过电位
电化学
无机化学
法拉第效率
电解
硝酸盐
化学
可逆氢电极
化学工程
电催化剂
电解质
催化作用
氨生产
材料科学
电极
工作电极
物理化学
工程类
有机化学
生物化学
作者
Yuecheng Xiong,Yunhao Wang,Chi Ching Tsang,Jingwen Zhou,Fengkun Hao,Fu Liu,Juan Wang,Shibo Xi,Jiong Zhao,Zhanxi Fan
标识
DOI:10.1021/acs.est.4c04014
摘要
Electrochemical nitrate reduction (NO3RR) provides a new option to abate nitrate contamination with a low carbon footprint. Restricted by competitive hydrogen evolution, achieving satisfied nitrate reduction performance in neutral media is still a challenge, especially for the regulation of this multielectron multiproton reaction. Herein, facile element doping is adopted to tune the catalytic behavior of IrNi alloy nanobranches with an unconventional hexagonal close-packed (hcp) phase toward NO3RR. In particular, the obtained hcp IrNiCu nanobranches favor the ammonia production and suppress byproduct formation in a neutral electrolyte indicated by in situ differential electrochemical mass spectrometry, with a high Faradaic efficiency (FE) of 85.6% and a large yield rate of 1253 μg cm–2 h–1 at −0.4 and −0.6 V (vs reversible hydrogen electrode (RHE)), respectively. In contrast, the resultant hcp IrNiCo nanobranches promote the formation of nitrite, with a peak FE of 33.1% at −0.1 V (vs RHE). Furthermore, a hybrid electrolysis cell consisting of NO3RR and formaldehyde oxidation is constructed, which are both catalyzed by hcp IrNiCu nanobranches. This electrolyzer exhibits lower overpotential and holds the potential to treat polluted air and wastewater simultaneously, shedding light on green chemical production based on contaminate degradation.
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