The sluggish kinetics of the oxygen reduction reaction(ORR)and high over potential of oxygen evolution reaction(OER)are big challenges in the development of high-performance zinc-air batteries(ZABs)and fuel cells.In t...The sluggish kinetics of the oxygen reduction reaction(ORR)and high over potential of oxygen evolution reaction(OER)are big challenges in the development of high-performance zinc-air batteries(ZABs)and fuel cells.In this work,we report a rational design and a simple fabrication strategy of a photo-enhanced Co single-atom catalyst(SAC)comprising g-C3N4 coupled with cobalt-nitrogen-doped hierarchical mesoporous carbon(Co-N/MPC),forming a staggered p-n heterojunction that effectively improves charge separation and enhances electrocatalytic activity.The incorporation of Co SACs and g-C3N4 synergistically optimizes the photogenerated electron-hole pair separation,significantly boosting the intrinsic ORR-OER duplex activity.Under illumination,g-C_(3)N_(4)@Co-N/MPC exhibits an outstanding ORR half-wave potential(E1/2)of 0.841 V(vs.RHE)in 0.1 mol L^(–1)KOH and a low OER overpotential of 497.4 mV(vs.RHE)at 10 mA cm^(–2)in 1 mol L^(–1)KOH.Notably,the catalyst achieves an exceptional peak power density of 850.7 mW cm^(–2)in ZABs and of 411 mW cm^(–2)even in H_(2)-air fuel cell.In addition,g-C_(3)N_(4)@Co-N/MPC-based ZABs also show remarkable cycling stability exceeding 250 h.The advanced photo-induced charge separation at the p-n heterojunction facilitates faster electron transfer kinetics,and the mass transport owing to hierarchical mesoporous structure of Co-N-C,thereby reducing the overpotential and enhancing the overall energy conversion efficiency.This work provides a new perspective on designing next-generation of single-atom dispersed oxygen reaction catalysts,paving the way for high-performance photo-enhanced energy storage and conversion systems.展开更多
Synthesis of primary amines from alcohols is an economical and green route to access high-value N-compounds.However,challenges remain to develop both cost-effective and efficient catalysts.In this study,we developed a...Synthesis of primary amines from alcohols is an economical and green route to access high-value N-compounds.However,challenges remain to develop both cost-effective and efficient catalysts.In this study,we developed a Ru-Co/ZrO_(2)single-atom alloy catalyst which afforded diverse primary amines from alcohols in the presence of ammonia and hydrogen with exceptional conversion(up to 90%)and selectivity(80%)under mild conditions(0.7 MPa NH_(3),0.3 MPa H_(2),160℃)and exhibited satisfactory stability upon regeneration.The turnover rate was approximately 8.4 times higher than that observed over the Co/ZrO_(2)catalyst.Characterizations indicated that the alloyed Ru facilitated the reduction of Co,strengthened the interaction with H_(2)and mitigated the over-strong adsorption of aldehyde intermediates.These combined effects contributed significantly to the enhanced catalytic performances.This work presents a promising strategy for the development of advanced catalysts in the amination of alcohols.展开更多
Atomically dispersed single-atom catalysts(SACs)on carbon supports show great promise for H_(2)O_(2) electrosynthesis,but conventional wet chemistry methods using particulate carbon blacks in powder form have limited ...Atomically dispersed single-atom catalysts(SACs)on carbon supports show great promise for H_(2)O_(2) electrosynthesis,but conventional wet chemistry methods using particulate carbon blacks in powder form have limited their potential as two-electron(2^(e−))oxygen reduction reaction(ORR)catalysts.Here,we demonstrate high-performance Co SACs supported on a free-standing aligned carbon nanofiber(CNF)using electrospinning and arc plasma deposition(APD).Based on the surface oxidation treatment of aligned CNF and precise control of the deposition amount in a dry-based APD process,we successfully form densely populated Co SACs on aligned CNF.Through experimental analyses and density functional theory calculations,we reveal that Co SAC has a Co–N_(2)–O_(2) moiety with one epoxy group,leading to excellent 2^(e−)ORR activity.Furthermore,the aligned CNF significantly improves mass transfer in flow cells compared to randomly oriented CNF,showing an overpotential reduction of 30 mV and a 1.3-fold improvement(84.5%)in Faradaic efficiency,and finally achieves an outstanding production rate of 15.75 mol gcat^(−1) h^(−1) at 300 mA cm^(−2).The high-performance Co SAC supported on well-aligned CNF is also applied in an electro-Fenton process,demonstrating rapid removal of methylene blue and bisphenol F due to its exceptional 2e^(−)ORR activity.展开更多
Single-atom catalysts(SACs)have garnered tremendous and continuous attention in photocatalytic CO_(2)reduction reactions(CO_(2)RR),due to their compelling potential in broadening the light-harvesting range,elevating t...Single-atom catalysts(SACs)have garnered tremendous and continuous attention in photocatalytic CO_(2)reduction reactions(CO_(2)RR),due to their compelling potential in broadening the light-harvesting range,elevating the charge separation/transfer efficiency,and enhancing surface reaction.Despite the surge in research and the expanding range of potential central metal candidates—including d-block,p-block,and rare metal elements,etc.—the comprehension of the structure-function relationships between the central metal and its performance remains elusive.Hence,categorized by different areas of the central metal element from periodic table,we outline the recent progress and challenges on SACs for photocatalytic CO_(2)RR.We begin by describing various synthetic strategies employed for SACs.Subsequently,a clear classification of the SACs applications in photocatalytic CO_(2)RR is provided,according to the central metal elements in different blocks of the periodic table.We also discussed how isolated metal single-atom sites from different blocks of the periodic table improve the performance of photocatalytic CO_(2)reduction from the perspective of charge separation and transfer.Finally,we end this review with some perspectives and challenges associated with SACs for photocatalytic CO_(2)reduction.Through this review,we aim to enrich the element diversity of SACs for photocatalytic CO_(2)RR,reveal trends in element evolution,and propose directions for future development in this flourishing field.展开更多
Sluggish sulfur redox kinetics remain a critical bottleneck in the advancement of high-performance lithiumsulfur batteries(LSBs).Single-atom catalysts(SACs)offer a promising solution to this limitation,particularly wh...Sluggish sulfur redox kinetics remain a critical bottleneck in the advancement of high-performance lithiumsulfur batteries(LSBs).Single-atom catalysts(SACs)offer a promising solution to this limitation,particularly when their coordination structures are carefully engineered.Here,we develop a chromium-based SAC featuring a unique undercoordinated CrN_(3) configuration to boost sulfur electrochemistry.Compared with conventional CrN_(4),the CrN_(3) motif lowers 3d orbital occupancy and meanwhile activates the in-plane hybridizations with S 3p orbitals upon interaction with polysulfides,contributing to moderate adsorption strength and reduced energy barriers for bidirectional sulfur conversions.Additionally,the integration of the two-dimensional(2D)porous framework ensures abundant electrochemically active surfaces and efficiently exposed active sites.As a result,CrN_(3)-based cells demonstrate fast and durable sulfur redox reactions,enabling an ultralow capacity decay of 0.0075%per cycle over 1000 cycles and a high-rate capability of 651.9 mAh·g^(-1)at 5 C.The CrN_(3) catalyst retains robust catalytic efficiency under demanding conditions,delivering a high areal capacity of 5.53 mAh·cm^(-2) at high sulfur loading and lean electrolyte.This work establishes a compelling paradigm of SAC coordination engineering for designing advanced sulfur electrocatalysts for next-generation LSBs.展开更多
