4.6 Article

Tuning Selectivity of Photoelectrochemical Water Oxidation via Facet-Engineered Interfacial Energetics

Journal

ACS ENERGY LETTERS
Volume 6, Issue 11, Pages 4071-4078

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.1c01831

Keywords

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Funding

  1. NSFC [22172077]
  2. Natural Science Foundation of Jiangsu Province of China [BK20211573]
  3. Jiangsu International Science and Technology Cooperation Program [BZ2020063]
  4. Fundamental Research Funds for the Central Universities [30921011216]
  5. National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2019R1A2C3010479, 2019M1A2A2065612, 2019R1A4A1029237]
  6. Yonsei-KIST Convergence Research Program

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Water oxidation kinetics is crucial for hydrogen production in solar water splitting, and the interface energetics formed by crystal facets can regulate product selectivity. The (010) facet of the BiVO4 photoanode can produce high-value hydrogen peroxide, improving the efficiency of applied bias photon-to-current in photoelectrochemical water splitting. This study reveals a new opportunity to enhance solar-to-hydrogen efficiency.
Water oxidation kinetics has been identified as the bottleneck of the solar water splitting reaction for H-2 production. Herein, we demonstrate that even for crystal facets with the same thermodynamically favorable pathway for water oxidation, the interfacial energetics formed by the terminated facet/electrolyte interface can significantly regulate the water oxidation kinetics to tune the product selectivity. Specifically, we elucidate that the (010) facet of the BiVO4 photoanode can offer suitable band bending and deep valence band level to produce high-value-added hydrogen peroxide (H2O2) with an average Faradaic efficiency of 70% from water oxidation. This simple strategy without other modifications can lead to a 30-fold increase in the applied bias photon-to-current efficiency of photoelectrochemical water splitting. This study sheds new light on the crystal facet effect beyond the erstwhile focus on charge separation and transfer and offers a new opportunity to enhance the solar-to-H-2 efficiency.

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