材料科学
催化作用
纳米纤维
吸附
化学工程
氧化物
铜
无机化学
碳纳米纤维
单层
氧化还原
硝酸盐
电化学
氢
电催化剂
选择性
析氧
产量(工程)
氧化铜
镓
氧气
作者
Bingbing Liu,Hualei Liu,Siyu Qiang,Jin Dai,Jianhua Yan,Jianyong Yu,Yi‐Tao Liu,Bin Ding
标识
DOI:10.1002/adfm.202529295
摘要
ABSTRACT Suppressing the competing hydrogen evolution reaction (HER) and inefficient mass transport remains a major obstacle for electrocatalytic nitrate reduction reactions (NO 3 RR), particularly in the low nitrate concentration industrial wastewater. Nevertheless, previous studies primarily focus on optimizing catalyst intrinsic activity, yet achieving high selectivity and activity simultaneously remains challenging. Herein, we report a dual coordination strategy to modulate the surface electronic structure and interfacial microenvironment of nanofiber catalysts, thereby enabling simultaneous HER suppression and enhancing electrocatalytic activation of nitrate (). Specifically, the reduced copper species‐modified gallium oxide (r‐Cu/Ga 2 O 3 ) nanofiber catalyst with abundant Cu species and oxygen vacancies is obtained by thermal reduction of the oxide precursor via in situ exsolution method, which enhances the nitrate adsorption and activation. Moreover, a low‐surface‐energy monolayer interface is assembled on nanofiber surface to modulate the reaction microenvironment, restricting proton transfer to active sites and kinetically inhibiting HER. Therefore, the prepared r‐Cu/Ga 2 O 3 ‐SAM nanofiber catalyst achieves NH 3 yield of 22.36 mg h −1 mg −1 at −1.15 V and a FE of 95.48% at −1.05 V versus RHE in 20 mM solution. We expect that these findings can provide novel insights and guidance for designing effective electrocatalytic NO 3 RR catalysts under low NO 3 − concentration.
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