Boosting photothermal CO2 hydrogenation with H2O by MIL-100(Fe) derived Fe@C confined Ni2P

被引:5
|
作者
Zhu, Pengfei [1 ]
Geng, Mengrong [1 ]
Qin, Shuang [1 ]
Cao, Heyang [1 ]
He, Zhenhong [2 ]
Gao, Xinhua [3 ]
Wang, Chuanyi [1 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Environm Sci & Engn, Xian 710021, Peoples R China
[2] Shaanxi Univ Sci & Technol, Sch Chem & Chem Engn, Xian 710021, Peoples R China
[3] Ningxia Univ, Coll Chem & Chem Engn, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
Photothermal catalysis; MOFs; CO; 2; conversion; C; H; 6; production; PHOTOCATALYST; REDUCTION; NANOSHEET; REMOVAL; ARRAYS;
D O I
10.1016/j.surfin.2024.104032
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 conversion of CO2 into chemical products or fuels of great value always remains an outstanding challenge. Here, we report a heterojunction Fe@C/Ni2P composite catalyst obtained by preparing MIL-100(Fe) derived Fe@C confined Ni2P nanoparticles, which is applied to photothermal catalytic CO2 hydrogenation with H2O. Without adding any sacrificial agents or co-catalysts, the optimal Fe@C/Ni2P sample shows higher yields for CO2-to-C2H6 and CO2-to-CO yield of 5.83 mu mol g- 1h- 1 and 179.9 mu mol g-1 h-1 than that of pristine Fe@C and Ni2P, respectively. The experimental results indicated that the obtained Fe@C/Ni2P can act as catalytic sites to adsorb, activate, and convert CO2 under low-intensity LED light irradiation (420 nm) with a temperature of 200 degrees C. The physical structure, photochemical properties and energy band structure of the Fe@C/Ni2P composite catalysts were investigated by XRD, XPS, FT-IR, TEM, BET, respectively. Furthermore, the reaction pathway of Fe@C/Ni2P photothermal catalytic CO2 hydrogenation with H2O to C2 products and CO were systematically analyzed by in situ infrared spectroscopy (DRIFTS).
引用
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页数:10
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