Oxygen reduction reaction(ORR)is crucial for Znair batteries,while also serves as a core electrochemical process in oxygen depolarized cathodes(ODCs)for chlor-alkali electrolysis.The lack of cost-effective,highly acti...Oxygen reduction reaction(ORR)is crucial for Znair batteries,while also serves as a core electrochemical process in oxygen depolarized cathodes(ODCs)for chlor-alkali electrolysis.The lack of cost-effective,highly active ORR electrocatalysts with superior kinetics hinders progress in this field.Herein,we report the Fe/Ni dual single-atomic sites anchored by commercial carbon black(Fe/Ni-N/CB)using rigid ligand confined and high-temperature shock(HTS)strategy in less than 0.5 s.Theoretical calculation reveals that singleatomic Fe is the real active site.Single-atomic Fe and Ni species in Fe/Ni-N/CB synergistically accelerate the kinetics of ORR by reducing the energy barrier of the rate-determining step.A large half-wave potential(E_(1/2))of 0.907 V is achieved in 0.1 M KOH aqueous solution.The assembled aqueous Zn-air battery(A-ZAB)with Fe/Ni-N/CB cathode presents remarkable charge-discharge cycling stability for over 650 h without voltage gap degradation.The quasi-solid-state Zn-air battery(QSS-ZAB)exhibits excellent reversibility over a 150-h operation at 0.5 mA·cm^(-2) with negligible energy conversion efficiency recession.Impressively,Fe/Ni-N/CB||RuO_(2)chloralkali flow cell exhibits a low cell voltage of 1.60 V at a large current density of 300 mA·cm^(-2) at 80℃,and demonstrates exceptional durability with 7% current density decay over 150 h of continuous operation at 100 mA·cm^(-2).Fe/Ni-N/CB||RuO_(2)achieves near-ideal caustic current efficiency(~97.2%)at the current density of 300 mA·cm^(-2).This work provides a rapid and economical synthesis technique for the synthesis of catalysts at the atomic scale while demonstrating significant potential for application in energy-saving chlor-alkali electrolyzer.展开更多
NO oxidation with H_(2)O_(2)as the oxidant is a promising green denitration technology.However,the current metal oxide catalysts still have many disadvantages for this reaction,such as insufficient catalytic activity ...NO oxidation with H_(2)O_(2)as the oxidant is a promising green denitration technology.However,the current metal oxide catalysts still have many disadvantages for this reaction,such as insufficient catalytic activity for H_(2)O_(2)activation,poor selectivity,and low stability.In this study,we employ atomically dispersed Co anchored on SBA-15 with Co-O_(4)structure for NO oxidation,which achieves a 90%removal efficiency of NO under low molar ratio of H_(2)O_(2)to NO(1.56),ultra-low temperature(80℃),and ultra-high space velocity(720,000 h^(-1)),representing the top-level performance among previously reported catalysts.More interestingly,our work reveals that by taking advantage of the uniform Co-O_(4)structure,H_(2)O_(2)is mainly directionally converted into·O_(2)^(-)at the Co-O_(4)site,and·O_(2)^(-)plays a key role for achieving the deep-oxidation of NO to produce NO_(3)^(-),which is contrast to the previously reports that^(1)O_(2)is the main free radical for NO oxidation.This study highlights the great potentials of single-atom catalysts for improving the H_(2)O_(2)utilization performance for NO oxidation.展开更多
Solving the problems of carbon dioxide(CO_(2))emissions and energy scarcity by the development of highly selective,cost-effective,and reliable catalysts for the electrochemical reduction of CO_(2)to useful carbon-base...Solving the problems of carbon dioxide(CO_(2))emissions and energy scarcity by the development of highly selective,cost-effective,and reliable catalysts for the electrochemical reduction of CO_(2)to useful carbon-based products would be very helpful.We report the synthesis of an efficient graphene-supported bismuth single-atom catalyst(BiSA-G)featuring a BiN_(4)coordination structure for this purpose.The synthesis used tannic acid as a multifunctional ligand and ammonia as a nitrogen dopant.Using a scalable coordination chemistry approach,BiN_(4)sites were uniformly dispersed on the graphene substrate and were found to have an outstanding ability for the conversion of CO_(2)to CO,with a high Faradaic efficiency of 97.4%at−0.55 V(vs.RHE)and a high turnover frequency of 5230 h^(−1)along with outstanding stability.Density functional theory calculations confirmed that the BiN_(4)site serves as the dominant active center,simultaneously facilitating CO_(2)activation and the efficient formation of the crucial intermediate*COOH with a reduced free energy barrier.This discovery offers a new way for the atomic-scale design of high-efficiency catalysts for the electrochemical CO_(2)reduction reaction,potentially helping sustainable carbon use.展开更多
In recent years,numer-ous single-atom catalysts(SACs)have been synthesized to activate persulfate(PS)by a non-radical pathway because of its high se-lectivity,and activity for the cata-lyst.Metal-nitrogen-carbon(M-N_(...In recent years,numer-ous single-atom catalysts(SACs)have been synthesized to activate persulfate(PS)by a non-radical pathway because of its high se-lectivity,and activity for the cata-lyst.Metal-nitrogen-carbon(M-N_(x)-C)has been identified as the key active site in SACs.Although methods for preparing SACs have been extensively reported,a systematic summary of the direct construction of M-N_(x)-C,espe-cially unconventional metal-nitrogen-carbon(UM-N_(x)-C,x≠4),on SACs for PS non-radical activation has still not been reported.The role of the M-N_(x)-C active sites on PS non-radical activation is discussed and methods for the formation of M-N_(x)-C and UM-N_(x)-C active sites in SACs and the effect of catalyst carriers such as carbon nitride(g-C_(3)N_(4)),MOFs,COFs,and other car-bon materials are reviewed.Direct and indirect methods,especially for UM-N_(x)-C active site formation,are also elaborated.Factors affecting the formation of a M-N_(x)-C active site on SACs are also discussed.Prospects for the use of M-N_(x)-C active sites for the non-radical activation of PS by SACs to remove organic contaminants from wastewater are evaluated.展开更多
