CdS@Ni3(NO3)2(OH)4 nanorods@nanosheets for boosted photocatalytic H2 generation rate and stability under visible light irradiation

被引:1
|
作者
Yin, Xing-Liang [1 ]
Li, Lei-Lei [1 ]
Li, Xin-Yue [1 ]
Xue, Jia [1 ]
Zhao, Hai-Tao [1 ]
Shang, Qian-Qian [1 ]
Dou, Jian-Min [1 ]
机构
[1] Liaocheng Univ, Shandong Prov Key Lab Chem Energy Storage & Novel, Sch Chem & Chem Engn, Liaocheng 252059, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; H-2; generation; Core@shell heterostructures; Cadmium sulfide; Visible light; HYDROGEN EVOLUTION; MORPHOLOGY;
D O I
10.1016/j.colsurfa.2022.128352
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
H-2 generation from solar-driven water splitting has attracted significant interest and has promising to be applied. However, it is still a great challenge in terms of how to fabricate efficient photocatalyst by employing a low-cost and green approach. Herein, we report a novel core@shell heterostructure CdS@Ni-3(NO3)(2)(OH)(4) that was synthesized by using a facile solvothermal approach without any stabilizer usage. In this structure, the 2D Ni-3(NO3)(2)(OH)(4) nanosheet shell was intimately grown on the outside of 1D CdS nanorod core. This unique structure not only shortens and broadens the charge transfer path from interior to surface but also promotes charge separation and transportation across interfaces. In addition, the Ni-3(NO3)(2)(OH)(4) can prohibit CdS from photo and chemical corrosion to some degree. As a result, the optimized CdS@Ni-3(NO3)(2)(OH)(4) heterostructure exhibits an H-2 generation rate of 26.82 mmol g(-1) h(-1) much higher than that of pristine CdS (26.82 vs. 0.35 mmol g(-1) h(-1)) while maintaining long-term stability with no obvious deterioration of photocatalytic activity in 20 h reaction.
引用
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页数:7
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