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用于增强电催化硝酸盐制氨选择性的铜上硫增强活性氢

Sulphur-Boosted Active Hydrogen on Copper for Enhanced Electrocatalytic Nitrate-to-Ammonia Selectivity.

作者信息

Xu Yue, Cheng Chuanqi, Zhu Jiewei, Zhang Bin, Wang Yuting, Yu Yifu

机构信息

School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300350, China.

Department of Chemistry, Institute of Molecular Plus, School of Science, Tianjin University, Tianjin, 300350, China.

出版信息

Angew Chem Int Ed Engl. 2024 Apr 15;63(16):e202400289. doi: 10.1002/anie.202400289. Epub 2024 Mar 7.

Abstract

Electrocatalytic nitrate reduction to ammonia is a promising approach in term of pollutant appreciation. Cu-based catalysts performs a leading-edge advantage for nitrate reduction due to its favorable adsorption with *NO. However, the formation of active hydrogen (*H) on Cu surface is difficult and insufficient, leading to the significant generation of by-product NO . Herein, sulphur doped Cu (Cu-S) is prepared via an electrochemical conversion strategy and used for nitrate electroreduction. The high Faradaic efficiency (FE) of ammonia (98.3 %) and an extremely low FE of nitrite (1.4 %) are achieved on Cu-S, obviously superior to its counterpart of Cu (FE: 70.4 %, FE : 18.8 %). Electrochemical in situ characterizations and theoretical calculations indicate that a small amount of S doping on Cu surface can promote the kinetics of HO dissociation to active hydrogen. The optimized hydrogen affinity validly decreases the hydrogenation kinetic energy barrier of *NO, leading to an enhanced NH selectivity.

摘要

从污染物增值的角度来看,电催化硝酸盐还原制氨是一种很有前景的方法。铜基催化剂因其对*NO的良好吸附而在硝酸盐还原方面具有前沿优势。然而,在铜表面形成活性氢(H)困难且不足,导致大量副产物NO生成。在此,通过电化学转化策略制备了硫掺杂铜(Cu-S)并用于硝酸盐电还原。在Cu-S上实现了较高的氨法拉第效率(FE)(约98.3%)和极低的亚硝酸盐FE(约1.4%),明显优于其对应的铜(FE:70.4%,FE:18.8%)。电化学原位表征和理论计算表明,在铜表面少量掺杂硫可以促进HO解离为活性氢的动力学。优化后的氢亲和力有效降低了NO的加氢动能垒,从而提高了NH的选择性。

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