By simplifying catalyst-product separation and reducing phosphorus waste,heterogeneous hydroformylation offers a more sustainable alternative to homogeneous processes.However,heterogeneous hydroformylation catalysts d...By simplifying catalyst-product separation and reducing phosphorus waste,heterogeneous hydroformylation offers a more sustainable alternative to homogeneous processes.However,heterogeneous hydroformylation catalysts developed thus far still suffer from the issues of much lower activity and metal leaching,which severely hinder their practical application.Here,we demonstrate that incorporating phosphorus(P)atoms into graphitic carbon nitride(PCN)supports facilitates charge transfer from Rh to the PCN support,thus largely enhancing electronic metal-support interactions(EMSIs).In the styrene hydroformylation reaction,the activity of Rh_(1)/PCN single-atom catalysts(SACs)with varying P contents exhibited a volcano-shaped relationship with P doping,where the Rh_(1)/PCN SAC with optimal P doping showed exceptional activity,approximately 5.8-and 3.3-fold greater than that of the Rh_(1)/g-C_(3)N_(4)SAC without P doping and the industrial homogeneous catalyst HRh(CO)(PPh_(3))_(3),respectively.In addition,the optimal Rh_(1)/PCN SAC catalyst also demonstrated largely enhanced multicycle stability without any visible metal aggregation owing to the increased EMSIs,which sharply differed from the severe metal aggregation of large nanoparticles on the Rh_(1)/g-C_(3)N_(4)SAC.Mechan-istic studies revealed that the enhanced catalytic performance could be attributed to electron-deficient Rh species,which reduced CO adsorption while simultaneously promoting alkene adsorption through increased EMSIs.These findings suggest that tuning EMSIs is an effective way to achieve SACs with high activity and durability.展开更多
The nitrogen-coordinated metal single-atom catalysts(M−N−C SACs)with an ultra-high metal loading synthetized by direct high-temperature pyrolysis have been widely reported.However,most of metal single atoms in these c...The nitrogen-coordinated metal single-atom catalysts(M−N−C SACs)with an ultra-high metal loading synthetized by direct high-temperature pyrolysis have been widely reported.However,most of metal single atoms in these catalysts were buried in the carbon matrix,resulting in a low metal utilization and inaccessibility for adsorption of reactants during the catalytic process.Herein,we reported a facile synthesis based on the hard-soft acid-base(HSAB)theory to fabricate Co single-atom catalysts with highly exposed metal atoms ligated to the external pyridinic-N sites of a nitrogen-doped carbon support.Benefiting from the highly accessible Co active sites,the prepared Co−N−C SAC exhibited a superior oxygen reduction reactivity comparable to that of the commercial Pt/C catalyst,showing a high turnover frequency(TOF)of 0.93 e^(−)·s^(-1)·site^(-1)at 0.85 V vs.RHE,far exceeding those of some representative SACs with a ultra-high metal content.This work provides a rational strategy to design and prepare M−N−C single-atom catalysts featured with high site-accessibility and site-density.展开更多
Single-atom catalysts(SACs)hold significant importance in catalysis due to their maximized atomic utilization efficiency,well-tuned active sites,and exceptional catalytic activity.However,their practical applications ...Single-atom catalysts(SACs)hold significant importance in catalysis due to their maximized atomic utilization efficiency,well-tuned active sites,and exceptional catalytic activity.However,their practical applications are hindered by the high cost of precursor materials and the complexity of sustainable synthesis.Biomass with diverse dimensions and chemical components has of potential to serve as a carbon substrate for the synthesis of high-performance SACs,which helps to promote the sustainable development for energy conversion,improve energy efficiency,and reduce environmental pollution.This review systematically introduces the synthesis methods,structure characterization techniques,and structure regulation strategies of biomass-based SACs(Bio-SACs).The recent advancements in Bio-SACs for energy conversion applications,including electrocatalysis,thermal catalysis,and photocatalysis,have been summarized.The challenges in the practical applications of Bio-SACs and the future research directions are highlighted with an emphasis on the impact of artificial intelligence(AI)and machine learning(ML)technologies in the design and fabrication of high-performance Bio-SACs.展开更多
Precisely tailoring metal single-atoms within zeolite scaffolds and understanding the origin of the unique behavior of such atomically dispersed catalysts are pivotal and challenge in chemistry and catalysis.Herein,we...Precisely tailoring metal single-atoms within zeolite scaffolds and understanding the origin of the unique behavior of such atomically dispersed catalysts are pivotal and challenge in chemistry and catalysis.Herein,we have successfully fabricated Ni single-atoms within BEA zeolite(Ni_(1)@Beta)through a facile in situ two-step hydrothermal strategy,notably without using any chelating agent for stabilizing Ni species.With the aid of advanced characterization techniques,such as aberration-corrected high-angle annular dark-field scanning transmission electron microscopy,X-ray absorption spectroscopy,etc.,and combined with density functional theory calculations,the nature and micro-environment of isolated Ni species,which are incorporated within 6-membered rings and stabilized by four skeletal oxygens of Beta zeolite,have been identified.The as-obtained Ni1@Beta exhibits a superior performance in terms of activity(with a turnover frequency value up to 114.1 h^(-1))and stability(for 5 consecutive runs)in the selective hydrogenation of furfural,surpassing those of Ni nanoparticle analogues and previously reported Ni-based heterogeneous catalysts.This study provides an efficient strategy for the fabrication of non-noble metal single-atoms within zeolites,which could be of great help for the design of metal-zeolite combinations in the chemoselective reactions involved in biomass conversion and beyond.展开更多
The co-production of hydrogen and value-added biochemicals from lignocellulose utilizing solar energy has been regarded as one of the technologies most potentially able to alleviate the current energy crisis.Here,we d...The co-production of hydrogen and value-added biochemicals from lignocellulose utilizing solar energy has been regarded as one of the technologies most potentially able to alleviate the current energy crisis.Here,we demonstrate a cost-effective photoreforming strategy for lignocellulose valorization using a carbon nitride-supported platinum single-atom photocatalyst.An advanced H_(2) evolution rate of 6.34 mmol molPt^(-1) h^(-1) is achieved over the optimal catalyst,which is around 4.6 and 30.5 times higher compared with the nanosized Pt counterpart and pristine carbon nitride,respectively.Meanwhile,the monosaccharides are oxidized to value-added lactic acid with>99%conversion and extraordinary selectivity up to 97%.The theoretical calculations show that with Pt incorporation,the photogenerated holes are predominantly localized on the metal sites while the photogenerated electrons are concentrated on C_(3)N_(4),thus enhancing the effective separation of charge carriers.This work provides a promising avenue for the simultaneous production of green H2 and bio-based chemicals by biomass photorefinery.展开更多
