Understanding and Controlling the Performance-Limiting Steps of Catalyst-Modified Semiconductors
Author(s) -
Nghi P. Nguyen,
Brian L. Wadsworth,
Daiki Nishiori,
Edgar A. Reyes Cruz,
Gary F. Moore
Publication year - 2020
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.0c02386
Subject(s) - semiconductor , limiting , polarization (electrochemistry) , catalysis , materials science , hydrogen production , hydrogen , substrate (aquarium) , photon , limiting current , solar fuel , optoelectronics , nanotechnology , chemical physics , chemical engineering , photocatalysis , electrode , chemistry , optics , electrochemistry , physics , mechanical engineering , biochemistry , oceanography , organic chemistry , engineering , geology
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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