期刊
ENVIRONMENTAL SCIENCE-NANO
卷 9, 期 8, 页码 2841-2853出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2en00421f
关键词
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资金
- National Natural Science Foundation of China [21876052, U21A2034]
- Guangdong Special Support Plan for Innovation Teams [2019BT02L218]
- Guangdong Special Support Plan for Young Top-notch Talents [2019TQ05L179]
- Science and Technology Planning Project of Guangdong Province, China [2019A050510009]
- Natural Science Foundation of Guangdong Province, China [2021B1515120077]
Metal-encapsulated and nitrogen-doped carbon-based (M@NC) catalysts have shown excellent activity and stability in electrochemical nitrate reduction reaction (ENRR). However, their denitrification performance is unsatisfactory at high current density. In this study, a free-standing M@NCNT array on carbon cloth (CC) was synthesized to address this issue. The unique standing-up structure allows for more active centers and improves the utilization and overall performance. The Co@NCNT/CC cathode exhibited outstanding denitrification activity and stability in ENRR and showed effectiveness in removing nitrate from groundwater and coking wastewater effluent.
Metal-encapsulated and nitrogen-doped carbon-based (M@NC) catalysts have emerged as promising options for electrochemical nitrate reduction reaction (ENRR) because of their excellent activity and stability. However, in the form of powder or the self-supporting metal nanoparticle-embedded carbon layer morphology, they show unsatisfactory denitrification performance when ENRR is performed at a high current density (e.g., >10 mA cm(-2)). In this work, we comprehensively determined the underlying reasons for this phenomenon and accordingly synthesized a free-standing M@NCNT (carbon nanotube) array on carbon cloth (CC) to resolve the issue. Experimental results show that the utilization efficiency of the active sites of M@NC plays a crucial role in guaranteeing superior ENRR activity under kinetically promoted conditions. Compared with the lying-down morphology, the unique standing-up structure enables more active centers that are accessible to the reactants, thus improving their utilization and overall ENRR performance. The as-prepared Co@NCNT/CC cathode delivered outstanding denitrification activity (with a removal proportion of nearly 100% over 3 h electrolysis at 10 mA cm(-2)) and good stability (continuously running for ENRR over 30 consecutive cycles without performance deterioration). When operated under the constant-current mode, it was also effective in removing nitrate from groundwater and real coking wastewater effluent. The findings provide important insights into the rational design of advanced M@NC catalysts toward ENRR.
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