With the rapid advancement of portable energy devices and sensor technologies,enhancing their catalytic performance,sensing capabilities,and application reliability has become a critical challenge in the fields of mat...With the rapid advancement of portable energy devices and sensor technologies,enhancing their catalytic performance,sensing capabilities,and application reliability has become a critical challenge in the fields of materials and energy science.Single-atom catalysts(SACs),owing to their high atomic utilization,outstanding catalytic activity,and precisely engineered structures enabled by density functional theory and enhanced by artificial intelligence,have shown tremendous potential in advancing portable energy and sensing technologies.While existing reviews predominantly focus on the application of SACs in individual portable devices,systematic discussions on their overall development prospects and challenges within portable energy and sensor fields remain scarce.Therefore,this review comprehensively explores the application potential and recent advancements of SACs in portable zinc-air batteries,proton exchange membrane fuel cells,and sensor technologies.The article highlights the influence of key factors such as material design,structural optimization,and packaging integration on device performance,while also addressing the primary bottlenecks and challenges encountered in current practical applications.Furthermore,it suggests possible future development directions,aiming to offer theoretical insights and engineering guidance for the large-scale deployment of SACs in wearable electronic devices,portable energy systems,and smart sensing technologies.展开更多
Metal oxides as support for constructing precious metal single-atom catalysts hold great promise for a wide range of industrial applications,but achieving a high-loading of thermally stable metal single atoms on such ...Metal oxides as support for constructing precious metal single-atom catalysts hold great promise for a wide range of industrial applications,but achieving a high-loading of thermally stable metal single atoms on such supports has been challenging.Herein,we report an innovative strategy for the fabrication of high-density single-atoms(Rh,Ru,Pd)catalysts on CaAl-layered double hydroxides(CaAl-LDH)via isomorphous substitution.The Rh species have occupied Ca^(2+)vacancies within CaAl-LDH laminate by ion-exchange,facilitating a substantial loading of isolated Rh single-atoms.Such catalysts displayed superior performance in the selective hydrogenation to quinoline,pivotal for liquid organic hydrogen storage,and the universality for the hydrogenation of N-heterocyclic aromatic hydrocarbons was also verified.Combining the experimental results and density functional theory calculations,the pathway of quinoline hydrogenation over Rh1CaAl-LDH was proposed.This synthetic strategy marks a significant advancement in the field of single-atom catalysts,expanding their horizons in green chemical processes.展开更多
Hydroisomerization of n-alkanes plays an important role in fuel and lubricants processing.Bifunctional catalysts with ultralow platinum loading have recently been reported successively for hydroisomerisation.Herein,th...Hydroisomerization of n-alkanes plays an important role in fuel and lubricants processing.Bifunctional catalysts with ultralow platinum loading have recently been reported successively for hydroisomerisation.Herein,the catalysts were prepared successfully with different methods to improve the catalytic performance.The conversion of 0.01%Pt1@CeOx/SAPO-11 prepared by co-calcination method(0.01%Pt1@CS-c)is 71.4%,25%higher than the other prepared by precipitation method.The turnover frequency per active surface platinum site(TOFPt)of 0.01%Ptl@CS-c is as high as 13115 h^(-1).Revealed by the X-ray photoelectron spectroscopy(XPS)results,the quality of phase boundary/intersurface between ceria and zeolite is found significantly different.The conjunction quality of phase boundary directly affects the spillover rate of intermediate species,which further leads to an apparent activity difference.In addition,the possible role of ceria in the reaction is discussed,rather than just as a carrier for the active metal atoms.展开更多
Hydrogen is a highly promising energy carrier because of its renewable and clean qualities.Among the different methods for H_(2) production,photoelectrocatalysis(PEC)water splitting has garnered significant interest,t...Hydrogen is a highly promising energy carrier because of its renewable and clean qualities.Among the different methods for H_(2) production,photoelectrocatalysis(PEC)water splitting has garnered significant interest,thanks to the abundant and perennial solar energy.Single-atom catalysts(SACs),which feature well-distributed atoms anchored on supports,have gained great attention in PEC water splitting for their unique advantages in overcoming the limitations of conventional PEC reactions.Herein,we comprehensively review SAC-incorporated photoelectrocatalysts for efficient PEC water splitting.We begin by highlighting the benefits of SACs in improving charge transfer,catalytic selectivity,and catalytic activity,which address the limitations of conventional PEC reactions.Next,we provide a comprehensive overview of established synthetic techniques for optimizing the properties of SACs,along with modern characterization methods to confirm their unique structures.Finally,we discuss the challenges and future directions in basic research and advancements,providing insights and guidance for this developing field.展开更多
Propane dehydrogenation(PDH)has emerged as a key on-purpose technology for the production of propylene,but it often depends on toxic chromium and expensive platinum catalysts,highlighting the need for environmentally ...Propane dehydrogenation(PDH)has emerged as a key on-purpose technology for the production of propylene,but it often depends on toxic chromium and expensive platinum catalysts,highlighting the need for environmentally friendly and cost-effective alternatives.In this study,we developed a facile impregnation method to fabricate unsaturated Co single-atoms with a tricoordinated Co_(1)O_(3)H_(x) structure by regulating silanol nests in purely siliceous Beta zeolites.Detailed PDH catalytic tests and characterizations revealed a positive correlation between the presence of silanol nests and enhanced catalytic activity.Additionally,the unsaturated Co single-atoms exhibited a carbon deposition rate more than an order of magnitude slower than that of Co nanoparticles.Notably,the optimized Co_(0.3%)/deAl-meso-Beta catalyst achieved a record-high propylene formation rate of 21.2 mmol_(C3H6) g_(cat)^(-1) h^(-1),with an exceptional propylene selectivity of 99.1%at 550℃.Moreover,the Co_(0.3%)/deAl-meso-Beta catalyst demonstrated excellent stability,with negligible deactivation after 5 consecutive regeneration cycles.This study emphasizes the pivotal role of silanol nests of zeolites in stabilizing and modulating the coordination environment of metallic active sites,providing valuable insights for the design of high-activity,high-stability,and low-cost PDH catalysts.展开更多
Enhancing the corrosion resistance of carriers within Fenton-like systems and inhibiting the migration and aggregation of single atoms in reaction environments are essential for maintaining both high activity and stab...Enhancing the corrosion resistance of carriers within Fenton-like systems and inhibiting the migration and aggregation of single atoms in reaction environments are essential for maintaining both high activity and stability at catalytic sites,thus meeting fundamental requirements for practical application.The Fenton-like process of activating various strong oxidants by silicon-based single atom catalysts(SACs)prepared based on silicon-based materials(mesoporous silica,silicon-based minerals,and organosilicon materials)has unique advantages such as structural stability(especially important under strong oxidation conditions)and environmental protection.In this paper,the preparation strategies for the silicon-based SACs were assessed first,and the structural characteristics of various silicon-based SACs are systematically discussed,their application process and mechanism in Fenton-like process to achieve water purification are investigated,and the progress of Fenton-like process in density functional theory(DFT)of siliconbased derived single atom catalysts is summarized.In this paper,the preparation strategies and applications of silicon-based derived SACs are analyzed in depth,and their oxidation activities and pathways to different pollutants in water are reviewed.In addition,this paper also summarizes the device design and application of silicon-based derived SACs,and prospects the future development of silicon-based SACs in Fenton-like applications.展开更多
