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Achieving asymmetric redox chemistry for oxygen evolution reaction through strong metal-support interactions
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作者 Shihao Wang meiling fan +4 位作者 Hongfei Pan Jiahui Lyu Jinsong Wu Haolin Tang Haining Zhang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第9期526-535,共10页
Water electrolysis poses a significant challenge for balancing catalytic activity and stability of oxygen evolution reaction(OER)electrocatalysts.In this study,we address this challenge by constructing asymmetric redo... Water electrolysis poses a significant challenge for balancing catalytic activity and stability of oxygen evolution reaction(OER)electrocatalysts.In this study,we address this challenge by constructing asymmetric redox chemistry through elaborate surface OO–Ru–OH and bulk Ru–O–Ni/Fe coordination moieties within single-atom Ru-decorated defective NiFe LDH nanosheets(Ru@d-NiFe LDH)in conjunction with strong metal-support interactions(SMSI).Rigorous spectroscopic characterization and theoretical calculations indicate that single-atom Ru can delocalize the O 2p electrons on the surface and optimize d-electron configurations of metal atoms in bulk through SMSI.The^(18)O isotope labeling experiment based on operando differential electrochemical mass spectrometry(DEMS),chemical probe experiments,and theoretical calculations confirm the encouraged surface lattice oxygen,stabilized bulk lattice oxygen,and enhanced adsorption of oxygen-containing intermediates for bulk metals in Ru@d-NiFe LDH,leading to asymmetric redox chemistry for OER.The Ru@d-NiFe LDH electrocatalyst exhibits exceptional performance with an overpotential of 230 mV to achieve 10 mA cm^(−2)and maintains high robustness under industrial current density.This approach for achieving asymmetric redox chemistry through SMSI presents a new avenue for developing high-performance electrocatalysts and instills confidence in its industrial applicability. 展开更多
关键词 Reaction redox chemistry Strong metal-support interactions Layered double hydroxides ELECTROCATALYSTS Water electrolysis
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A mini-review on pharmacological effects of ginsenoside Rb3,a marked saponin from Panax genus 被引量:1
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作者 WEI LI YUEYANG DUAN +3 位作者 XIAOTONG YAN XIANGXIANG LIU meiling fan ZI WANG 《BIOCELL》 SCIE 2022年第6期1417-1423,共7页
Ginsenoside Rb3(G-Rb3)is one of the primary active compounds isolated from Panax ginseng Meyer,which belongs to protopanaxadiol ginsenosides(PPD).Based on the structure-activity relationship(SAR)of ginsenosides,the pe... Ginsenoside Rb3(G-Rb3)is one of the primary active compounds isolated from Panax ginseng Meyer,which belongs to protopanaxadiol ginsenosides(PPD).Based on the structure-activity relationship(SAR)of ginsenosides,the pentose structure of G-Rb3 limited itself to possess more pharmacological activity to a certain extent.However,pharmacokinetics show that G-Rb3 is processed through deglycosylation in the intestinal tract and converted into more active rare saponins,such as Compound K,F2,etc.A series of studies focused on neuroprotection and the cardiovascular system demonstrating its therapeutic potentials,which was achieved by diminishing oxidative stress and apoptosis.Therefore,more systematic and in-depth studies are needed to complete the pharmaceutical value and to promote its clinical applications.This article highlights the multiple pharmacological effects and mechanisms of G-Rb3 and prospects for its development. 展开更多
关键词 Ginsenoside Rb3 Pharmacological effects Review Signaling pathway
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纳米零价铁对水溶液中钒离子的吸附性能
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作者 赵长多 杨晓博 +2 位作者 范美玲 胡文斌 夏启斌 《过程工程学报》 CAS CSCD 北大核心 2018年第6期1253-1260,共8页
采用液相还原法制备纳米零价铁(nZVI),采用PXRD,SEM,TEM,BET(N2吸脱附)和XPS等表征材料性能,考察了纳米零价铁用量、初始钒(V)浓度和初始pH对纳米零价铁吸附钒(V)性能的影响,测定了纳米零价铁对钒(V)的吸附等温线和吸附动力学曲线.结果... 采用液相还原法制备纳米零价铁(nZVI),采用PXRD,SEM,TEM,BET(N2吸脱附)和XPS等表征材料性能,考察了纳米零价铁用量、初始钒(V)浓度和初始pH对纳米零价铁吸附钒(V)性能的影响,测定了纳米零价铁对钒(V)的吸附等温线和吸附动力学曲线.结果表明,制备的纳米零价铁具有典型的核-壳结构,粒径为10~30nm,BET比表面积为53m^2/g.纳米零价铁对钒(V)的吸附容量随纳米零价铁用量和初始pH增大而减小.25℃时的平衡吸附容量为227.8mg/g.Langmuir等温线方程可很好拟合纳米零价铁对钒(V)的吸附,纳米零价铁对钒(V)的吸附动力学曲线符合准二级动力学模型. 展开更多
关键词 选择性催化还原催化剂 纳米零价铁 吸附 动力学
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