摘要：Developing highly active catalysts for photo/electrocatalytic water splitting is an attractive strategy to produce H2 as a renewable energy *** this study,a new nickel boron oxide/graphdiyne(NiBi/GDY)hybrid catalyst was prepared by a facile synthetic *** from the strong electron donating ability of graphdiyne,NiBi/GDY showed an optimized electronic structure containing lower valence nickel atoms and demonstrated improved catalytic *** expected,NiBi/GDY displayed a high photocatalytic H2 evolution rate of 4.54 mmol g^(-1)h^(-1),2.9 and 4.5 times higher than those of NiBi/graphene and NiBi,***/GDY also displayed outstanding electrocatalytic H2 evolution activity in 1.0 M KOH solution,with a current density of 400 mA/cm^(2)at an overpotential of 478.0 mV,which is lower than that of commercial Pt/C(505.3 mV@400 mA/cm^(2)).This work demonstrates that GDY is an ideal support for the development of highly active catalysts for photo/electrocatalytic H2 evolution.

摘要：Narrow spectral response,low charge separation efficiency and slow water oxidation kinetics of TiO_(2)limit its application in photoelectrochemical and photocatalytic water ***,a promising organic/inorganic composite catalyst Ag/PANI/3DOMM‐TiO_(2–x)with a three‐dimensional ordered macro‐and meso‐porous(3DO MM)structure,oxygen vacancy and Ti^(3+)defects,heterojunction formation and noble metal Ag was designed based on the Z‐scheme mechanism and successfully *** Ag/PANI/3DOMM‐TiO_(2–x)ternary catalyst exhibited enhanced hydrogen production activity in both photocatalytic and photoelectrochemical water *** photocatalytic hydrogen production rate is 420.90μmol g^(–1)h^(–1),which are 19.80 times and 2.06 times higher than the commercial P25 and 3DOMM‐TiO_(2),*** the photoelectrochemical tests,the Ag/PANI/3DOMM‐TiO_(2–x)photoelectrode shows enhanced separation and transfer of carriers with a high current density of 1.55 mA cm^(–2)at equilibrium potential of 1.23 V under simulated AM 1.5 G illumination,which is approximately 5 times greater than the 3DOMM‐TiO_(2).The present work has demonstrated the promising potential of organic/inorganic Z‐scheme photocatalyst in driving water splitting for hydrogen production.

摘要：Electrochemical water splitting is regarded as the most promising approach to produce ***,the sluggish electrochemical reactions occurring at the anode and cathode,namely,the oxygen evolution reaction(OER)and the hydrogen evolution reaction(HER),respectively,consume a tremendous amount of energy,seriously hampering its wide ***,single-atom catalysts(SACs)have been proposed to effectively enhance the kinetics of these two *** this minireview,we focus on the recent progress in SACs for OER and HER *** classes of SACs have been reviewed,i.e.,alloy-based SACs,carbon-based SACs and SACs supported on other *** factors affecting the activities of SACs are also highlighted,including the inherent element property,the coordination environment,the geometric structure and the loading amount of metal ***,we summarize the current problems and directions for future development in SACs.

摘要：Li-ion hybrid supercapacitors （Li-HECs） facilitate effective combination of the advantages of supercapacitors and Li-ion batteries （LIBs）. However, challenges remain in designing and preparing suitable anode and cathode materials, which often require tedious and expensive procedures. Herein, we demonstrated that hollow N-doped carbon capsules （HNC） with and without a Fe304 nanoparticle core can respectively function as the anode and the cathode in very-high-performance Li-HECs. The Fe3Oa@NC anode exhibited a high reversible specific capacity exceeding 1530 mA h g^-1 at 100 mA g^-1 and excellent rate capability （45% capacity retention from 0.1 to 5 A g^-1） and cycle stability （〉97% retention after 100 cycles）. Moreover, high rate performance was achieved in a full-cell using the HNC cathode. By combining the respective structural advantages of the components, the hybrid device with Fe3Oa@NC//HN C exhibited a remark- able energy density of 185 W h kg^-1 at a power density of 39 W kg^-1. The hybrid device furnished a battery-inaccessible power density of 28 kW kg^-1 with rapid charging/discharging within 9 s at an energy density of 95 W h kg^-1.

摘要：Over the past several decades,the utilization of fossil fuels is responsible for mainly excessive atmospheric carbon dioxide(CO_(2))[1-3].Increased concentration of CO_(2)contributes to the major portion of the critical issues faced worldwide,such as global warming and drastic changes in ***,it is imperative to develop an alternative technology that is capable of providing an efficient and sustainable pathway to target the neutralization of CO_(2)level in the atmosphere.