文摘The sluggish kinetics of the oxygen reduction reaction(ORR)and high over potential of oxygen evolution reaction(OER)are big challenges in the development of high-performance zinc-air batteries(ZABs)and fuel cells.In this work,we report a rational design and a simple fabrication strategy of a photo-enhanced Co single-atom catalyst(SAC)comprising g-C3N4 coupled with cobalt-nitrogen-doped hierarchical mesoporous carbon(Co-N/MPC),forming a staggered p-n heterojunction that effectively improves charge separation and enhances electrocatalytic activity.The incorporation of Co SACs and g-C3N4 synergistically optimizes the photogenerated electron-hole pair separation,significantly boosting the intrinsic ORR-OER duplex activity.Under illumination,g-C_(3)N_(4)@Co-N/MPC exhibits an outstanding ORR half-wave potential(E1/2)of 0.841 V(vs.RHE)in 0.1 mol L^(–1)KOH and a low OER overpotential of 497.4 mV(vs.RHE)at 10 mA cm^(–2)in 1 mol L^(–1)KOH.Notably,the catalyst achieves an exceptional peak power density of 850.7 mW cm^(–2)in ZABs and of 411 mW cm^(–2)even in H_(2)-air fuel cell.In addition,g-C_(3)N_(4)@Co-N/MPC-based ZABs also show remarkable cycling stability exceeding 250 h.The advanced photo-induced charge separation at the p-n heterojunction facilitates faster electron transfer kinetics,and the mass transport owing to hierarchical mesoporous structure of Co-N-C,thereby reducing the overpotential and enhancing the overall energy conversion efficiency.This work provides a new perspective on designing next-generation of single-atom dispersed oxygen reaction catalysts,paving the way for high-performance photo-enhanced energy storage and conversion systems.
文摘Synthesis of primary amines from alcohols is an economical and green route to access high-value N-compounds.However,challenges remain to develop both cost-effective and efficient catalysts.In this study,we developed a Ru-Co/ZrO_(2)single-atom alloy catalyst which afforded diverse primary amines from alcohols in the presence of ammonia and hydrogen with exceptional conversion(up to 90%)and selectivity(80%)under mild conditions(0.7 MPa NH_(3),0.3 MPa H_(2),160℃)and exhibited satisfactory stability upon regeneration.The turnover rate was approximately 8.4 times higher than that observed over the Co/ZrO_(2)catalyst.Characterizations indicated that the alloyed Ru facilitated the reduction of Co,strengthened the interaction with H_(2)and mitigated the over-strong adsorption of aldehyde intermediates.These combined effects contributed significantly to the enhanced catalytic performances.This work presents a promising strategy for the development of advanced catalysts in the amination of alcohols.
基金This work was supported by the KIST Institutional Program(2E32461)the NationalResearch Council of Science&Technology(NST)grant(CPS21041-100)+1 种基金the National Research Foundation ofKorea(NRF)grant funded by the Korea Government(MSIT)(No.RS-2023-00209940,NRF-2022R 1F1A1068725, NRF-2022M3H4A7046278)Korea EnvironmentIndustry&Technology Institute(KEITI)through theEcological Imitation-based Environmental Pollution Man-agement Technology Development Project,funded by theKorea Ministry of Environment(MOE)(2021002800005).
文摘Atomically dispersed single-atom catalysts(SACs)on carbon supports show great promise for H_(2)O_(2) electrosynthesis,but conventional wet chemistry methods using particulate carbon blacks in powder form have limited their potential as two-electron(2^(e−))oxygen reduction reaction(ORR)catalysts.Here,we demonstrate high-performance Co SACs supported on a free-standing aligned carbon nanofiber(CNF)using electrospinning and arc plasma deposition(APD).Based on the surface oxidation treatment of aligned CNF and precise control of the deposition amount in a dry-based APD process,we successfully form densely populated Co SACs on aligned CNF.Through experimental analyses and density functional theory calculations,we reveal that Co SAC has a Co–N_(2)–O_(2) moiety with one epoxy group,leading to excellent 2^(e−)ORR activity.Furthermore,the aligned CNF significantly improves mass transfer in flow cells compared to randomly oriented CNF,showing an overpotential reduction of 30 mV and a 1.3-fold improvement(84.5%)in Faradaic efficiency,and finally achieves an outstanding production rate of 15.75 mol gcat^(−1) h^(−1) at 300 mA cm^(−2).The high-performance Co SAC supported on well-aligned CNF is also applied in an electro-Fenton process,demonstrating rapid removal of methylene blue and bisphenol F due to its exceptional 2e^(−)ORR activity.
基金financially supported by Talent Start-up Fund of Fuzhou University(No.0180-511208)Fuzhou University Testing Fund of precious apparatus(No.2023T002)+1 种基金the National Natural Science Foundation of China(Nos.21703038 and 22072025)The financial support from State Key Laboratory of Structural Chemistry,Fujian Institute of Research on the Structure of Matter,Chinese Academy of Sciences is acknowledged(No.20240018).
文摘Single-atom catalysts(SACs)have garnered tremendous and continuous attention in photocatalytic CO_(2)reduction reactions(CO_(2)RR),due to their compelling potential in broadening the light-harvesting range,elevating the charge separation/transfer efficiency,and enhancing surface reaction.Despite the surge in research and the expanding range of potential central metal candidates—including d-block,p-block,and rare metal elements,etc.—the comprehension of the structure-function relationships between the central metal and its performance remains elusive.Hence,categorized by different areas of the central metal element from periodic table,we outline the recent progress and challenges on SACs for photocatalytic CO_(2)RR.We begin by describing various synthetic strategies employed for SACs.Subsequently,a clear classification of the SACs applications in photocatalytic CO_(2)RR is provided,according to the central metal elements in different blocks of the periodic table.We also discussed how isolated metal single-atom sites from different blocks of the periodic table improve the performance of photocatalytic CO_(2)reduction from the perspective of charge separation and transfer.Finally,we end this review with some perspectives and challenges associated with SACs for photocatalytic CO_(2)reduction.Through this review,we aim to enrich the element diversity of SACs for photocatalytic CO_(2)RR,reveal trends in element evolution,and propose directions for future development in this flourishing field.
基金the National Natural Science Foundation of China(No.22379069)Fundamental Research Funds for the Central Universities(No.30922010304).
