Abstract
Improved photocatalytic activities in highly ordered porous photocatalysts are often attributed to the larger surface area, higher light absorption, and suppressed charge recombination. Other underlying reasons for the improved charge transport, however, remain elusive at this stage. Herein, 3DOM BiVO4 photocatalysts are examined to understand the carrier dynamics and their effects in photocatalytic water splitting. Quantum confinement arising from the ultrathin and crystalline wall upshifted its conduction band, enabling photocatalytic proton reduction to hydrogen gas under visible-light illumination. Time-resolved microwave conductivity spectroscopy reveals its ∼6 times higher charge mobility and longer charge diffusion length relative to the bulk counterpart. The long lifetime (∼360 ns) of 3DOM BiVO4 with a power-law decay suggests the improved charge separation and the formation of shallow trapping states.
Original language | English (US) |
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Pages (from-to) | 3400-3407 |
Number of pages | 8 |
Journal | ACS Energy Letters |
Volume | 6 |
Issue number | 10 |
DOIs | |
State | Published - Oct 8 2021 |
Bibliographical note
Publisher Copyright:© 2021 American Chemical Society.
ASJC Scopus subject areas
- Chemistry (miscellaneous)
- Renewable Energy, Sustainability and the Environment
- Fuel Technology
- Energy Engineering and Power Technology
- Materials Chemistry