亚硝酸盐
催化作用
化学
氨
无机化学
产量(工程)
质子化
选择性
电子转移
电合成
氨生产
基质(水族馆)
氢
光化学
电化学
有机化学
物理化学
材料科学
硝酸盐
离子
地质学
冶金
海洋学
电极
作者
Wenyu Du,Ying Zhang,Kai Chen,Guike Zhang,Ke Chu
标识
DOI:10.1016/j.jclepro.2023.138875
摘要
Electrocatalytic nitrite reduction to ammonia (NO2RR) presents an efficient approach for both wastewater treatment and powerful ammonia electrosynthesis. However, the activity and selectivity of NO2RR are limited by its complex six−electron transfer process and competitive hydrogen evolution. Herein, Mo single atoms anchored on a zirconium dioxide substrate (Mo1–ZrO2) are first explored as a highly selective and active catalyst for the NO2RR, exhibiting a maximum NH3−Faraday efficiency of 94.83% with a corresponding ammonia yield rate of 346.92 μmol h−1 cm−2 at −0.7 V vs. RHE. Theoretical calculations reveal that the isolated Mo sites can effectively activate nitrite, enhance nitrite−to−ammonia protonation energetics and prohibit competitive hydrogen evolution, thus leading to the remarkably enhanced selectivity and activity of Mo1–ZrO2 for the NO2RR.
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