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Co-ZIF-derived dual Co and Co 3 S 4 nanoparticles encapsulated in N-doped carbon matrix for efficient photocatalytic CO 2 reduction
被引:2
作者:
Huang, Lili
[1
]
Mo, Shengpeng
[1
]
Zhao, Xin
[1
]
Zhou, Jiangjing
[1
]
Zhang, Yanan
[1
]
Zhou, Xiaobin
[1
]
Fan, Yinming
[1
]
Xie, Qinglin
[1
]
Ye, Daiqi
[2
]
机构:
[1] Guilin Univ Technol, Coll Environm Sci & Engn, Guilin 541004, Peoples R China
[2] South China Univ Technol, Sch Environm & Energy, Guangzhou 510006, Peoples R China
来源:
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING
|
2024年
/
12卷
/
03期
基金:
中国国家自然科学基金;
关键词:
Co-ZIF;
Dual nanoparticles;
N-doped carbon;
CO2;
photoreduction;
CATALYST;
GRAPHENE;
D O I:
10.1016/j.jece.2024.112566
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
In this study, a novel N -doped carbon -coated dual Co and Co 3 S 4 nanoparticles composite (Co-Co 3 S 4 @NC) has been developed by pyrolysis of an ideal flower-like Co-ZIF precursor followed via subsequent hydrothermal sulfidation. Under visible -light irradiation, the Co-Co 3 S 4 @NC exhibits outstanding performances for CO 2 reduction with H 2 O vapor into CO (23.14 mu mol g - 1 h -1 ) and CH 4 (0.62 mu mol g - 1 h -1 ) in a continuous flow system, significantly outperforming the single Co@NC photocatalyst. The experimental results demonstrate that the energy band structure in Co-Co 3 S 4 @NC can provide a more favorable reduction potential for the effective reduction of CO 2 . Moreover, the presence of Co 3 S 4 is beneficial for the rapid separation and transfer of charges, thereby enhancing the utilization of photogenerated charge carriers. Thanks to its unique composition, CoCo 3 S 4 @NC possesses abundant active sites for chemisorption and activation of CO 2 , which facilitates CO 2 photoreduction. The reaction mechanism is revealed in detail by analyzing the key intermediate species obtained through in situ DRIFTS. The current work offers a facile route for the construction of MOF-derived composites for promising photocatalytic reactions.
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页数:9
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