FCF-LDH/BiVO4 with synergistic effect of physical enrichment and chemical adsorption for efficient reduction of nitrate

吸附 化学 催化作用 选择性 电解质 无机化学 路易斯酸 核化学 电极 有机化学 物理化学
作者
Yajie Bai,Zhenyuan Fang,Yong Lei,Lijing Liu,Huaiquan Zhao,Hongye Bai,Weiqiang Fan,Weidong Shi
出处
期刊:Green Energy & Environment [KeAi]
被引量:2
标识
DOI:10.1016/j.gee.2023.05.011
摘要

Photoelectrochemical NO3− reduction (PEC NITRR) not only provides a promising solution for promoting the global nitrogen cycle, but also converts NO3− to the important chemicals (NH3). However, it is still a great challenge to prepare catalysts with excellent NO3− adsorption/activation capacity to achieve high NITRR. Herein, we designed a novel Fe2+Cu2+Fe3+LDH/BiVO4 (FCF-LDH/BVO) catalyst with synergistic effect of chemical adsorption and physical enrichment. Fe2+ in FCF-LDH/BVO provides the rich Lewis acid sites for the adsorption of NO3−, and the appropriate layer spacing of FCF-LDH further promotes the physical enrichment of NO3− in its interior, thus realizing the effective contact between NO3− and active sites (Fe2+). FCF-LDH/BVO showed excellent NH3 production performance (FENH3 = 66.1%, rNH3 = 13.8 μg h−1 cm−2) and selectivity (FENO2- = 2.5%, rNO2- = 4.9 μg h−1 cm−2) in 0.5M Na2SO4 electrolyte. In addition, FCF-LDH/BVO maintains the desirable PEC stability for six cycle experiments, showing great potential for practical application. The 14NO3− and 15NO3− isotope test provides strong evidence for further verification of the origin of N in the generated NH3. This LDH catalyst has a great potential in PEC removal of NO3− from groundwater.

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