Sol-gel copper chromium delafossite thin films as stable oxide photocathodes for water splittingElectronic supplementary information (ESI) available: Experimental details, the UV-vis absorbance spectrum for an FTO/CuCrO2 electrode, an additional SEM image, linear scan voltammograms under transient 1 sun illumination and photocurrent transients under 1 sun illumination in 0.1 M HClO4, linear scan voltammograms under transient illumination in 0.1 M NaOH, and long-term chronoamperometric experiment
Significant effort is being devoted to the study of photoactive electrode materials for artificial photosynthesis devices. In this context, photocathodes promoting water reduction, based on earth-abundant elements and possessing stability under illumination, should be developed. Here, the photoelect...
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Zusammenfassung: | Significant effort is being devoted to the study of photoactive electrode materials for artificial photosynthesis devices. In this context, photocathodes promoting water reduction, based on earth-abundant elements and possessing stability under illumination, should be developed. Here, the photoelectrochemical behavior of CuCrO
2
sol-gel thin film electrodes prepared on conducting glass is presented. The material, whose direct band gap is 3.15 eV, apparently presents a remarkable stability in both alkaline and acidic media. In 0.1 M HClO
4
the material is significantly photoactive, with IPCE values at 350 nm and 0.36 V
vs.
RHE of over 6% for proton reduction and 23% for oxygen reduction. This response was obtained in the absence of charge extraction layers or co-catalysts, suggesting substantial room for optimization. The photocurrent onset potential is equal to 1.06 V
vs.
RHE in both alkaline and acidic media, which guarantees the combination of the material with different photoanodes such as Fe
2
O
3
or WO
3
, potentially yielding bias-free water splitting devices.
Sol-gel prepared copper chromium delafossite electrodes behave as stable and efficient photocathodes for water reduction without the need for co-catalysts. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c5ta05227k |