催化作用
离解(化学)
化学
硝酸盐
法拉第效率
无机化学
动力学
产量(工程)
原位
多相催化
废水
化学工程
环境修复
电化学
电催化剂
氧化还原
反应速率
反应机理
反应中间体
化学动力学
质子
作者
Song Chen,Yunyang Qian,Ziyong Cheng,Lai‐Hon Chung,Weihui Ou,Jieying Hu,Quanxi Mo,S. W. Chen,Jun He,Hai‐Long Jiang
摘要
ABSTRACT The electrocatalytic nitrate reduction reaction (eNO 3 RR) offers a sustainable strategy for both NO 3 − wastewater remediation and value‐added NH 3 production. However, its application is hindered by sluggish reaction kinetics in neutral media due to the limited availability of protons. Herein, an anionic metal–organic framework (MOF), SU‐102, is functionalized with atomically dispersed Fe sites to yield SU‐102‐Fe. This catalyst achieves a Faradaic efficiency (FE) of 96.9% and NH 3 production rate of 1.72 mg h −1 mg cat −1 at −0.7 V versus RHE, far surpassing the commercial Fe 2 O 3 and pristine SU‐102. In situ characterizations reveal that the negatively charged Zr─O units in SU‐102 create an anionic microenvironment around the Fe sites, which enriches K + •H 2 O species derived from the interfacial hydrogen‐bonding network. The facile dissociation of K + •H 2 O improves local proton supply, facilitating NO 3 − ‐to‐NH 3 conversion and accounting for the superior eNO 3 RR performance of SU‐102‐Fe.
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