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Oriented ZnmIn2Sm+3@In2S3 heterojunction with hierarchical structure for efficient photocatalytic hydrogen evolution.
- Source :
-
Applied Catalysis B: Environmental . May2019, Vol. 244, p604-611. 8p. - Publication Year :
- 2019
-
Abstract
- Graphical abstract Highlights • A novel J-J type Zn m In 2 S m+3 @In 2 S 3 heterojunction was designed based on conductive anisotropy. • The J-J type heterojunction was fabricated with the assistance of oxalic acid. • The heterojunction improves the carrier separation efficiency and extends light response range. • The heterojunction exhibits significantly enhanced photocatalytic H 2 evolution activity. Abstract It remains a great challenge to design and prepare highly efficient semiconductor-based photocatalysts for water splitting. To achieve this goal, the design of oriented heterojunctions for efficient carrier transport and separation is a new strategy based on their conductive anisotropy. Herein, a novel oriented J-J type Zn m In 2 S m+3 @In 2 S 3 heterojunction photocatalyst with hierarchical structures is fabricated with the assistance of oxalic acid. The hierarchical structures consist of 'flower-like' hollow Zn m In 2 S m+3 microspheres with epitaxially grown quantum confined In 2 S 3 along the petal rims (J-J type heterojunction). This heterojunction improves the transport and separation of the photoexcited carriers, and extends the visible-light response range. Thus, the heterojunction photocatalyst exhibits significantly enhanced photocatalytic activity with a hydrogen evolution rate of 330 μmol h−1, which is about 4 times higher than that of single ZnIn 2 S 4. The findings provide new insights to construct efficient oriented heterojunctions for anisotropic semiconductors. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09263373
- Volume :
- 244
- Database :
- Academic Search Index
- Journal :
- Applied Catalysis B: Environmental
- Publication Type :
- Academic Journal
- Accession number :
- 134226510
- Full Text :
- https://doi.org/10.1016/j.apcatb.2018.11.088