文摘Sluggish sulfur redox kinetics remain a critical bottleneck in the advancement of high-performance lithiumsulfur batteries(LSBs).Single-atom catalysts(SACs)offer a promising solution to this limitation,particularly when their coordination structures are carefully engineered.Here,we develop a chromium-based SAC featuring a unique undercoordinated CrN_(3) configuration to boost sulfur electrochemistry.Compared with conventional CrN_(4),the CrN_(3) motif lowers 3d orbital occupancy and meanwhile activates the in-plane hybridizations with S 3p orbitals upon interaction with polysulfides,contributing to moderate adsorption strength and reduced energy barriers for bidirectional sulfur conversions.Additionally,the integration of the two-dimensional(2D)porous framework ensures abundant electrochemically active surfaces and efficiently exposed active sites.As a result,CrN_(3)-based cells demonstrate fast and durable sulfur redox reactions,enabling an ultralow capacity decay of 0.0075%per cycle over 1000 cycles and a high-rate capability of 651.9 mAh·g^(-1)at 5 C.The CrN_(3) catalyst retains robust catalytic efficiency under demanding conditions,delivering a high areal capacity of 5.53 mAh·cm^(-2) at high sulfur loading and lean electrolyte.This work establishes a compelling paradigm of SAC coordination engineering for designing advanced sulfur electrocatalysts for next-generation LSBs.
基金supported financially by the National Natural Science Foundation of China(No.52172208)Taishan Scholar Young Talent Program(No.tsqn202306216)Shandong Excellent Young Scientists Fund Program(Overseas,2023HWYQ‑091).
文摘Oxygen reduction reaction(ORR)is crucial for Znair batteries,while also serves as a core electrochemical process in oxygen depolarized cathodes(ODCs)for chlor-alkali electrolysis.The lack of cost-effective,highly active ORR electrocatalysts with superior kinetics hinders progress in this field.Herein,we report the Fe/Ni dual single-atomic sites anchored by commercial carbon black(Fe/Ni-N/CB)using rigid ligand confined and high-temperature shock(HTS)strategy in less than 0.5 s.Theoretical calculation reveals that singleatomic Fe is the real active site.Single-atomic Fe and Ni species in Fe/Ni-N/CB synergistically accelerate the kinetics of ORR by reducing the energy barrier of the rate-determining step.A large half-wave potential(E_(1/2))of 0.907 V is achieved in 0.1 M KOH aqueous solution.The assembled aqueous Zn-air battery(A-ZAB)with Fe/Ni-N/CB cathode presents remarkable charge-discharge cycling stability for over 650 h without voltage gap degradation.The quasi-solid-state Zn-air battery(QSS-ZAB)exhibits excellent reversibility over a 150-h operation at 0.5 mA·cm^(-2) with negligible energy conversion efficiency recession.Impressively,Fe/Ni-N/CB||RuO_(2)chloralkali flow cell exhibits a low cell voltage of 1.60 V at a large current density of 300 mA·cm^(-2) at 80℃,and demonstrates exceptional durability with 7% current density decay over 150 h of continuous operation at 100 mA·cm^(-2).Fe/Ni-N/CB||RuO_(2)achieves near-ideal caustic current efficiency(~97.2%)at the current density of 300 mA·cm^(-2).This work provides a rapid and economical synthesis technique for the synthesis of catalysts at the atomic scale while demonstrating significant potential for application in energy-saving chlor-alkali electrolyzer.
基金funded by the National Natural Science Foundation of China(Nos.52176104 and 52006073)the Natural Science Foundation of Hebei Province(No.B2023502023)Fundamental Research Fund for the Central Universities(Nos.2023MS125 and 2024MS154).
文摘NO oxidation with H_(2)O_(2)as the oxidant is a promising green denitration technology.However,the current metal oxide catalysts still have many disadvantages for this reaction,such as insufficient catalytic activity for H_(2)O_(2)activation,poor selectivity,and low stability.In this study,we employ atomically dispersed Co anchored on SBA-15 with Co-O_(4)structure for NO oxidation,which achieves a 90%removal efficiency of NO under low molar ratio of H_(2)O_(2)to NO(1.56),ultra-low temperature(80℃),and ultra-high space velocity(720,000 h^(-1)),representing the top-level performance among previously reported catalysts.More interestingly,our work reveals that by taking advantage of the uniform Co-O_(4)structure,H_(2)O_(2)is mainly directionally converted into·O_(2)^(-)at the Co-O_(4)site,and·O_(2)^(-)plays a key role for achieving the deep-oxidation of NO to produce NO_(3)^(-),which is contrast to the previously reports that^(1)O_(2)is the main free radical for NO oxidation.This study highlights the great potentials of single-atom catalysts for improving the H_(2)O_(2)utilization performance for NO oxidation.
文摘Solving the problems of carbon dioxide(CO_(2))emissions and energy scarcity by the development of highly selective,cost-effective,and reliable catalysts for the electrochemical reduction of CO_(2)to useful carbon-based products would be very helpful.We report the synthesis of an efficient graphene-supported bismuth single-atom catalyst(BiSA-G)featuring a BiN_(4)coordination structure for this purpose.The synthesis used tannic acid as a multifunctional ligand and ammonia as a nitrogen dopant.Using a scalable coordination chemistry approach,BiN_(4)sites were uniformly dispersed on the graphene substrate and were found to have an outstanding ability for the conversion of CO_(2)to CO,with a high Faradaic efficiency of 97.4%at−0.55 V(vs.RHE)and a high turnover frequency of 5230 h^(−1)along with outstanding stability.Density functional theory calculations confirmed that the BiN_(4)site serves as the dominant active center,simultaneously facilitating CO_(2)activation and the efficient formation of the crucial intermediate*COOH with a reduced free energy barrier.This discovery offers a new way for the atomic-scale design of high-efficiency catalysts for the electrochemical CO_(2)reduction reaction,potentially helping sustainable carbon use.
文摘In recent years,numer-ous single-atom catalysts(SACs)have been synthesized to activate persulfate(PS)by a non-radical pathway because of its high se-lectivity,and activity for the cata-lyst.Metal-nitrogen-carbon(M-N_(x)-C)has been identified as the key active site in SACs.Although methods for preparing SACs have been extensively reported,a systematic summary of the direct construction of M-N_(x)-C,espe-cially unconventional metal-nitrogen-carbon(UM-N_(x)-C,x≠4),on SACs for PS non-radical activation has still not been reported.The role of the M-N_(x)-C active sites on PS non-radical activation is discussed and methods for the formation of M-N_(x)-C and UM-N_(x)-C active sites in SACs and the effect of catalyst carriers such as carbon nitride(g-C_(3)N_(4)),MOFs,COFs,and other car-bon materials are reviewed.Direct and indirect methods,especially for UM-N_(x)-C active site formation,are also elaborated.Factors affecting the formation of a M-N_(x)-C active site on SACs are also discussed.Prospects for the use of M-N_(x)-C active sites for the non-radical activation of PS by SACs to remove organic contaminants from wastewater are evaluated.
