Unraveling the Mechanisms of Beneficial Cu-Doping of NiO-Based Photocathodes.

J Phys Chem C Nanomater Interfaces

PhotoCatalytic Synthesis Group, MESA+ Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.

Published: July 2021

Dye-sensitized photoelectrochemical (DSPEC) water splitting is an attractive approach to convert and store solar energy into chemical bonds. However, the solar conversion efficiency of a DSPEC cell is typically low due to a poor performance of the photocathode. Here, we demonstrate that Cu-doping improves the performance of a functionalized NiO-based photocathode significantly. Femtosecond transient absorption experiments show longer-lived photoinduced charge separation for the Cu:NiO-based photocathode relative to the undoped analogue. We present a photophysical model that distinguishes between surface and bulk charge recombination, with the first process (∼10 ps) occurring more than 1 order of magnitude faster than the latter. The longer-lived photoinduced charge separation in the Cu:NiO-based photocathode likely originates from less dominant surface recombination and an increased probability for holes to escape into the bulk and to be transported to the electrical contact of the photocathode. Cu-doping of NiO shows promise to suppress detrimental surface charge recombination and to realize more efficient photocathodes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8411848PMC
http://dx.doi.org/10.1021/acs.jpcc.1c03553DOI Listing

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