges and future perspectives are outlined for the application of 2D TMCs.
基金financially the National Natural Science Foundation of China(52002254,52272160)Sichuan Science and Technology Foundation(2020YJ0262,2021YFH0127,2022YFSY0045,2022YFH0083 and 23SYSX0060)+3 种基金the Chunhui plan of Ministry of Education,Fundamental Research Funds for the Central Universities,China(YJ201893)the Open-Foundation of Key Laboratory of Laser Device Technology,China North Industries Group Corporation Limited(Grant No.KLLDT202104)the foundation of the State Key Laboratory of Solidification Processing in NWPU(No.SKLSP202210)the 2035-Plan of Sichuan University。
文摘As an outstanding representative of layered materials,molybdenum disulfide(MoS_(2))has excellent physical properties,such as high carrier mobility,stability,and abundance on earth.Moreover,its reasonable band gap and microelectronic compatible fabrication characteristics makes it the most promising candidate in future advanced integrated circuits such as logical electronics,flexible electronics,and focal-plane photodetector.However,to realize the all-aspects application of MoS_(2),the research on obtaining high-quality and large-area films need to be continuously explored to promote its industrialization.Although the MoS_(2)grain size has already improved from several micrometers to sub-millimeters,the high-quality growth of wafer-scale MoS_(2)is still of great challenge.Herein,this review mainly focuses on the evolution of MoS_(2)by including chemical vapor deposition,metal–organic chemical vapor deposition,physical vapor deposition,and thermal conversion technology methods.The state-of-the-art research on the growth and optimization mechanism,including nucleation,orientation,grain,and defect engineering,is systematically summarized.Then,this review summarizes the wafer-scale application of MoS_(2)in a transistor,inverter,electronics,and photodetectors.Finally,the current challenges and future perspectives are outlined for the wafer-scale growth and application of MoS_(2).
基金supported by Grants from the Danish National Research FoundationAUFFNOVA project from Aarhus Universitets Forsknings fund,EU H2020RISE 2016-MNR4SCell project+4 种基金National Natural Science Foundation of China(Nos.21528501,51272296,and 51571195)the Chongqing Graduate Student Research Innovation Project(No.CYB15046)support from the Key Program of the Chinese Academy of Sciences(KJZD-EW-M05-3)the financial support of China Scholarship Council(CSC)the support of Fundamental Research Funds for the Central Universities,China(YJ201893)
文摘Metal selenides,such as NiSe2,have exhibited great potentials as multifunctional materials for energy storage and conversation.However,the utilization of pure NiSe2 as electrode materials is limited by its poor cycling stability,low electrical conductivity,and insufficient electrochemically active sites.To remedy these defects,herein,a novel NiSe2/Ti3C2Tx hybrid with strong interfacial interaction and electrical properties is fabricated,by wrapping NiSe2 octahedral crystal with ultrathin Ti3C2Tx MXene nanosheet.The NiSe2/Ti3C2Tx hybrid exhibits excellent electrochemical performance,with a high specific capacitance of 531.2 Fg-1 at1 A g-1 for supercapacitor,low overpotential of 200 mV at 10 mA g-1,and small Tafel slope of 37.7 mV dec-1 for hydrogen evolution reaction(HER).Furthermore,greater cycling stabilities for NiSe2/Ti3C2Tx hybrid in both supercapacitor and HER have also been achieved.These significant improvements compared with unmodified NiSe2 should be owing to thestrong interfacial interaction between NiSe2 octahedral crystal and Ti3C2Tx MXene,which provides enhanced conductivity,fast charge transfer as well as abundant active sites,and highlight the promising potentials in combinations of MXene with metal selenides for multifunctional applications such as energy storage and conversion.
