Nanodenitrification with bimetallic nanoparticles confined in N-doped mesoporous carbon

被引:40
|
作者
Wang, Jing [1 ]
Teng, Wei [1 ]
Ling, Lan [1 ]
Fan, Jianwei [1 ]
Zhang, Wei-xian [1 ]
Deng, Zilong [1 ]
机构
[1] Tongji Univ, Sch Environm Sci & Engn, State Key Lab Pollut Control, 1239 Siping Rd, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; NITRATE REDUCTION; OXYGEN REDUCTION; ELECTROCATALYTIC REDUCTION; CATALYTIC-REDUCTION; ENHANCED ACTIVITY; WATER; EFFICIENT; PERSPECTIVES; REGENERATION;
D O I
10.1039/d0en00087f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nitrate and phosphorous contamination owing to increasing fossil fuel consumption and the use of modern fertilizers is the leading cause of the eutrophication and deterioration of water quality worldwide. Herein, we introduced an N-doped ordered mesoporous carbon-based skeleton with Cu-Pd nanocrystals (Cu-Pd@N-OMC) for the electrocatalytic reduction of NO3- to dinitrogen (N-2). Laboratory experiments demonstrated high NO3- removal (91%) and N-2 selectivity (97%) for eutrophic water treatment. The nanocatalyst also remained highly active over 15 experimental cycles. Metal-organic frameworks (MOFs) induced dispersion and the embedment of small Cu-Pd nanocrystals (4-9 nm) in the carbon mesochannels. Moreover, the metal loading was as low as 5 wt% with the Cu/Pd ratio at 4/1. The results suggested that the electrocatalytic reactivity could be fine-tuned by the size and crystallinity of the Cu-Pd nanoparticles through controlling the pyrolysis temperature. The high-density Cu-Pd nanocrystals promoted rapid hydrogen adsorption to cleave the N-O bond for high N-2 selectivity. The incorporation of MOFs and OMC improved the dispersion and stabilization of metallic nanoparticles for prolonged electrocatalytic activity and durability.
引用
收藏
页码:1496 / 1506
页数:11
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