催化作用
X射线吸收光谱法
材料科学
结晶学
吸收光谱法
原子轨道
Atom(片上系统)
化学
纳米技术
电子
有机化学
计算机科学
物理
量子力学
嵌入式系统
作者
Lei Zhang,Qi Wang,Rutong Si,Zhongxin Song,Xiaoting Lin,Mohammad Norouzi Banis,Keegan R. Adair,Junjie Li,Kieran Doyle‐Davis,Ruying Li,Limin Liu,Meng Gu,Xueliang Sun
出处
期刊:Small
[Wiley]
日期:2021-02-03
卷期号:17 (16)
被引量:61
标识
DOI:10.1002/smll.202004453
摘要
Abstract Single atomic Pt catalysts exhibit particularly high hydrogen evolution reaction (HER) activity compared to conventional nanomaterial‐based catalysts. However, the enhanced mechanisms between Pt and their coordination environment are not understood in detail. Hence, a systematic study examining the different types of N in the support is essential to clearly demonstrate the relationship between Pt single atoms and N‐doped support. Herein, three types of carbon nanotubes with varying types of N (pyridine‐like N, pyrrole‐like N, and quaternary N) are used as carbon support for Pt single atom atomic layer deposition. The detailed coordination environment of the Pt single atom catalyst is carefully studied by electron microscope and X‐ray absorption spectra (XAS). Interestingly, with the increase of pyrrole‐like N in the CNT support, the HER activity of the Pt catalyst also improves. First principle calculations results indicate that the interaction between the dyz and s orbitals of H and sp 3 hybrid orbital of N should be the origin of the superior HER performance of these Pt single atom catalysts (SACs).
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