Promoting active hydrogen supply for kinetically matched tandem electrocatalytic nitrate reduction to ammonia

Biyu Kang, Bincheng Xu, Zhixuan Chen, Fengting Li, Ying Wang
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Abstract

Electrocatalytic nitrate reduction (NORR) shows admirable potential for environmental remediation and producing valuable NH. However, the catalyst is restricted by the kinetic mismatch between NO-to-NO and NO-to-NH, which results in excess NO and poor NH selectivity. Herein, a kinetically matched tandem electrocatalytic strategy with tunable active hydrogen(*H) supply is designed. The combination of CuO and Co(HPO)(OH) (CoPO) playing key roles in NORR by i) on-demand supply of *H from CoPO; ii) the electronically coupled interface between CuO and CoPO enhance *H transfer kinetics. The CuO-CoPO-2 exhibits high NH yield of 22 mg cm h with Faradaic efficiency of 95 % at −0.37 V vs. RHE. In situ characterizations indicate the dynamic equilibrium between *H production and consumption contributes to high NORR performance. The techno-economic analyses reveal the system is economically viable compared to Haber-Bosch (H-B) process, which benefits from industrial current densities and superior energy efficiency at low potentials.
促进主动供氢,实现与动力学匹配的串联电催化硝酸盐还原成氨
电催化硝酸盐还原(NORR)在环境修复和生产有价值的 NH 方面显示出令人钦佩的潜力。然而,催化剂受到 NO 转化为 NO 和 NO 转化为 NH 之间动力学不匹配的限制,导致 NO 过量和 NH 选择性差。在此,我们设计了一种具有可调活性氢(*H)供应的动力学匹配串联电催化策略。CuO 和 Co(HPO)(OH)(CoPO)的组合在 NORR 中发挥了关键作用:i)CoPO 按需提供*H;ii)CuO 和 CoPO 之间的电子耦合界面提高了*H 转移动力学。CuO-CoPO-2 的 NH 产率高达 22 mg cm h,在 -0.37 V 对 RHE 时的法拉第效率为 95%。原位特性分析表明,*H 生成和消耗之间的动态平衡有助于提高 NORR 性能。技术经济分析表明,与哈伯-博什(H-B)工艺相比,该系统在经济上是可行的,因为哈伯-博什工艺在低电位时具有工业电流密度和卓越的能效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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