Abstract
Conventional photoelectrodes have shown dominantly single-signal photoelectrochemical (PEC) performance under reverse-bias, where only photo-generated minority carriers are involved in water splitting reactions. The extraordinary dynamic-mode operation of PEC water splitting is suggested herein, using the heterophasic copper indium selenide (CIS) with coexisting p- and n-type phases. CIS photoelectrodes with an interleaved p-n blended structure generate substantial photocathodic/-anodic currents resulting in transient spikes followed by saturation at negative/positive potential under light illumination. Then, the interleaved inner-depletions function as the charge transport pathway. Pulsed-bias (0 and 0.8 V vs. reversible hydrogen electrode) with a suitable frequency applied to the p-n blended CIS photoelectrodes under steady light illumination results in an extremely high photocurrent density of approximately 25 mA/cm2 (spike) and 10 mA/cm2 (saturation). Furthermore, the pulse-driven PEC operation shows remarkably high hydrogen evolution efficiency by suppressing the formation of large-size cluster bubbles and an intrinsic electric double layer.
Original language | English |
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Article number | 119839 |
Journal | Applied Catalysis B: Environmental |
Volume | 285 |
DOIs | |
State | Published - 15 May 2021 |
Keywords
- Biphasic
- Cu-In-Se
- Hydrogen
- Photoelectrochemical
- Pulse-driven