Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/141585
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dc.contributor.authorGurudayalen_US
dc.contributor.authorBeeman, Jeffrey W.en_US
dc.contributor.authorBullock, Jamesen_US
dc.contributor.authorWang, Haoen_US
dc.contributor.authorEichhorn, Johannaen_US
dc.contributor.authorTowle, Clarissaen_US
dc.contributor.authorJavey, Alien_US
dc.contributor.authorToma, Francesca M.en_US
dc.contributor.authorMathews, Nripanen_US
dc.contributor.authorAger, Joel W.en_US
dc.date.accessioned2020-06-09T06:14:44Z-
dc.date.available2020-06-09T06:14:44Z-
dc.date.issued2019-
dc.identifier.citationGurudayal, Beeman, J. W., Bullock, J., Wang, H., Eichhorn, J., Towle, C., . . . Ager, J. W. (2019). Si photocathode with Ag-supported dendritic Cu catalyst for CO2 reduction. Energy & Environmental Science, 12(3), 1068-1077. doi:10.1039/c8ee03547den_US
dc.identifier.issn1754-5692en_US
dc.identifier.urihttps://hdl.handle.net/10356/141585-
dc.description.abstractSi photocathodes integrated with Ag-supported dendritic Cu catalysts are used to perform light-driven reduction of CO2 to C2 and C3 products in aqueous solution. A back illumination geometry with an n-type Si absorber was used to permit the use of absorbing metallic catalysts. Selective carrier collection was accomplished by a p+ implantation on the illumination side and an n+ implantation followed by atomic layer deposition of TiO2 on the electrolyte site. The Ag-supported dendritic Cu CO2 reduction catalyst was formed by evaporation of Ag followed by high-rate electrodeposition of Cu to form a high surface area structure. Under simulated 1 sun illumination in 0.1 M CsHCO3 saturated with CO2, the photovoltage generated by the Si (∼600 mV) enables C2 and C3 products to be produced at −0.4 vs. RHE. Texturing of both sides of the Si increases the light-limited current density, due to reduced reflection on the illumination side, and also deceases the onset potential. Under simulated diurnal illumination conditions photocathodes maintain over 60% faradaic efficiency to hydrocarbon and oxygenate products (mainly ethylene, ethanol, propanol) for several days. After 10 days of testing, contamination from the counter electrode is observed, which causes an increase in hydrogen production. This effect is mitigated by a regeneration procedure which restores the original catalyst selectivity. A tandem, self-powered CO2 reduction device was formed by coupling a Si photocathode with two series-connected semitransparent CH3NH3PbI3 perovskite solar cells, achieving an efficiency for the conversion of sunlight to hydrocarbons and oxygenates of 1.5% (3.5% for all products).en_US
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.language.isoenen_US
dc.relation.ispartofEnergy & Environmental Scienceen_US
dc.rights© 2019 The Royal Society of Chemistry. All rights reserved. This paper was published in Energy & Environmental Science and is made available with permission of The Royal Society of Chemistry.en_US
dc.subjectEngineering::Materialsen_US
dc.titleSi photocathode with Ag-supported dendritic Cu catalyst for CO2 reductionen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Materials Science and Engineeringen_US
dc.contributor.researchEnergy Research Institute @ NTU (ERI@N)en_US
dc.contributor.researchResearch Techno Plazaen_US
dc.identifier.doi10.1039/c8ee03547d-
dc.description.versionAccepted versionen_US
dc.identifier.issue3en_US
dc.identifier.volume12en_US
dc.identifier.spage1068en_US
dc.identifier.epage1077en_US
dc.subject.keywordsPhotocathodeen_US
dc.subject.keywordsCO2 Reductionen_US
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