基金supported by the Petrochemical Research Institute Foundation(21-CB-09-01)the National Natural Science Foundation of China(22302186,22025205)+1 种基金the China Postdoctoral Science Foundation(2022M713030,2023T160618)the Fundamental Research Funds for the Central Universities(WK2060000058,WK2060000038).
文摘By simplifying catalyst-product separation and reducing phosphorus waste,heterogeneous hydroformylation offers a more sustainable alternative to homogeneous processes.However,heterogeneous hydroformylation catalysts developed thus far still suffer from the issues of much lower activity and metal leaching,which severely hinder their practical application.Here,we demonstrate that incorporating phosphorus(P)atoms into graphitic carbon nitride(PCN)supports facilitates charge transfer from Rh to the PCN support,thus largely enhancing electronic metal-support interactions(EMSIs).In the styrene hydroformylation reaction,the activity of Rh_(1)/PCN single-atom catalysts(SACs)with varying P contents exhibited a volcano-shaped relationship with P doping,where the Rh_(1)/PCN SAC with optimal P doping showed exceptional activity,approximately 5.8-and 3.3-fold greater than that of the Rh_(1)/g-C_(3)N_(4)SAC without P doping and the industrial homogeneous catalyst HRh(CO)(PPh_(3))_(3),respectively.In addition,the optimal Rh_(1)/PCN SAC catalyst also demonstrated largely enhanced multicycle stability without any visible metal aggregation owing to the increased EMSIs,which sharply differed from the severe metal aggregation of large nanoparticles on the Rh_(1)/g-C_(3)N_(4)SAC.Mechan-istic studies revealed that the enhanced catalytic performance could be attributed to electron-deficient Rh species,which reduced CO adsorption while simultaneously promoting alkene adsorption through increased EMSIs.These findings suggest that tuning EMSIs is an effective way to achieve SACs with high activity and durability.
基金supported by Shanxi Province Science Foundation for Youths(202203021212300)Taiyuan University of Science and Technology Scientific Research Initial Funding(20212064)Outstanding Doctoral Award Fund in Shanxi Province(20222060).
文摘The nitrogen-coordinated metal single-atom catalysts(M−N−C SACs)with an ultra-high metal loading synthetized by direct high-temperature pyrolysis have been widely reported.However,most of metal single atoms in these catalysts were buried in the carbon matrix,resulting in a low metal utilization and inaccessibility for adsorption of reactants during the catalytic process.Herein,we reported a facile synthesis based on the hard-soft acid-base(HSAB)theory to fabricate Co single-atom catalysts with highly exposed metal atoms ligated to the external pyridinic-N sites of a nitrogen-doped carbon support.Benefiting from the highly accessible Co active sites,the prepared Co−N−C SAC exhibited a superior oxygen reduction reactivity comparable to that of the commercial Pt/C catalyst,showing a high turnover frequency(TOF)of 0.93 e^(−)·s^(-1)·site^(-1)at 0.85 V vs.RHE,far exceeding those of some representative SACs with a ultra-high metal content.This work provides a rational strategy to design and prepare M−N−C single-atom catalysts featured with high site-accessibility and site-density.
基金supported by the National Natural Science Foundation of China(No.51502108)the Jilin University Concept Validation Project of Scientific and Technological Achievements(No.2024GN010)the Jilin University Funding Project of Graduate Education Teaching Reform and Research(No.2025GCSY19).
文摘Single-atom catalysts(SACs)hold significant importance in catalysis due to their maximized atomic utilization efficiency,well-tuned active sites,and exceptional catalytic activity.However,their practical applications are hindered by the high cost of precursor materials and the complexity of sustainable synthesis.Biomass with diverse dimensions and chemical components has of potential to serve as a carbon substrate for the synthesis of high-performance SACs,which helps to promote the sustainable development for energy conversion,improve energy efficiency,and reduce environmental pollution.This review systematically introduces the synthesis methods,structure characterization techniques,and structure regulation strategies of biomass-based SACs(Bio-SACs).The recent advancements in Bio-SACs for energy conversion applications,including electrocatalysis,thermal catalysis,and photocatalysis,have been summarized.The challenges in the practical applications of Bio-SACs and the future research directions are highlighted with an emphasis on the impact of artificial intelligence(AI)and machine learning(ML)technologies in the design and fabrication of high-performance Bio-SACs.
文摘Precisely tailoring metal single-atoms within zeolite scaffolds and understanding the origin of the unique behavior of such atomically dispersed catalysts are pivotal and challenge in chemistry and catalysis.Herein,we have successfully fabricated Ni single-atoms within BEA zeolite(Ni_(1)@Beta)through a facile in situ two-step hydrothermal strategy,notably without using any chelating agent for stabilizing Ni species.With the aid of advanced characterization techniques,such as aberration-corrected high-angle annular dark-field scanning transmission electron microscopy,X-ray absorption spectroscopy,etc.,and combined with density functional theory calculations,the nature and micro-environment of isolated Ni species,which are incorporated within 6-membered rings and stabilized by four skeletal oxygens of Beta zeolite,have been identified.The as-obtained Ni1@Beta exhibits a superior performance in terms of activity(with a turnover frequency value up to 114.1 h^(-1))and stability(for 5 consecutive runs)in the selective hydrogenation of furfural,surpassing those of Ni nanoparticle analogues and previously reported Ni-based heterogeneous catalysts.This study provides an efficient strategy for the fabrication of non-noble metal single-atoms within zeolites,which could be of great help for the design of metal-zeolite combinations in the chemoselective reactions involved in biomass conversion and beyond.
文摘The co-production of hydrogen and value-added biochemicals from lignocellulose utilizing solar energy has been regarded as one of the technologies most potentially able to alleviate the current energy crisis.Here,we demonstrate a cost-effective photoreforming strategy for lignocellulose valorization using a carbon nitride-supported platinum single-atom photocatalyst.An advanced H_(2) evolution rate of 6.34 mmol molPt^(-1) h^(-1) is achieved over the optimal catalyst,which is around 4.6 and 30.5 times higher compared with the nanosized Pt counterpart and pristine carbon nitride,respectively.Meanwhile,the monosaccharides are oxidized to value-added lactic acid with>99%conversion and extraordinary selectivity up to 97%.The theoretical calculations show that with Pt incorporation,the photogenerated holes are predominantly localized on the metal sites while the photogenerated electrons are concentrated on C_(3)N_(4),thus enhancing the effective separation of charge carriers.This work provides a promising avenue for the simultaneous production of green H2 and bio-based chemicals by biomass photorefinery.
