Pushing the limits in photosensitizer-catalyst interaction via a short cyanide bridge for water oxidation
buir.contributor.author | Ghobadi, Türkan Gamze Ulusoy | |
buir.contributor.author | Ghobadi, Amir | |
buir.contributor.author | Phul, Ruby | |
buir.contributor.author | Durgun, Engin | |
buir.contributor.author | Özbay, Ekmel | |
buir.contributor.author | Karadaş, Ferdi | |
buir.contributor.orcid | Ghobadi, Türkan Gamze Ulusoy|0000-0002-7669-1587 | |
buir.contributor.orcid | Phul, Ruby|0000-0003-3269-4951 | |
buir.contributor.orcid | Durgun, Engin|0000-0002-0639-5862 | |
buir.contributor.orcid | Özbay, Ekmel|0000-0003-2953-1828 | |
buir.contributor.orcid | Karadaş, Ferdi|0000-0001-7171-9889 | |
dc.citation.epage | 100319-16 | en_US |
dc.citation.issueNumber | 2 | en_US |
dc.citation.spage | 100319-1 | en_US |
dc.citation.volumeNumber | 2 | en_US |
dc.contributor.author | Ghobadi, Türkan Gamze Ulusoy | |
dc.contributor.author | Ghobadi, Amir | |
dc.contributor.author | Demirtaş, M. | |
dc.contributor.author | Phul, Ruby | |
dc.contributor.author | Yıldız, E. A. | |
dc.contributor.author | Yağlıoğlu, H. G. | |
dc.contributor.author | Durgun, Engin | |
dc.contributor.author | Özbay, Ekmel | |
dc.contributor.author | Karadaş, Ferdi | |
dc.date.accessioned | 2022-02-17T08:37:49Z | |
dc.date.available | 2022-02-17T08:37:49Z | |
dc.date.issued | 2021-02-24 | |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.description.abstract | The realization of high-performance, precious-metal-free, stable, and robust photoanodes for water oxidation is one of the bottlenecks for dye-sensitized water splitting. Herein, we integrate an organic photosensitizer, which absorbs visible light above 500 nm, with a Prussian blue (PB) network to sensitize a visible-light-absorbing semiconductor, WO3. Through comprehensive steady-state and ultrafast transient absorption studies, we show that the coupling of a photosensitizer to a catalyst through a short cyanide bridging group in a PB structure generates appropriate energy levels for an efficient charge transfer from the photosensitizer to the visible-light-absorbing semiconductor. The photoanode retains its structural integrity and high photoelectrochemical activity for at least 2 h of solar irradiation under mildly acidic conditions (pH 3), which reaches around 1.30 mA/cm2 at 1.23 VRHE. This work provides a simple recipe with a toolbox that can be extended to a variety of organic photosensitizers and semiconductors. | en_US |
dc.description.provenance | Submitted by Samet Emre (samet.emre@bilkent.edu.tr) on 2022-02-17T08:37:49Z No. of bitstreams: 1 Pushing_the_limits_in_photosensitizer-catalyst_interaction_via_a_short_cyanide_bridge_for_water_oxidation.pdf: 3932767 bytes, checksum: 8d8e05feedb86e5432ab8017a4713987 (MD5) | en |
dc.description.provenance | Made available in DSpace on 2022-02-17T08:37:49Z (GMT). No. of bitstreams: 1 Pushing_the_limits_in_photosensitizer-catalyst_interaction_via_a_short_cyanide_bridge_for_water_oxidation.pdf: 3932767 bytes, checksum: 8d8e05feedb86e5432ab8017a4713987 (MD5) Previous issue date: 2021-02-24 | en |
dc.identifier.doi | 10.1016/j.xcrp.2020.100319 | en_US |
dc.identifier.issn | 2666-3864 | |
dc.identifier.uri | http://hdl.handle.net/11693/77457 | |
dc.language.iso | English | en_US |
dc.publisher | Cell Press | en_US |
dc.relation.isversionof | https://doi.org/10.1016/j.xcrp.2020.100319 | en_US |
dc.source.title | Cell Reports Physical Science | en_US |
dc.subject | Photosensitizer-catalyst | en_US |
dc.subject | Dye-sensitized water splitting | en_US |
dc.subject | Cyanide chemistry | en_US |
dc.subject | Ruthenium-free | en_US |
dc.subject | Water oxidation | en_US |
dc.subject | Prussian blue | en_US |
dc.subject | Organic chromophore | en_US |
dc.subject | WO3 | en_US |
dc.subject | Photoelectrochemical | en_US |
dc.subject | Visible-light-absorbing semiconductors | en_US |
dc.title | Pushing the limits in photosensitizer-catalyst interaction via a short cyanide bridge for water oxidation | en_US |
dc.type | Article | en_US |
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