Improved NH3-N conversion efficiency to N2 activated by BDD substrate on NiCu electrocatalysis process

电催化剂 催化作用 基质(水族馆) X射线光电子能谱 双金属片 拉曼光谱 亚硫酸盐 可逆氢电极 无机化学 阳极 水溶液 选择性 化学 材料科学 化学工程 光化学 工作电极 电化学 工程类 物理化学 电极 生物化学 地质学 物理 光学 海洋学
作者
Jing-Jin Song,Yinhai Yang,Yingna Jia,Tingting Wang,Jun Wei,Mingming Wang,Shaodong Zhou,Zhongjian Li,Yang Hou,Lecheng Lei,Bin Yang
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:276: 119350-119350 被引量:24
标识
DOI:10.1016/j.seppur.2021.119350
摘要

We developed a novel boron-doped diamond (BDD) electrode by the modification of bimetallic NiCu catalysts via electrochemical co-deposition method for improving the NH3-N conversion efficiency and selectivity to N2 in aqueous solution. It shows that the N2 selectivity of ammonia oxidation reaction (AOR) reached 88.62% with the NH3-N oxidation efficiency of 44.8% in 6 h. The high current efficiency of 84.17% was achieved at 1.2 V (vs Ag/AgCl), and the energy consumption was 8.19 kW·h/(kgN). Furthermore, the reaction mechanism has been investigated by in-situ Raman spectra, X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) during the reaction. It is verified that the BDD substrate plays a crucial role not only in the improvement of electronic transmission rate and but also the generation of abundant hydroxyl radicals (·OH) which provide proper hydrogen acceptors for the N-H bond activation processes. Theoretical calculations further reveal the doping effect of Cu(OH)2 with NiOOH that constructs the Cu/Ni concerted metal-nitrogen interaction, which stabilizes the relative energies of the intermediates thus promoting the reaction. This work sheds new light on the mechanism of selective electrochemical oxidation of NH3-N and develops an innovative technology of catalytic anode design toward wastewater treatment.
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