4.8 Article

Understanding and Controlling the Performance-Limiting Steps of Catalyst-Modified Semiconductors

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 12, Issue 1, Pages 199-203

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.0c02386

Keywords

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Funding

  1. National Science Foundation [1653982]
  2. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0021186]
  3. Camille Dreyfus TeacherScholar Awards Program
  4. IGERTSUN fellowship - National Science Foundation [1144616]
  5. Phoenix Chapter of the ARCS Foundation
  6. U.S. Department of Energy (DOE) [DE-SC0021186] Funding Source: U.S. Department of Energy (DOE)
  7. Direct For Mathematical & Physical Scien
  8. Division Of Chemistry [1653982] Funding Source: National Science Foundation

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Understanding and controlling factors that restrict the rates of fuel-forming reactions are crucial for designing effective catalyst-modified semiconductors for solar-to-fuel applications. This study reveals two distinct mechanisms of photoelectrochemical hydrogen production and highlights diagnostic tools for better understanding these processes. The complex interplay between transport of photons, electrons, and chemical substrates in photoelectrosynthetic reactions is illustrated in this work.
Understanding and controlling factors that restrict the rates of fuel-forming reactions are essential to designing effective catalyst-modified semiconductors for applications in solar-to-fuel technologies. Herein, we describe GaAs semiconductors featuring a polymeric coating that contains cobaloxime-type catalysts for photoelectrochemically powering hydrogen production. The activities of these electrodes (limiting current densities >20 mA cm(2) under 1-sun illumination) enable identification of fundamental performance-limiting bottlenecks encountered at relatively high rates of fuel formation. Experiments conducted under varying bias potential, pH, illumination intensity, and scan rate reveal two distinct mechanisms of photoelectrochemical hydrogen production. At relatively low polarization and pH, the limiting photoactivity is independent of illumination conditions and is attributed to a mechanism involving reduction of substrate protons. At relatively high polarization or pH, the limiting photoactivity shows a linear response to increasing photon flux and is attributed to a mechanism involving reduction of substrate water. This work illustrates the complex interplay between transport of photons, electrons, and chemical substrates in photoelectrosynthetic reactions and highlights diagnostic tools for better understanding these processes.

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