Controllable synthesis of inorganic-organic Zn1-xCdxS-DETA solid solution nanoflowers and their enhanced visible-light photocatalytic hydrogen-production performance

被引:46
|
作者
Lv, Jiali [1 ,2 ,3 ,4 ]
Zhang, Jinfeng [1 ]
Dai, Kai [1 ]
Liang, Changhao [1 ,2 ,3 ]
Zhu, Guangping [1 ]
Wang, Zhongliao [1 ]
Li, Zhen [1 ]
机构
[1] Huaibei Normal Univ, Anhui Key Lab Energet Mat, Coll Phys & Elect Informat, Huaibei 235000, Peoples R China
[2] Chinese Acad Sci, Hefei Inst Phys Sci, Key Lab Mat Phys, Hefei 230031, Anhui, Peoples R China
[3] Chinese Acad Sci, Hefei Inst Phys Sci, Anhui Key Lab Nanomat & Nanotechnol, Hefei 230031, Anhui, Peoples R China
[4] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTRON-TRANSFER; CATION-EXCHANGE; METAL SULFIDE; EFFICIENT; WATER; TIO2; GENERATION; NANOSHEETS; EVOLUTION; H-2;
D O I
10.1039/c7dt01892d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Sustainable photocatalytic hydrogen evolution (PHE) of water splitting has been utilized to solve the serious environmental pollution and energy shortage problems over the last decade. Inorganic-organic hybrid materials could combine the organic molecules and functional inorganic blocks into unique materials through complicated physical and chemical interactions. In this paper, diethylenetriamine (DETA) was used as an organic molecule template for the synthesis of inorganic-organic Zn1-xCdxS-DETA solid solution nanoflowers (NFs) at very low temperature. The obtained Zn0.2Cd0.8S-DETA NFs exhibited the highest H-2 production rate (12 718 mu mol g(-1) h(-1)), which is 1.75 times as high as that of CdS-DETA. The suitable conduction band potential and excellent visible-light absorption of Zn0.2Cd0.8S-DETA solid solution NFs are closely related to the excellent PHE activity. Furthermore, the calculation on the electronic structure provides a new understanding of the band-gap shifts of the Zn1-xCdxS-DETA solid solution hybrids and the design of novel structural photocatalysts.
引用
收藏
页码:11335 / 11343
页数:9
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