过电位
析氧
制氢
电合成
分解水
电化学
氢
钌
密度泛函理论
化学
二硫化钼
计算化学
化学工程
催化作用
有机化学
物理化学
电极
光催化
工程类
作者
Cong Zhang,Chi Zhang,Jiachen Li,Yuqiang Ma,Wujing Jin,Zhaoqi Guo,Xingqiang Lü,Hua Ma
标识
DOI:10.1016/j.apsusc.2022.155659
摘要
The electrochemical water splitting process is comprised of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), where the OER is usually the bottleneck of the whole reaction, causing the high overpotential, while the oxidation product (O2) is of less economic value. In this article, we report a new coupling system based on the green electro-oxidation synthesis of energetic compounds and simultaneous H2 production on the molybdenum disulfide/ruthenium-based single-atom catalyst (Ru SAs MoS2/CC). The charge redistribution and synergistic interaction between MoS2 and Ru SAs for alkaline HER were systemically investigated by experimental and density functional theory (DFT) calculation. More importantly, the integration of overall water splitting (OWS) and anodic N-N oxidative coupling of 5-amino-1H-tetrazole (5-AT) shows an ultralow cell voltage of 1.36 V at 10 mA cm−2 for the H2 production and simultaneously realize green-synthesis of dipotassium 5,5′-azotetrazole (K2AZT), which is traditionally synthesized under harsh condition requiring high temperature and excessive oxidant. This work highlights a unique strategy for energy-saving H2 production and eco-friendly electrosynthesis of energetic compounds.
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