DOI码：10.1039/D3TA04385A
发表刊物：Journal of Materials Chemistry A
摘要：The process of electrocatalytic nitrate reduction reaction (NIRR) to produce ammonia (NH 3) presents a promising solution to the challenges of nitrate contamination and high value ammonia synthesis. However, owing to the eight-electron reaction of NIRR, the cathode catalyst type plays a crucial role in governing the NIRR. Herein, Cu 1 Co 1-BCN was prepared as an electrochemical cathode catalyst for the conversion of NO 3 − to NH 3 using a dodecahydro-closo-dodecaborate hybrid (closo-[B 12 H 12 ] 2−). The catalyst exhibited an excellent ammonia yield (6412.06 mg h −1 mg cat −1) at −0.5 V versus the reversible hydrogen electrode and a Faraday efficiency (FE) of 92.44%. Additionally, Cu 1 Co 1-BCN exhibited remarkable resistance to interference in 10 mM interfering ion solutions and excellent resistance to acids and bases even at extreme pH levels. It also showed almost no variation in the ammonia yield and FE over ten experimental cycles, thereby indicating its remarkable stability. Furthermore, density functional theory (DFT) calculations confirmed the likelihood of the occurrence of the intermediate step (*N / *NH), adsorption of NO 3 − , and desorption of NH 3 by Cu 1 Co 1-BCN, thereby facilitating the conversion of NO 3 − to NH 3. These findings offer new insights with regard to designing catalysts for green electrocatalytic ammonia synthesis.
论文类型：期刊论文
论文编号：10.1039/D3TA04385A
学科门类：理学
文献类型：J
期号：11
页面范围：20234-20241
是否译文：否
发表时间：2023-09-11
收录刊物：SCI、EI
发布期刊链接：https://doi.org/10.1039/D3TA04385A
发表时间：2023-09-11