材料科学
电子转移
电催化剂
催化作用
过渡金属
价电子
价(化学)
电子
化学物理
原子单位
纳米技术
氧化还原
原子物理学
物理化学
电化学
化学
电极
物理
冶金
有机化学
量子力学
生物化学
作者
Mingzi Sun,Tong Wu,Yurui Xue,Alan William Dougherty,Bolong Huang,Yuliang Li,Chengxi Yan
出处
期刊:Nano Energy
[Elsevier]
日期:2019-08-01
卷期号:62: 754-763
被引量:64
标识
DOI:10.1016/j.nanoen.2019.06.008
摘要
Atomic catalysts (AC) as the frontier in atomic catalyst have attracted tremendous attention in recent electrocatalyst research. The performance of ACs strongly depends on the electronic interaction between the atoms and support. To supply a direct strategy for discovering more promising electrocatalysts, we propose a comprehensive mapping study of anchoring transition metals on the graphdiyne (GDY). The electron transfer ability and zero-valence stability are quantified based on the redox process between surface metal and GDY support. The different electron transfer number and directions between the transition metals and GDY are also compared, in which the initial one-electron transfer is the most difficult. Among all the TMs, Co, Pd and Pt have displayed the exceptional stability of zero-valence catalyst based on the evident energy barrier difference between losing electrons and gaining electrons. Experimental results support the remarkable performance of our screened candidates, which have opened a new possibility to achieve novel high-performance zero-valence ACs. Moreover, we outlook the introduction of the deep-learning algorithm in the future advanced mapping strategy for achieving more complicated ACs. This work not only supplies innovative electrocatalyst candidates but also exhibits an innovative approach for studying the electrocatalysts that can further apply to more material systems.
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