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5篇 您的检索式:作者名="Di IP"
    题名 作者 年代 出处 被引量
1Ovarian steroid and cytokine modulation of human endometrial angiogenesis显示文摘Lebovic DI Shifren JL Ryan IP 2000Hum Reprod2000,153,:1
2Guanosine protects against reperfusion injury in rat brains after ischemie stroke显示文摘Connell B J Di IP Sayeed I 2013J Neuros- ci Res2013,91,2:1
3Oestrogen receptor ER - αand ER - βisoforms in normal endometrial and endometriosis - derived stromal cells 显示文摘Brandenberger AW Lebovic DI Tee MK Ryan IP Tseng JF Jaffe RB and Taylor RN 1999Mol Hum Reprod1999,5,:1
4Remarkable synergistic effect in cobalt-iron nitride/alloy nanosheets for robust electrochemical water splitting显示文摘Design and synthesis of noble-metal-free bifunctional catalysts for efficient and robust electrochemical water splitting are of significant importance in developing clean and renewable energy sources for sustainable energy consumption.Herein,a simple three-step strategy is reported to construct cobalt-iron nitride/alloy nanosheets on nickel foam(CoFe-NA/NF)as a bifunctional catalyst for both hydrogen evolution reaction(HER)and oxygen evolution reaction(OER).The electrocatalyst with optimized composition(CoFe-NA2/NF)can achieve ultralow overpotentials of 73 mV and 250 mV for HER and OER,respectively,at a current density of 10 mA cm^(-2) in 1 M KOH.Notably,the electrolyzer based on this electrocatalyst is able to boost the overall water splitting with a cell voltage of 1.564 V to deliver 10 mA cm^(-2) for at least 50 h without obvious performance decay.Furthermore,our experiment and theoretical calculation demonstrate that the combination of cobalt-iron nitride and alloy can have low hydrogen adsorption energy and facilitate water dissociation during HER.In addition,the surface reconstruction introduces metal oxyhydroxides to optimize the OER process.Our work may pave a new pathway to design bifunctional catalysts for overall water splitting.Mingpeng Chen Di Liu Baoye Zi Yuyun Chen Dong Liu Xinyu Du Feifei Li Pengfei Zhou Ye Ke Jielei Li Kin Ho Lo Chi Tat Kwok Weng Fai Ip Shi Chen Shuangpeng Wang Qingju Liu Hui Pan 2022Journal of Energy Chemistry2022,31,2:0
5How water molecules occupying the active site of a single-atom catalyst affect the electrochemical reduction of carbon dioxide显示文摘In single-atom catalysts(SACs),the single atoms are often exposed as protrusions above the substrate.The solvent molecules in the electrocatalytic environment can interact or even bind to these coordination-unsaturated single atoms and thus influence the reaction process,but this has not been studied in depth.In this work,we systematically investigate the thermodynamics of CO_(2)reduction reaction(CO_(2)RR)to CO over MoS_(2)-supported single metal atom catalysts(TM@MoS_(2),TM=transition metal)under vacuum and explicit solvent environments using density functional theory.In addition,the ab initio molecular dynamics results show that explicit H_(2)O molecules can coordinate to the TM site and undergo competitive adsorption with the CO_(2)RR intermediates,which significantly affects the energy and conformation of the CO_(2)RR pathway.Electronic structure analysis reveals that the occupying H_(2)O molecules change the electronic state of single atom and further influence the adsorption strength of different CO_(2)RR intermediates.Our work shows that water molecules can not only act as ligands to influence the electronic state of TM,but also affect the energy and conformation of CO_(2)RR intermediates,which highlights the important role of occupying H_(2)O molecules at the single-atom sites in CO_(2)RR and provides useful insights for the design of SACs for efficient CO_(2)RR.Jia Zhao Di Liu Fenfei Wei Weng Fai Ip Hui Pan Sen Lin 2023Nano Research2023,16,7:0
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