乙二醇
材料科学
法拉第效率
钴
铜
可逆氢电极
无机化学
催化作用
电催化剂
电解
阳极
亚硝酸盐
氧化钴
氨
氧化物
化学工程
电化学
工作电极
有机化学
电极
冶金
化学
电解质
硝酸盐
物理化学
工程类
作者
Zhaodong Niu,Shiying Fan,Xinyong Li,Guohua Chen
标识
DOI:10.1002/aenm.202303515
摘要
Abstract Electrocatalytic nitrite (NO 2 − ) reduction reaction (NO 2 − RR) for ammonia (NH 3 ) synthesis is a promising alternative for NO 2 − resource utilization. Herein, a dual‐site copper‐cobalt oxide catalyst is reported for the efficient electrocatalytic reduction of NO 2 − to NH 3 , exhibiting NH 3 Faradaic efficiency that remained above 95% (0.1 m NaNO 2 ) over a wide potential window (−0.1 to −0.6 V vs reversible hydrogen electrode, vs RHE). More importantly, the high NH 3 Faradaic efficiency maintains an over 85% (−0.1 to −0.3 V vs RHE) at a low concentration of NaNO 2 (0.01 m ). Theoretical calculations demonstrate that CuO serves the * NO 2 to * NO and is subsequently converted to NH 3 on Co 3 O 4 . Coupled anodic ethylene glycol (EG) oxidation reaction endows low cell voltage (ΔU = 480 mV, 10 mA cm −2 ) and energy consumption saving (>23%) in a two‐electrode system. This work provides a reference for a co‐upcycling electrolyzer for NO 2 − and EG.
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