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Nano-Polycrystalline Cu Layer Interlaced with Ti3+-Self-Doped TiO2 Nanotube Arrays as an Electrocatalyst for Reduction of Nitrate to Ammonia

The electrochemical nitrate reduction reaction (NO3RR) is considered as a promising strategy to degrade nitrate-containing wastewater and synthesize recyclable ammonia at atmospheric pressure and room temperature. In this work, the copper oxides-derived nano-polycrystalline Cu (NPC Cu) was integrate...

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Published in:ACS applied materials & interfaces 2023-04, Vol.15 (13), p.16680-16691
Main Authors: Chen, Mingfei, Zhuang, Shuxian, Cheng, Jinlu, Miao, Jinyuan, Tai, Xuefeng, Gu, Yinghua, Qin, Zhiwei, Zhang, Jinpeng, Tang, Yang, Sun, Yanzhi, Wan, Pingyu
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Language:English
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Summary:The electrochemical nitrate reduction reaction (NO3RR) is considered as a promising strategy to degrade nitrate-containing wastewater and synthesize recyclable ammonia at atmospheric pressure and room temperature. In this work, the copper oxides-derived nano-polycrystalline Cu (NPC Cu) was integrated with Ti3+-self-doped TiO2 nanotube arrays (NTA) to fabricate the NPC Cu/H–TiO2 NTA. Ti3+-self-doped TiO2 NTAs and the NPC Cu facilitate electron transfer and mass transportation and create abundant active sites. The unique nanostructure in which Cu nano-polycrystals interlace with the TiO2 nanotube accelerates the electron transfer from the substrate to surface NPC Cu. The density functional theory calculations confirm that the built-in electric field between Cu and TiO2 improves the adsorption characteristic of the NPC Cu/H–TiO2 NTA, thereby converting the endothermic NO3 – adsorption step into an exothermic process. Therefore, the high NO3 – conversion of 98.97%, the Faradic efficiency of 95.59%, and the ammonia production yield of 0.81 mg cm–2 h–1 are achieved at −0.45 V vs reversible hydrogen electrode in 10 mM NaNO3 (140 mg L–1)–0.1 M Na2SO4. This well-designed NPC Cu/H–TiO2 NTA as an effective electrocatalyst for the 8e– NO3RR possesses promising potential in the applications of ammonia production.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.2c22399