催化作用
电化学
色散(光学)
氮原子
金属
氮气
还原(数学)
Atom(片上系统)
材料科学
无机化学
化学
光化学
物理化学
电极
有机化学
冶金
光学
物理
几何学
数学
计算机科学
群(周期表)
嵌入式系统
作者
Yibing Sun,Jing‐Shuang Dang,Xiang Zhao
标识
DOI:10.1002/cctc.202401262
摘要
The present study delves into electrochemical nitrogen reduction reaction (NRR) for ammonia synthesis using borophane‐supported single‐atom catalysts (SACs) through density functional theory (DFT) calculations. In comparison to previously reported borophene, which serves as a potential substrate for SACs in NRR, hydrogenated borophane, especially borophane‐2H, not only prevents metal aggregation, resulting in stable atomically dispersed metal centers, but also enhances catalytic activity by modulating the metal's charge state. Among all candidates, atomic tungsten anchored W/borophane‐2H displays the most favorable NRR activity and product selectivity.
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