钴
甲醇
无机化学
铜
氧化钴
化学
电催化剂
电极
硝酸盐
氧化还原
电化学
有机化学
物理化学
作者
Xiuge Wang,Junhao Ren,Zhiyong Gao
标识
DOI:10.1016/j.jcis.2025.137575
摘要
Self-supported Cu-CoO/NF was fabricated by electrodeposition , the synergy of Cu and CoO components led to high NO 3 RR efficiency, the Cu-CoO/NF also demonstrated considerable MOR property. The bifunctional catalytic features enabled pairwise production of NH 3 and formate chemicals by electrolysis. • ·Sel-supported Cu-CoO/NF was designed for NO 3 RR and MOR bifunctional catalysis. • ·The relay effects of Cu and CoO components enabled high NO 3 RR performance. • ·NH 3 and formate were coproduced at high FEs, yields and low energy consumption. Electrochemical nitrate reduction reaction (NO 3 RR) to ammonia (NH 3 ) is a sustainable approach to upcycle nitrate (NO 3 − ) pollutant, the further pairing of cathodic NO 3 RR with anodic methanol oxidation reaction (MOR) enables coproduction of NH 3 and formate chemicals by electrolysis at enhanced energy efficiency. Bifunctional catalytic electrode for both reactions is crucial for achieving such a target. In view of the strong NO 3 − adsorption ability of copper (Cu) and the high active hydrogen adsorption ability of cobalt (Co) based compound, the catalyst composed of Cu and Co elements facilitates the deoxidation and complete hydrogenation of NO 3 − into NH 3 . In addition, the Cu- and Co-containing material is also possible catalyst or precatalyst for MOR. Herein, a self-supported Cu-cobalt oxide (CoO) hybrid onto nickel foam substrate, denoted as Cu-CoO/NF electrode, was fabricated by electrodeposition at negative potential. Due to the relaying effect of Cu and CoO components during NO 3 RR, the Cu-CoO/NF achieved a decent faradaic efficiency (FE) of 84 ± 4 % and an NH 3 yield of 0.40 ± 0.02 mmol h −1 cm −2 at a high operation potential of −0.1 V. Moreover, the Cu-CoO/NF demonstrated high MOR property for formate production at significantly reduced potential (over 0.2 V) compared to the oxygen evolution reaction. The NO 3 RR-MOR coelectrolyser enabled coproduction of NH 3 and formate at reduced energy consumption. This work provides a promising paradigm for pairwise production of valuable chemicals via rational design of catalytic electrode and construction of coelectrolysis system.
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