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Bifunctional Perovskite‐BiVO 4 Tandem Devices for Uninterrupted Solar and Electrocatalytic Water Splitting Cycles
Author(s) -
Pornrungroj Cha,
Andrei Virgil,
Rahaman Motiar,
Uswachoke Chawit,
Joyce Hannah J.,
Wright Dominic S.,
Reisner Erwin
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202008182
Subject(s) - materials science , tandem , perovskite (structure) , electrolysis , bifunctional , semiconductor , water splitting , electrolysis of water , optoelectronics , chemical engineering , catalysis , electrode , photocatalysis , composite material , chemistry , biochemistry , engineering , electrolyte
Photoelectrochemical (PEC) fuel synthesis depends on the intermittent solar intensity of the diurnal cycle and ceases at night. Here, an integrated device that does not only possess PEC water splitting functionality, but also operates as an electrolyzer in the nocturnal period to improve the overall capacity factor is described. The bifunctional system is based on an “artificial leaf” tandem PEC architecture that contains an inverse‐structure lead halide perovskite protected by a graphite epoxy/parylene‐C coating (conferring 96 h stability of operation in water), and a porous BiVO 4 semiconductor. The light‐absorbers are interfaced with a H 2 evolution catalyst (Pt) and a Co‐based water oxidation catalyst, respectively, which can also be directly driven by electricity. Thus, the device can operate in PEC mode during irradiation and switch to an electricity‐powered mode in the dark through bypassing of the semiconductor configuration. The bifunctional perovskite‐BiVO 4 tandem provides a solar‐to‐hydrogen efficiency of 1.3% under simulated solar irradiation and an onset for water electrolysis at 1.8 V. The compact design and low cost of the proposed device may provide an advantage over other technologies for round‐the‐clock fuel production.