催化作用
掺杂剂
等离子体
氢
电子转移
化学
密度泛函理论
Atom(片上系统)
协调数
物理化学
材料科学
兴奋剂
计算化学
离子
有机化学
嵌入式系统
物理
量子力学
光电子学
计算机科学
作者
Jing Li,Yanan Zhou,Weijing Tang,Jian Zheng,Xiaoping Gao,Ning Wang,Xiao Chen,Min Wei,Xin Xiao,Wei Chu
标识
DOI:10.1016/j.apcatb.2020.119861
摘要
Coordination tunability of the single-atom catalysts (SACs) is an essential but challenging issue for the catalyst sifting and structure-activity relationship analysis. Herein, Pt single atoms with tunable coordination are readily achieved via a facile cold-plasma technique by changing the gas type (N2, Ar, or Air) and treatment duration. Combining with density functional theory calculation, the Pt-N coordination concentration is predicted to be highly correlated with adsorption free energy of H* atoms (ΔGH*) for the hydrogen evolution reaction (HER), which is further validated experimentally. Remarkably, the sample with N, O co-dopant introduced by air plasma exhibits a high TOF of ∼13 H2 s−1 at 40 mV, and outstanding mass activity of 7.41 A mg−1Pt for HER, which is 26.5 times of commercial Pt/C catalyst. The enhanced performance might originate from the optimized electronic structure of active carbon site with moderate electron transfer and p-band center, which enables a suitable binding strength with H* and thus a near-zero ΔGH*.
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