Efficient Co and GO co-doped TiO2 catalysts for the electrochemical reduction of nitrate to ammonia

被引:0
|
作者
Lin, Peiyan [1 ,2 ]
Chen, Renhong [1 ]
Xu, Sheng [1 ]
Xia, Xia [1 ]
Zhao, Fang [1 ]
Ren, Xuefeng [1 ]
Lu, Yumeng [1 ]
Gao, Liguo [1 ]
Bao, Junjiang [1 ]
Liu, Anmin [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn Ocean & Life Sci, Panjin 124221, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing, Peoples R China
关键词
NITROGEN;
D O I
10.1039/d4cy01228c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrocatalytic nitrate (NO3-) reduction to ammonia (NH3) has emerged as an environmentally friendly method for ammonia production due to its clean, efficient, and sustainable attributes. In this study, we prepared Co-doped TiO2 materials with graphene oxide (GO), Co-TiO2/GO, as potential NO3-RR electrocatalysts. Scanning electron microscopy (SEM) images revealed a spherical structure for the catalysts. Following a series of electrochemical tests, our findings indicated that Co-doping significantly enhances the NO3-RR activity of TiO2. Furthermore, incorporating GO notably diminishes the initial potential of titania-based catalysts, thereby strengthening the NO3-RR performance of TiO2. The engineered Co-TiO2/GO exhibits superior NO3-RR electrochemical properties, achieving an NH3 yield of up to 7.424 mg h-1 cm-2 and a Faraday efficiency of up to 56.5% at -1.1 V vs. RHE potential. This performance surpasses that of Co-TiO2, with minimal by-product NO2- generation. We also conducted tests without the catalyst and in the absence of NO3- in the electrolyte, confirming that the nitrogen in the synthesized ammonia was not derived from impurities in the catalyst or the electrolyte. Furthermore, Co-TiO2/GO demonstrated robust stability during eight cycles and 24 hours of continuous testing for the NO3-RR performance. Theoretical calculations suggest that doping TiO2 with Co and GO can enhance its electronic structure and conductivity, thereby facilitating the electrochemical synthesis of ammonia.
引用
收藏
页码:1445 / 1455
页数:11
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