密度泛函理论
合理设计
催化作用
氢
Atom(片上系统)
氧原子
材料科学
氢原子
金属
过渡金属
化学物理
氧气
化学
计算化学
纳米技术
分子
群(周期表)
计算机科学
有机化学
冶金
嵌入式系统
生物化学
作者
Suman Kalyan Sahoo,Youngjin Ye,Seonggyu Lee,Jinkyu Park,Hyunjoo Lee,Jinwoo Lee,Jeong Woo Han
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-11-19
卷期号:4 (1): 126-132
被引量:124
标识
DOI:10.1021/acsenergylett.8b01942
摘要
We use a combination of density functional theory (DFT) calculations and experimental approaches to explore the stability and electrocatalytic activity of a wide range of transition-metal single atoms on a TiC support. Our theoretical prediction that single atoms can be stabilized on the modified TiC surface is confirmed by experimental findings using them on a TiC support. The predicted activities where Pt and Au single atoms would be the best for hydrogen evolution and selective oxygen reduction reactions, respectively, agree well with experimental results. This rational strategy using computational modeling of materials enables effective design of highly active and stable single-atom catalysts.
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