锑
催化作用
电合成
法拉第效率
产量(工程)
化学
无机化学
电催化剂
氧化物
Atom(片上系统)
无定形固体
金属
材料科学
电化学
组合化学
电极
物理化学
有机化学
冶金
嵌入式系统
计算机科学
作者
Kai Chen,Ying Zhang,Jiaqi Xiang,Xiaolin Zhao,Xingang Li,Ke Chu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-02-03
卷期号:8 (3): 1281-1288
被引量:141
标识
DOI:10.1021/acsenergylett.2c02882
摘要
Electrocatalytic NO reduction to NH3 (NORR) offers a prospective approach to attain both harmful NO removal and efficient NH3 electrosynthesis. Main-group p-block metals are promising NORR candidates but still lack adequate exploration. Herein, p-block Sb single atoms confined in amorphous MoO3 (Sb1/a-MoO3) are designed as an efficient NORR catalyst, exhibiting the highest NH3 yield rate of 273.5 μmol h–1 cm–2 and a NO-to-NH3 Faradaic efficiency of 91.7% at −0.6 V vs RHE. In situ spectroscopic characterizations and theoretical computations reason that the outstanding NORR performance of Sb1/a-MoO3 arises from the isolated Sb1 sites, which can optimize the adsorption of *NO/*NHO to lower the reaction energy barriers and simultaneously exhibit a higher affinity to NO than to H2O/H species. Moreover, our strategy can be extended to prepare Bi1/a-MoO3, showing a high NORR property, demonstrating the immense potential of p-block metal single-atom catalysts toward the high-performing NORR electrocatalysis.
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