双功能
脱氢
析氧
化学
水溶液
电解
氧化还原
制氢
阳极
电极
无机化学
分解水
标准氢电极
法拉第效率
氢
纳米片
组合化学
化学工程
电化学
催化作用
有机化学
工作电极
光催化
物理化学
工程类
电解质
作者
Chenqi Huang,Yi Huang,Cuibo Liu,Yifu Yu,Bin Zhang
标识
DOI:10.1002/ange.201903327
摘要
Abstract Exploring an alternative anodic reaction to produce value‐added chemicals with high selectivity, especially integrated with promoted hydrogen generation, is desirable. Herein, a selective semi‐dehydrogenation of tetrahydroisoquinolines (THIQs) is demonstrated to replace the oxygen evolution reaction (OER) for boosting H 2 evolution reaction (HER) in water over a Ni 2 P nanosheet electrode. The value‐added semi‐dehydrogenation products, dihydroisoquinolines (DHIQs), can be selectively obtained with high yields at the anode. The controllable semi‐dehydrogenation is attributed to the in situ formed Ni II /Ni III redox active species. Such a strategy can deliver a variety of DHIQs bearing electron‐withdrawing/donating groups in good yields and excellent selectivities, and can be applied to gram‐scale synthesis. A two‐electrode Ni 2 P bifunctional electrolyzer can produce both H 2 and DHIQs with robust stability and high Faradaic efficiencies at a much lower cell voltage than that of overall water splitting.
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