Cobalt nanoparticles encapsulated in porous nitrogen-doped carbon: Oxygen activation and efficient catalytic removal of formaldehyde at room temperature

被引:74
作者
Zhu, Dandan [1 ,2 ]
Huang, Yu [2 ,3 ]
Cao, Jun-ji [2 ,3 ]
Lee, Shun Cheng [4 ]
Chen, Meijuan [5 ]
Shen, Zhenxing [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Dept Environm Sci & Engn, Xian 710049, Shaanxi, Peoples R China
[2] Chinese Acad Sci, Inst Earth Environm, SKLLQG, Key Lab Aerosol Chem & Phys, Xian 710049, Shaanxi, Peoples R China
[3] CAS Ctr Excellence Quaternary Sci & Global Change, Xian 710061, Shaanxi, Peoples R China
[4] Hong Kong Polytech Univ, Dept Civil & Environm Engn, Hong Kong, Peoples R China
[5] Xi An Jiao Tong Univ, Sch Human Settlements & Civil Engn, Xian 710049, Shaanxi, Peoples R China
基金
美国国家科学基金会;
关键词
Metallic Co nanoparticles; Porous nitrogen-doped carbon; HCHO removal; Catalytic oxidation; INDOOR FORMALDEHYDE; MANGANESE OXIDE; HCHO OXIDATION; PERFORMANCE; PT/TIO2; SURFACE; MNO2; MECHANISM; NANORODS;
D O I
10.1016/j.apcatb.2019.117981
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
The removal of carcinogenic formaldehyde (HCHO) to improve indoor air quality has attracted significant attention. Designing efficient catalysts for practical HCHO oxidation without use of noble metals remains challenging. In this study, metallic Co nanoparticles were encapsulated with porous nitrogen-doped carbon (Co@NC). This catalyst achieved HCHO elimination at room temperature for the first time. The as-prepared Co@NC catalyst exhibited superior catalytic activity (> 80%) for HCHO removal compared with the oxidized one, and possessed the excellent stability. Theoretical calculations showed that the metallic Co in Co@NC is the active site for O-2 dissociation, which enhanced the catalytic activity compared to traditional transition-metal oxides, such as Co3O4 with the high-valence state Co3+ providing active sites. The formate species was the main intermediate, which was further oxidized to CO2 as the final product. Hence, an efficient non-noble-metal catalyst for room-temperature HCHO oxidation was developed.
引用
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页数:8
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