Abstract
Highly efficient and direct photocatalytic H2 evolution from water splitting is a hopeful route to convert solar energy into renewable and storable chemical energy. However, it's still a challenging task to eliminate the constraint of sacrificial agents. Herein, by integrating the architecture guidance and energy band engineering into the design conception, a novel CdS@Ti3C2@CoO hierarchical tandem p-n heterojunction photocatalytic system is designed and prepared for the first time. Ti3C2 nanosheets not only solve the compatibility problem between CdS and CoO but also function as a bridge to consolidate them into a special tandem p-n heterojunction where two secondary internal electric fields are set up and combined into the strong internal electric field existing in the p-n heterojunction. The triple-internal electric field can dramatically boost the separation efficiency of photogenerated charge carriers and realize the regulation of their spatial motion. This specific photocatalytic system exhibits superior photocatalytic performance with a H2 evolution activity of 134.46 μmol·h−1·g−1 and excellent stability without any sacrificial agents. Our work introduces a potential avenue to design efficient photocatalysts by constructing multi-hierarchical systems toward practical application in solar energy conversion.
Original language | English (US) |
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Article number | 123130 |
Journal | Chemical Engineering Journal |
Volume | 383 |
DOIs | |
State | Published - Mar 1 2020 |
Keywords
- H evolution
- Hierarchical tandem p-n heterojunction
- Spatial motion
- Triple-internal electric field
ASJC Scopus subject areas
- General Chemistry
- Environmental Chemistry
- General Chemical Engineering
- Industrial and Manufacturing Engineering