4.8 Article

Revealing Nanoscale Chemical Heterogeneities in Polycrystalline Mo-BiVO4 Thin Films

期刊

SMALL
卷 16, 期 35, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202001600

关键词

bismuth vanadate; chemical heterogeneity; first principles; scanning X-ray microscopy; water splitting

资金

  1. Laboratory Directed Research and Development Program of Lawrence Berkeley National Laboratory under U.S. Department of Energy [DE-AC02-05CH11231]
  2. U.S. DOE Office of Science User Facility [DE-AC02-05CH11231]
  3. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  4. Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub
  5. Office of Science of the U.S. Department of Energy [DE-SC0004993]
  6. Deutsche Forschungsgemein-schaft (DFG, German Research Foundation) [428591260]
  7. DGI-UNAB Regular Grant [DI-21-18/REG]
  8. FONDECYT Iniciacion en Investigacion [11180590]
  9. DFG under Germany's Excellence Strategy [EXC 2089/1 - 390776260]

向作者/读者索取更多资源

The activity of polycrystalline thin film photoelectrodes is impacted by local variations of the material properties due to the exposure of different crystal facets and the presence of grain/domain boundaries. Here a multi-modal approach is applied to correlate nanoscale heterogeneities in chemical composition and electronic structure with nanoscale morphology in polycrystalline Mo-BiVO4. By using scanning transmission X-ray microscopy, the characteristic structure of polycrystalline film is used to disentangle the different X-ray absorption spectra corresponding to grain centers and grain boundaries. Comparing both spectra reveals phase segregation of V(2)O(5)at grain boundaries of Mo-BiVO(4)thin films, which is further supported by X-ray photoelectron spectroscopy and many-body density functional theory calculations. Theoretical calculations also enable to predict the X-ray absorption spectral fingerprint of polarons in Mo-BiVO4. After photo-electrochemical operation, the degraded Mo-BiVO(4)films show similar grain center and grain boundary spectra indicating V(2)O(5)dissolution in the course of the reaction. Overall, these findings provide valuable insights into the degradation mechanism and the impact of material heterogeneities on the material performance and stability of polycrystalline photoelectrodes.

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