基金supported by National Natural Science Foundation of China,Beijing University of Chemical Technology(buctrc201901)National Natural Science Foundation of China and Ministry of Foreign A airs and International Cooperation,Italy(NSFC–MAECI 51861135202)+4 种基金the National Key Research and Development Project(Grant No.2018YFB1502401,2018YFA0702002)the Royal Society and the Newton Fund through the Newton Advanced Fellowship award(NAF\R1\191294)the Program for Changjiang Scholars and Innovation Research Team in the University(No.IRT1205)the Fundamental Research Funds for the Central Universitiesthe long–term subsidy mechanism from the Ministry of Finance and the Ministry of Education of PRC。
文摘Immobilizing metal atoms by multiple nitrogen atoms has triggered exceptional catalytic activity toward many critical electrochemical reactions due to their merits of highly unsaturated coordination and strong metal-substrate interaction.Herein,atomically dispersed Fe-NC material with precise sulfur modification to Fe periphery(termed as Fe-NSC) was synthesized,X-ray absorption near edge structure analysis confirmed the central Fe atom being stabilized in a specific configuration of Fe(N3)(N-C-S).By enabling precisely localized S doping,the electronic structure of Fe-N4 moiety could be mediated,leading to the beneficial adjustment of absorption/desorption properties of reactant/intermediate on Fe center.Density functional theory simulation suggested that more negative charge density would be localized over Fe-N4 moiety after S doping,allowing weakened binding capability to *OH intermediates and faster charge transfer from Fe center to O species.Electrochemical measurements revealed that the Fe-NSC sample exhibited significantly enhanced oxygen reduction reaction performance compared to the S-free Fe-NC material(termed as Fe-NC),showing an excellent onset potential of 1.09 V and half-wave potential of 0.92 V in 0.1 M KOH.Our work may enlighten relevant studies regarding to accessing improvement on the catalytic performance of atomically dispersed M-NC materials by managing precisely tuned local environments of M-Nx moiety.
基金supported by the National Natural Science Foundation of China(21972124,22102105)a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutionthe support of the Six Talent Peaks Project of Jiangsu Province(XCL-070-2018)。
文摘Alcohol fuel electro-reforming is promising for green hydrogen generation while developing efficient bifunctional catalysts for alcohol fuel electrolysis is still very tricky.Herein,we for the first time proposed the electron-enriched Pt induced by CoSe_(2)has an efficient bi-functional catalytic ability for alcohol fuels electro-reforming of hydrogen in acid electrolytes.The theoretical calculation revealed the advantages of electron-enriched Pt surface for the adsorption of intermediate,which is well supported by spectroscopic analysis and CO-stripping techniques.Largely improved catalytic performances of activity,durability,and kinetics are demonstrated compared to the conventional alloy system and commercial Pt/C catalyst,due to the efficient synergism of Pt and CoSe_(2);the peak current density of Pt/CoSe_(2)for methanol(ethanol)oxidation is 87.61(48.27)m A cm^(-2),which is about 3.3(2.0)times higher than that of Pt/C catalyst and 2.0(1.5)times that of the traditional PtCo alloy catalysts.Impressively,about 80%of the initial current was found after 1000 cycles of stability test for alcohol fuel oxidation of Pt/CoSe_(2)catalyst,higher than that of Pt/C(ca.50%)and PtCo catalyst(65%).When Pt/CoSe_(2)catalyst serviced as bi-functional catalysts for electrolyzer,a low cell potential of 0.65(0.78)V for methanol(ethanol)electrolysis was required to reach 10 m A cm^(-2),which was about 1030(900)m V less than that of conventional water electrolysis using Pt/C as the catalyst.The current result is instructive for the design of novel bifunctional catalyst and the understanding of hydrogen generation via alcohol fuel electro-reforming.
基金financial supports from the National Science Foundation under Grant Nos. CBET-1949840 and CMMI-1851674financial support from the Preeminent Postdoctoral Program (P3) of the University of Central Florida。
文摘Direct liquid fuel cells(DLFCs) have received increasing attention because of their high energy densities,instant recharging abilities, simple cell structure, and facile storage and transport. The main challenge for the commercialization of DLFCs is the high loading requirement of platinum group metals(PGMs) as catalysts. Atomically dispersed catalysts(ADCs) have been brought into recent focus for DLFCs due to their well-defined active sites, high selectivity, maximal atom-utilization, and anti-poisoning property. In this review, we summarized the structure–property relationship for unveiling the underlying mechanisms of ADCs for DLFCs. More specifically, different types of fuels used in DLFCs such as methanol, formic acid,and ethanol were discussed. At last, we highlighted current challenges, research directions, and future outlooks towards the practical application of DLFCs.
文摘A number of mitigation techniques exist to reduce the emissions of pollutant gases and greenhouse gases(GHGs) from anaerobic storage of livestock manure. Nanoparticle(NP)application is a promising mitigating treatment option for pollutant gases, but limited research is available on the mode of NP application and their effectiveness in gaseous emission reduction. In this study, zinc silica nanogel(ZnSNL), copper silica nanogel(CuSNL), and N-acetyl cysteine(NACL) coated zinc oxide quantum dot(Qdot) NPs were compared to a control lacking NPs. All three NPs tested significantly reduced gas production and concentrations compared to non-treated manure. Overall, cumulative gas volumes were reduced by 92.73%–95.83%, and concentrations reduced by 48.98%–99.75% for H_2S, and 20.24%–99.82% for GHGs. Thus, application of NPs is a potential treatment option for mitigating pollutant and GHG emissions from anaerobically stored manure.
