4.7 Article

Reinforcement of Visible-Light Harvesting and Charge-Transfer Dynamics of BiVO4 Photoanode via Formation of p-n Heterojunction with CuO for Efficient Photoelectrocatalytic Water Splitting

期刊

ACS APPLIED ENERGY MATERIALS
卷 5, 期 6, 页码 6618-6632

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c04120

关键词

bismuth vanadate; copper oxide; p-n heterojunction; charge separation; interfacial charge transfer; photoelectrocatalysis

资金

  1. DST-Technology Mission Division, New Delhi through Hydrogen and Fuel Cell (HFC) -2018 Scheme [DST/TMD/HFC/2K18/101]
  2. DST-INSPIRE Fellowship [IF170764]

向作者/读者索取更多资源

By loading copper oxide onto the surface of bismuth vanadate to form a p-n junction, the light absorption capacity, charge transfer rate, and separation of electron-hole pairs were effectively improved, leading to enhanced efficiency in the photoelectrocatalytic water oxidation process.
High photoinduced charge recombination process and indolent water oxidation kinetics are major drawbacks of the bismuth vanadate (BiVO4) photoanode in photoelectrocatalytic (PEC) water splitting. To address these issues, a bismuth vanadate/copper oxide (BiVO4/CuO) p-n junction electrode was fabricated via the electrodeposition method, and its PEC performance was studied using 0.1 M potassium phosphate (KPi) as an electrolyte under AM 1.5G (100 mW cm(-2)) irradiation. At an optimized condition, the BiVO4/CuO p-n junction electrode showed improvement in the current density of 2.05 mA cm(-2) at +1.23 V-RHE, which was similar to 2-fold higher than the BiVO4 electrode (0.99 mA cm(-2)). The applied bias photon-to-current efficiency (ABPE) of the BiVO4/CuO electrode was also similar to 2.5-fold higher than the BiVO4 electrode. Loading of CuO over the BiVO4 surface improved the light absorption ability of the electrode in the entire UV-vis region, leading to generation of a greater number of photoinduced charge carriers, and it also enhanced the reactive sites for water oxidation as per the calculation of double-layer capacitance (C-dl). The formation of inner electric field (IEF) at the interface between BiVO4 and CuO offered well-separated electron-hole pairs in association with improvement in the lifetime of charge carriers, and as a consequence, the BiVO4/CuO electrode showed a transient decay time of 4.45 s, which was similar to 1.6-fold higher than the BiVO4 electrode (2.81 s). The formation of p-n junction between BiVO4 and CuO significantly reduced the charge transfer resistance (R-ct) at the electrode/electrolyte interface (EEI), and as a result, the BiVO4 and BiVO4/CuO electrodes show R-ct values of 454.4 and 201.9 Omega, respectively, under light illumination. Moreover, the Bode phase analysis confirmed quick hole consumption in the presence of the BiVO4/CuO electrode over the pristine BiVO4 electrode during water oxidation process. Overall, the formation of a p-n junction facilitated well-separated electron-hole pairs and improved the hole transfer at the EEI for an efficient PEC water oxidation process.

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