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Recent progress of self-supported air electrodes for flexible Zn-air batteries 被引量:1
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作者 Chen Xu Yanli Niu +5 位作者 Vonika Ka-Man Au Shuaiqi Gong Xuan Liu Jianying Wang deli wu Zuofeng Chen 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第2期110-136,I0004,共28页
Smart wearable devices are regarded to be the next prevailing technology product after smartphones and smart homes,and thus there has recently been rapid development in flexible electronic energy storage devices.Among... Smart wearable devices are regarded to be the next prevailing technology product after smartphones and smart homes,and thus there has recently been rapid development in flexible electronic energy storage devices.Among them,flexible solid-state zinc-air batteries have received widespread attention because of their high energy density,good safety,and stability.Efficient bifunctional oxygen electrocatalysts are the primary consideration in the development of flexible solid-state zinc-air batteries,and self-supported air cathodes are strong candidates because of their advantages including simplified fabrication process,reduced interfacial resistance,accelerated electron transfer,and good flexibility.This review outlines the research progress in the design and construction of nanoarray bifunctional oxygen electrocatalysts.Starting from the configuration and basic principles of zinc-air batteries and the strategies for the design of bifunctional oxygen electrocatalysts,a detailed discussion of self-supported air cathodes on carbon and metal substrates and their uses in flexible zinc-air batteries will follow.Finally,the challenges and opportunities in the development of flexible zinc-air batteries will be discussed. 展开更多
关键词 Bifunctional electrocatalysts Oxygen reduction reaction Oxygen evolution reaction Self-supported air electrodes Flexible zinc-air batteries
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通过钨对镍活性位点的电子改性实现苯甲胺选择性氧化耦合制氢
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作者 屠振涛 何晓洋 +5 位作者 刘璇 熊登科 左娟 吴德礼 汪建营 陈作锋 《Chinese Journal of Catalysis》 SCIE CAS CSCD 2024年第3期146-156,共11页
苯甲腈(BN)作为精细化学品、农用化学品和药品生产的重要中间体,其制备受到研究人员的广泛关注.传统的BN化学合成涉及有机物与氰化物之间的亲核取代反应.然而,由于氰化物等剧毒化学试剂的使用,这一反应在实际应用中受到了一定的限制.最... 苯甲腈(BN)作为精细化学品、农用化学品和药品生产的重要中间体,其制备受到研究人员的广泛关注.传统的BN化学合成涉及有机物与氰化物之间的亲核取代反应.然而,由于氰化物等剧毒化学试剂的使用,这一反应在实际应用中受到了一定的限制.最近研究发现,苯甲胺(BA)电化学氧化可为BN的生产提供一种清洁、高效、高选择性的方法.此外,与析氧反应(OER)相比,苯甲胺氧化反应(BAOR)具有明显的热力学优势;将BAOR与阴极析氢反应(HER)耦合,可提高整体电解体系的能效和经济效益.因此,开发高效双功能电催化剂用于苯甲胺氧化及耦合析氢反应具有重要的基础研究意义和实际应用价值.本文通过直接水热和高温磷化的方法,在泡沫镍基底上负载了一种W-Ni_(2)P纳米片(W-Ni_(2)P/NF),并探索了其作为双功能电催化剂在BAOR和HER的应用.实验结果显示,催化剂的纳米片结构不仅提供了充足的活性位点,还有助于离子传输.钨的掺杂显著增强了电化学传导性,改善了水吸附性,并优化了氢吸附能,进而提升了催化剂的HER性能.此外,钨的引入促进了电子从镍向钨的转移,形成了缺电子的镍区域;在W-Ni_(2)P催化的BAOR过程中,缺电子的镍活性位点与供电子的氨基(-NH2)相互作用,有效促进了氨基的吸附和活化,进一步推动了脱氢反应和C≡N键的形成.电化学测试结果表明,在1 mol L^(‒1)KOH溶液中,W-Ni_(2)P催化剂发生HER的过电位为80 mV(10 mA cm^(-2)),其性能可与商业Pt/C电极相媲美.在含有25 mmol L^(‒1)BA的1 mol L^(‒1)KOH溶液中,仅需施加1.42 V电位,W-Ni_(2)P催化剂即可达到100 mA cm^(-2)的氧化电流密度,这比OER所需电位低350 mV.此外,当组装W-Ni_(2)P/NF||W-Ni_(2)P/NF电解槽时,在1 mol L^(‒1)KOH和25 mmol L^(‒1)BA的电解液中,仅需1.41 V的电解电压即可达到10 mA cm^(-2)的电流密度,实现了阴极制氢和阳极增值BN的同时生产,且反应的法拉第效率达到95%.采用电化学原位拉曼光谱和红外光谱研究了反应的活性位点和关键中间产物.结合密度泛函理论计算,阐明了BAOR的催化机理以及反应路径,深入分析了W掺杂在优化吸附能和提高W-Ni2P电催化剂催化活性方面的优化作用.综上所述,本文成功制备了高活性、高稳定性的钨掺杂磷化镍纳米片双功能催化剂,并将其应用于两电极电解体系中,实现了阴、阳极高附加值产物(苯甲腈和氢气)的同时生成.本研究为电化学合成高价值腈化合物和制氢先进催化剂的设计、制备提供了一定的参考和借鉴. 展开更多
关键词 双功能电催化剂 选择性氧化 苯甲腈电合成 脱氢作用 析氢反应
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ZnS-embedded porous carbon for peroxydisulfate activation:Enhanced electron transfer for bisphenol A degradation
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作者 Ying Liu Ningjie Du +4 位作者 Xinru Liu Ducheng Yao deli wu Zhuo Li Shun Mao 《Environmental Science and Ecotechnology》 SCIE 2024年第3期161-169,共9页
Transition metal sulfides have garnered increasing attention for their role in persulfate activation,a crucial process in environmental remediation.However,the function of metal sulfides without reversible valence cha... Transition metal sulfides have garnered increasing attention for their role in persulfate activation,a crucial process in environmental remediation.However,the function of metal sulfides without reversible valence changes,such as ZnS,remains largely unexplored in this context.Here we report ZnS-embedded porous carbon(ZnS-C),synthesized through the pyrolysis of Zn-MOF-74 and dibenzyl disulfide.ZnS-C demonstrates remarkable activity in activating peroxydisulfate(PDS)across a wide pH range,enabling the efficient mineralization removal of bisphenol A(BPA).Through electrochemical investigation and theoretical simulations of charge density distributions,we unveil that the electron transfer from BPA to PDS mediated by the ZnS-C catalyst governs the reaction.This study,both in theory and experiment,demonstrates metal sulfide as electron pump that enhances electron transfer efficiency in PDS activation.These findings redefine the role of metal sulfide catalysts,shedding new light on their potential for regulating reaction pathways in PDS activation processes. 展开更多
关键词 Peroxydisulfate activation Reaction pathway regulation Electron transfer ZNS Bisphenol A
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