Abstract
This paper studies how electrochemically inserting or extracting lithium ions in TiO2 can trigger and orient solar hydrogen evolution reaction. LixTiO2 is envisioned as a photo(electro)catalyst, whose rejuvenation can be achieved by in situ potential control. The investigations are conducted in a half-battery cell design where a mesoporous, anatase TiO2 thin film (negative electrode candidate) is deposited onto a transparent conducting oxide (FTO) substrate, water-in-salt (WiSE) is used as an electrolyte. Changing the state of charge of the working electrode material, will adjust the ratio between the Li-rich phase (Li0.5TiO2 blue) and the Li-poor phase (Li0.01TiO2 uncolored), which will tune the opto-electronic properties of the material, potentially changing the light-matter interaction. The impact of light on the interplay between hydrogen evolution reaction and lithium insertion/extraction in TiO2 is investigated using classical electrochemical characterizations inspired from both battery and photoelectrode communities. With a minimum of Li-rich phase solar hydrogen is produced at the working or at the counter electrode while lithium in photo-extracted of the Li-rich phase to reform TiO2.
Graphical Abstract
Highlights
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Triggering the HER via a control of potential.
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Understanding the interplay between hydrogen evolution reaction and lithium insertion/extraction in TiO2 under light.
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Li-rich phase is photo(electro)chemical active in the visible range.
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Controlling in space, the localization of the HER.
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All data generated or analysed during this study are included in this published article [and its supplementary information files].
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JS thanks the ED397 from Sorbonne University for his Ph.D. grant.
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Sum, J., Krins, N. & Laberty-Robert, C. Li-ion insertion coupled solar HER. J Sol-Gel Sci Technol 107, 278–288 (2023). https://doi.org/10.1007/s10971-023-06122-w
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DOI: https://doi.org/10.1007/s10971-023-06122-w