摘要：光催化氧还原制备过氧化氢具有节能、环保等优点.然而,低活性以及低选择性的问题限制了其实际应用.基于金属离子耦合电子转移机制,本文通过浸渍-煅烧法合成了原子分散的钪路易斯酸位点修饰的氮化碳,光合成过氧化氢速率高达55μmol h^(-1),是氮化碳的6.2倍.光催化性能的提升归因于原子分散钪路易斯酸位点与·O_(2)^(-)结合,提高了O_(2)的得电子能力,减少了·O_(2)^(-)逆反应的发生,促进了氧还原反应进行.密度泛函理论模拟及Koutecky-Levich分析表明,钪原子的引入减少了O–O键的断裂,提高了合成过氧化氢的选择性.本研究提出了一种路易斯酸单金属位点光催化剂设计新概念,可同时提升催化反应活性及选择性.

摘要：A series of Ru/FeOx catalysts were synthesized for the selective hydrogenation of CO2to *** characterizations of the catalysts through X‐ray diffraction,X‐ray photoelectron spectroscopy,transmission electron microscopy,and temperature‐programmed techniques were performed to directly monitor the surface chemical properties and the catalytic performance to elucidate the reaction *** dispersed Ru species were observed on the surface of FeOx regardless of the initial Ru *** the Ru loading resulted in changes to the Ru coverage over the FeOx surface,which had a significant impact on the interaction between Ru and adsorbed H,and concomitantly,the H2activation capacity via the ability for *** having0.01%of Ru loading exhibited100%selectivity toward CO resulting from the very strong interaction between Ru and adsorbed H,which limits the desorption of the activated H species and hinders over‐reduction of CO to *** increasing the Ru loading of the catalysts to above0.01%resulted in the adsorbed H to be easily dissociated,as a result of a weaker interaction with Ru,which allowed excessive CO reduction to produce *** how to selectively design the catalyst by tuning the initial loading of the active phase has broader implications on the design of supported metal catalysts toward preparing liquid fuels from CO2.?2018,Dalian institute of Chemical Physics,Chinese Academy of Sciences toward preparing liquid fuels from CO2.?2018,Dalian institute of Chemical Physics,Chinese Academy of *** by Elsevier *** rights reserved.

摘要：设计廉价和高效的双功能催化剂应用于CO_(2)还原和O_(2)还原反应(CO_(2)RR和ORR)是实现碳中和的理想选择.因此,本文研制出铌原子分散固定在氮掺杂有序介孔碳(Nb-N-C)上的双功能CO_(2)RR和ORR催化剂用于锌-空气电池(ZAB)自驱动CO_(2)RR.得益于高铌原子利用率和有序介孔结构,Nb-N-C催化剂展现出高达90%的CO法拉第效率,ORR的半波电位活性为0.84 V,ZAB的峰值功率活性为115.6 mW cm-2.此外,采用两个串联的ZABs单元作为自供能CO_(2)RR系统的电源,能够连续将C O_(2)转化为C O.该自供能系统前10小时的C O平均产率为3.75μmol h-1mg-1cat.理论计算表明,铌原子分散固定在氮掺杂的碳上形成Nb–N配位键,从而有效地降低CO_(2)RR的决速中间体*COOH和ORR的决速中间体*O的生成能垒.

摘要：The design of non-noble metal heterogeneous catalyst with superior performance for selective hydrogenation or transfer hydrogenation of nitroarenes to amines is significant but ***,a single-atom Fe supported by nitrogen-doped carbon(Fe_(1)/N-C)catalyst is *** Fe_(1)/N-C sample shows superior performances for the selective hydrogenation and transfer hydrogenation of nitrobenzene to aniline at different *** functional theory(DFT)calculations show that the superior catalytic activity for the selective hydrogenation at lower temperatures could be attributed to the effective activation of the reactant and intermediates by the Fe_(1)/***,the excellent performance of Fe_(1)/N-C for the selective transfer hydrogenation could be attributed to that the reaction energy barrier for dehydrogenation of isopropanol can be overcome by elevated temperatures.

摘要：氢能作为一种清洁能源,已成为全球能源战略的重要组成部分,也是实现全球“碳中和”的必要途径之一.在可再生电力的驱动下,水电解法有望成为实现“零碳”排放的一种理想的长期制氢方法.与传统合金相比,高熵合金由于其独特的结构特征,包括占位无序和晶格有序,可提供更多的催化活性位点.它们在水解催化剂领域具有广泛的应用前景.本文综述了电解水的机理、水解过程中高熵合金的催化原理,以及高熵合金作为电解水催化剂的最新研究进展.总结了新型高熵合金设计方面存在的难点及其应用潜力,重点讨论了高熵合金在水解催化过程中表面形态和催化活性之间的联系.最后归纳了高熵合金的组成调控及其在水电解等新兴领域的可能应用前景.