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dc.contributor.authorIesalnieks, Mairis
dc.contributor.authorVanags, Mārtiņš
dc.contributor.authorAlsiņa, Linda Laima
dc.contributor.authorEglītis, Raivis
dc.contributor.authorGrīnberga, Līga
dc.contributor.authorSherrell, Peter C.
dc.contributor.authorŠutka, Andris
dc.date.accessioned2025-01-08T17:21:02Z
dc.date.available2025-01-08T17:21:02Z
dc.date.issued2024
dc.identifier.issn2198-3844
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/advs.202401261
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/67214
dc.descriptionThe authors acknowledge support from the Latvian national research program Project No. VPP-EM-FOTONIKA-2022/1-0001 Smart Materials, Photonics, Technologies and Engineering Ecosystems. P.C.S. acknowledges support from RMIT University through the RMIT Vice\u2010Chancellor's Research Fellowship scheme (2023). The European Union’s Horizon 2020 Framework Program H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2.en_US
dc.description.abstractWater electrolysis remains a key component in the societal transition to green energy. Membrane electrolyzers are the state-of-the-art technology for water electrolysis, relying on 80 °C operation in highly alkaline electrolytes, which is undesirable for many of the myriad end-use cases for electrolytic water splitting. Herein, an alternative water electrolysis process, decoupled electrolysis, is described which performed in mild acidic conditions with excellent efficiencies. Decoupled electrolysis sequentially performs the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER), at the same catalyst. Here, H+ ions generated from the OER are stored through pseudocapacitive (redox) charge storage, and released to drive the HER. Here, decoupled electrolysis is demonstrated using cheap, abundant, TiO2 for the first time. To achieve decoupled acid electrolysis, ultra-small anatase TiO2 particles (4.5 nm diameter) are prepared. These ultra-small TiO2 particles supported on a carbon felt electrode show a highly electrochemical surface area with a capacitance of 375 F g−1. When these electrodes are tested for decoupled water splitting an overall energy efficiency of 52.4% is observed, with excellent stability over 3000 cycles of testing. This technology can provide a viable alternative to membrane electrolyzers—eliminating the need for highly alkaline electrolytes and elevated temperatures. © 2024 The Authors. Advanced Science published by Wiley-VCH GmbH. --//-- This is an open-access article M. Iesalnieks, M. Vanags, L. L. Alsiņa, R. Eglītis, L. Grīnberga, P. C. Sherrell, A. Šutka, Efficient Decoupled Electrolytic Water Splitting in Acid through Pseudocapacitive TiO2. Adv. Sci. 2024, 11, 2401261. https://doi.org/10.1002/advs.202401261 published under the CC BY licence.en_US
dc.description.sponsorshipLatvian National Research Program Project No. VPP-EM-FOTONIKA-2022/1-0001; European Union’s Horizon 2020 Framework Program H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2.en_US
dc.language.isoengen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/739508/EU/Centre of Advanced Material Research and Technology Transfer/CAMART²en_US
dc.relation.ispartofseriesAdvanced Science;11 (28); 2401261
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Physicsen_US
dc.subjectelectrolysisen_US
dc.subjectpseudocapacitorsen_US
dc.subjecttitanium dioxideen_US
dc.titleEfficient Decoupled Electrolytic Water Splitting in Acid through Pseudocapacitive TiO2en_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.identifier.doi10.1002/advs.202401261


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