文摘With the rapid advancement of portable energy devices and sensor technologies,enhancing their catalytic performance,sensing capabilities,and application reliability has become a critical challenge in the fields of materials and energy science.Single-atom catalysts(SACs),owing to their high atomic utilization,outstanding catalytic activity,and precisely engineered structures enabled by density functional theory and enhanced by artificial intelligence,have shown tremendous potential in advancing portable energy and sensing technologies.While existing reviews predominantly focus on the application of SACs in individual portable devices,systematic discussions on their overall development prospects and challenges within portable energy and sensor fields remain scarce.Therefore,this review comprehensively explores the application potential and recent advancements of SACs in portable zinc-air batteries,proton exchange membrane fuel cells,and sensor technologies.The article highlights the influence of key factors such as material design,structural optimization,and packaging integration on device performance,while also addressing the primary bottlenecks and challenges encountered in current practical applications.Furthermore,it suggests possible future development directions,aiming to offer theoretical insights and engineering guidance for the large-scale deployment of SACs in wearable electronic devices,portable energy systems,and smart sensing technologies.
文摘Metal oxides as support for constructing precious metal single-atom catalysts hold great promise for a wide range of industrial applications,but achieving a high-loading of thermally stable metal single atoms on such supports has been challenging.Herein,we report an innovative strategy for the fabrication of high-density single-atoms(Rh,Ru,Pd)catalysts on CaAl-layered double hydroxides(CaAl-LDH)via isomorphous substitution.The Rh species have occupied Ca^(2+)vacancies within CaAl-LDH laminate by ion-exchange,facilitating a substantial loading of isolated Rh single-atoms.Such catalysts displayed superior performance in the selective hydrogenation to quinoline,pivotal for liquid organic hydrogen storage,and the universality for the hydrogenation of N-heterocyclic aromatic hydrocarbons was also verified.Combining the experimental results and density functional theory calculations,the pathway of quinoline hydrogenation over Rh1CaAl-LDH was proposed.This synthetic strategy marks a significant advancement in the field of single-atom catalysts,expanding their horizons in green chemical processes.
基金Project supported by National Natural Science Foundation of China(22078159,U19B2001)。
文摘Hydroisomerization of n-alkanes plays an important role in fuel and lubricants processing.Bifunctional catalysts with ultralow platinum loading have recently been reported successively for hydroisomerisation.Herein,the catalysts were prepared successfully with different methods to improve the catalytic performance.The conversion of 0.01%Pt1@CeOx/SAPO-11 prepared by co-calcination method(0.01%Pt1@CS-c)is 71.4%,25%higher than the other prepared by precipitation method.The turnover frequency per active surface platinum site(TOFPt)of 0.01%Ptl@CS-c is as high as 13115 h^(-1).Revealed by the X-ray photoelectron spectroscopy(XPS)results,the quality of phase boundary/intersurface between ceria and zeolite is found significantly different.The conjunction quality of phase boundary directly affects the spillover rate of intermediate species,which further leads to an apparent activity difference.In addition,the possible role of ceria in the reaction is discussed,rather than just as a carrier for the active metal atoms.
基金supported by the National Natural Science Foundation of China(Nos.22209186,22479149)Self-deployed Projects of Ganjiang Innovation Academy,CAS(No.E355F006)+2 种基金Natural Science Foundation of Jiangxi Province(No.20242BAB23016)Key Research and Development Program of Jiangxi Province(Nos.20223BBG74004,20232BBG70003)Youth Innovation Promotion Association,Chinese Academy of Sciences(No.2023343).
文摘Hydrogen is a highly promising energy carrier because of its renewable and clean qualities.Among the different methods for H_(2) production,photoelectrocatalysis(PEC)water splitting has garnered significant interest,thanks to the abundant and perennial solar energy.Single-atom catalysts(SACs),which feature well-distributed atoms anchored on supports,have gained great attention in PEC water splitting for their unique advantages in overcoming the limitations of conventional PEC reactions.Herein,we comprehensively review SAC-incorporated photoelectrocatalysts for efficient PEC water splitting.We begin by highlighting the benefits of SACs in improving charge transfer,catalytic selectivity,and catalytic activity,which address the limitations of conventional PEC reactions.Next,we provide a comprehensive overview of established synthetic techniques for optimizing the properties of SACs,along with modern characterization methods to confirm their unique structures.Finally,we discuss the challenges and future directions in basic research and advancements,providing insights and guidance for this developing field.
文摘Propane dehydrogenation(PDH)has emerged as a key on-purpose technology for the production of propylene,but it often depends on toxic chromium and expensive platinum catalysts,highlighting the need for environmentally friendly and cost-effective alternatives.In this study,we developed a facile impregnation method to fabricate unsaturated Co single-atoms with a tricoordinated Co_(1)O_(3)H_(x) structure by regulating silanol nests in purely siliceous Beta zeolites.Detailed PDH catalytic tests and characterizations revealed a positive correlation between the presence of silanol nests and enhanced catalytic activity.Additionally,the unsaturated Co single-atoms exhibited a carbon deposition rate more than an order of magnitude slower than that of Co nanoparticles.Notably,the optimized Co_(0.3%)/deAl-meso-Beta catalyst achieved a record-high propylene formation rate of 21.2 mmol_(C3H6) g_(cat)^(-1) h^(-1),with an exceptional propylene selectivity of 99.1%at 550℃.Moreover,the Co_(0.3%)/deAl-meso-Beta catalyst demonstrated excellent stability,with negligible deactivation after 5 consecutive regeneration cycles.This study emphasizes the pivotal role of silanol nests of zeolites in stabilizing and modulating the coordination environment of metallic active sites,providing valuable insights for the design of high-activity,high-stability,and low-cost PDH catalysts.
基金supported by National Natural Science Foundation of China(No.52170086)Natural Science Foundation of Shandong Province(No.ZR2021ME013)+1 种基金Natural science Foundation of Shaanxi province(No.2024JC-YBQN-0252)Special Scientific Research Project of Hanzhong City-Shaanxi University of Technology Co-construction State Key Laboratory(No.SXJ2106)。
文摘Enhancing the corrosion resistance of carriers within Fenton-like systems and inhibiting the migration and aggregation of single atoms in reaction environments are essential for maintaining both high activity and stability at catalytic sites,thus meeting fundamental requirements for practical application.The Fenton-like process of activating various strong oxidants by silicon-based single atom catalysts(SACs)prepared based on silicon-based materials(mesoporous silica,silicon-based minerals,and organosilicon materials)has unique advantages such as structural stability(especially important under strong oxidation conditions)and environmental protection.In this paper,the preparation strategies for the silicon-based SACs were assessed first,and the structural characteristics of various silicon-based SACs are systematically discussed,their application process and mechanism in Fenton-like process to achieve water purification are investigated,and the progress of Fenton-like process in density functional theory(DFT)of siliconbased derived single atom catalysts is summarized.In this paper,the preparation strategies and applications of silicon-based derived SACs are analyzed in depth,and their oxidation activities and pathways to different pollutants in water are reviewed.In addition,this paper also summarizes the device design and application of silicon-based derived SACs,and prospects the future development of silicon-based SACs in Fenton-like applications.
