4.7 Article

Amorphous iron (III)-borate decorated electrochemically treated-BiVO4 photoanode for efficient photoelectrochemical water splitting

期刊

CHEMICAL ENGINEERING JOURNAL
卷 411, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128480

关键词

Bismuth vanadate; Amorphous iron (III)-borate co-catalysts; 10 s- electrochemical treatment; Oxygen vacancies; Photoelectrochemical water splitting

资金

  1. Natural Science Foundation of Jiangsu Province [SBK2017041090]
  2. National Natural Science Foundation of China [61674071, 21878129]
  3. Youth Foundation of Jiangsu Scientific Committee [BK20170531]
  4. Industry Prospect and Key Core Technology (Competition Project) of Jiangsu Province [BE2019093]

向作者/读者索取更多资源

The decoration of FeBi co-catalyst on the surface of BiVO4 significantly enhances the PEC water splitting performance, offering a new route for efficient solar-to-hydrogen conversion. The FeBi/E-BiVO4 heterostructure exposed more active sites and rich oxygen vacancies, leading to improved charges transfer and separation efficiencies, contributing to the increased ABPE up to 1.35%.
BiVO4 has attracted widespread attention as a promising semiconductor material for recent year. However, poor water oxidation kinetics and severe surface charge recombination are still the bottlenecks, which significantly hinders the practical solar-to-hydrogen conversion. In this work, we successfully decorated iron-borate (FeBi) co catalyst on the surface of electrochemical treated-BiVO4 (E-BVO, via 10 s), and the obtained FeBi/E-BiVO4 heterostructure drastically enhances the PEC water splitting performance. The optimal sample exhibits an excellent photocurrent density of 3.24 mA/cm(2) at 1.23 VRHE, a 600% increase over the pristine BiVO4 (0.46 mA/cm(2)). The applied bias photo-to-current efficiency (ABPE) has been increased up to 1.35%, since FeBi co-catalyst and E-BVO contributes to expose more active sites and offer rich oxygen vacancies, respectively, which efficiently boosted the charges transfer and separation efficiencies. Therefore, this work will provide an alternative route to realize the efficient solar-to-hydrogen conversion.

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