4.7 Article

In Situ Construction of Direct Z-Scheme CsxWO3/CsPbBr3 Heterojunctions via Cosharing Cs Atom

Journal

SOLAR RRL
Volume 5, Issue 5, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/solr.202100036

Keywords

cosharing atoms; CsPbBr3; CsxWO3; in situ constructions; Z-schemes

Funding

  1. National Natural Science Foundation of China [21875288]
  2. GDUPS
  3. NSF of Guangdong Province [2019B151520050]
  4. Fundamental Research Funds for the Central Universities [19lgjc07, 19lgzd24]

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By cosharing Cs atoms and in situ growing CsPbBr3 nanoparticles on the surface of CsxWO3 nanorods, high-quality interface with strong interaction is successfully constructed, forming a direct Z-scheme charge transfer pathway for effective separation of photogenerated carriers and enhancement of photocatalytic hydrogen production performance.
To make full use of solar energy and achieve effective separation of photogenerated carriers, semiconductor heterojunction engineering is becoming increasingly significant nowadays. Herein, CsxWO3 /CsPbBr3 heterojunctions via cosharing the Cs atom are synthesized by a facile acid solution method, which involves the in situ growth of CsPbBr3 nanoparticles on the surface of CsxWO3 nanorods. Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) tests confirm that a high-quality interface with strong interaction between CsxWO3 and CsPbBr3 is constructed successfully. Thus, a direct Z-scheme charge transfer pathway is built in such close-contact heterojunctions, which can not only effectively prevent the recombination of photogenerated carriers, but also preserve the carriers with higher redox abilities, as confirmed by electron spin resonance (ESR) as well as Kelvin probe force microscopy (KPFM). As a proof of concept, the photocatalytic hydrogen production performance of CsxWO3 /CsPbBr3 is evaluated in ethyl acetate, and a 17-fold enhancement in hydrogen production rate as compared with pristine CsxWO3 is obtained, verifying the effective charge separation in such heterojunctions. Herein, a new idea for in situ synthesis of high-quality perovskite-based heterojunctions is provided, which will broaden their optoelectrical applications.

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