Spinel-Type Mixed Metal Sulfide NiCo2S4 for Efficient Photocatalytic Reduction of CO2 with Visible Light

被引:31
|
作者
Xiong, Zhuang [1 ]
Huang, Lijuan [1 ]
Peng, Junwen [1 ]
Hou, Yidong [1 ]
Ding, Zhengxin [1 ]
Wang, Sibo [1 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; reduction; metal sulfides; NiCo2S4; photocatalysis; spinel; ARTIFICIAL PHOTOSYNTHETIC SYSTEMS; BINUCLEAR RUTHENIUM(II) COMPLEX; GRAPHITIC CARBON NITRIDE; ORGANIC FRAMEWORKS; HYDROGEN EVOLUTION; COCATALYST; SEMICONDUCTORS; NANOPARTICLES; PERFORMANCE; NANOSHEETS;
D O I
10.1002/cctc.201901379
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
Mixed metal oxides with a spinel structure have exhibited great opportunities for photocatalytic CO2 reduction; however, the abilities of their sulfide counterparts in this promising area are much less reported. Herein, we demonstrate the synthesis of a ternary metal sulfide, namely NiCo2S4, and its first application to catalyze the CO2 photoreduction reaction under visible light irradiation. The NiCo2S4 material is prepared through a coupled solvothermal-ion exchange strategy, and is fully checked by diverse characterizations, including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDX) and N-2 sorption measurements. Under visible light irradiation in a classic tandem photochemical system, this non-noble-metal NiCo2S4 catalyst affords a considerable activity and high stability for CO2 deoxygenative reduction, delivering a high CO-liberating rate of 43.5 mu mol mg(-1) h(-1). The in-situ PL and transient photocurrent measurements reveal that the spinel catalyst can hamper recombination and accelerate transfer of light-excited charge carriers, and thus boosting the CO2 reduction reaction. At last, a possible mechanism of the NiCo2S4-catalyzed CO2 photoreduction reaction is proposed.
引用
收藏
页码:5513 / 5518
页数:6
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