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

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...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2017-08, Vol.46 (34), p.11335-11343
Hauptverfasser: Lv, Jiali, Zhang, Jinfeng, Dai, Kai, Liang, Changhao, Zhu, Guangping, Wang, Zhongliao, Li, Zhen
Format: Artikel
Sprache:eng
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Zusammenfassung: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 Zn 1− x Cd x S-DETA solid solution nanoflowers (NFs) at very low temperature. The obtained Zn 0.2 Cd 0.8 S-DETA NFs exhibited the highest H 2 production rate (12 718 μmol 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 Zn 0.2 Cd 0.8 S-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 Zn 1− x Cd x S-DETA solid solution hybrids and the design of novel structural photocatalysts. 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.
ISSN:1477-9226
1477-9234
DOI:10.1039/c7dt01892d