催化作用
离解(化学)
化学
吸附
亚硝酸盐
氨
Boosting(机器学习)
选择性
无机化学
法拉第效率
分子
选择性催化还原
氨生产
电化学
动力学
化学工程
沸石
电催化剂
水溶液
组合化学
多相催化
反应中间体
还原(数学)
作者
Yangyang Zhang,Zhengkun Xie,Shengxian Ge,Peiyang Li,Xiaotian Wang,Zaiwang Zhao,Zhongyi Liu,Bin Liu,Jun Li
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2025-10-20
卷期号:19 (2): 94908176-94908176
标识
DOI:10.26599/nr.2025.94908176
摘要
Electrocatalytic nitrite reduction reaction (NO2−RR) to synthesize ammonia (NH3) has been constrained by sluggish kinetics of water dissociation and the weak adsorption of nitrite. In this work, we develop an in-situ reconstruction strategy that transforms Ni-doped BiO2-x (NiBiO2-x) to Bi/NiBiO2-x, which exhibits excellent activity and selectivity for NO2−RR to synthesize NH3. Diverse ex-situ and in-situ characterizations reveal potential-driven structural transformation from NiBiO2-x to Bi/NiBiO2-x, which features dual Ni2+-Bi0 active sites. The Ni2+ site is able to reduce the water dissociation barrier from 0.79 to 0.41 eV, while concurrently the Bi0 site can strengthen NO2− adsorption to promote *NO2H intermediate formation. Consequently, the in-situ constructed Bi/NiBiO2-x catalyst with Ni2+-Bi0 catalytic pairs enable an excellent NO2−RR performance, achieving a NH3 Faradaic efficiency (FENH3) of 94.5% at −0.6 V vs. RHE. The present study opens the new direction to in-situ construct high-performance electroreduction catalysts for small molecule synthesis.
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