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dc.contributor.author Kim, Seonghun -
dc.contributor.author Park, Yiseul -
dc.contributor.author Kim, Wooyul -
dc.contributor.author Park, Hyunwoong -
dc.date.available 2017-07-11T05:41:39Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016 -
dc.identifier.issn 1474-905X -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2786 -
dc.description.abstract CdS and WO3 (CdS/WO3) bilayer film electrodes are fabricated to harness solar visible light (λ > 420 nm) and store photogenerated electrons for possible use during periods of unavailable sunlight. The overall film thickness is approximately 50-60 μm, while the CdS underlayer is slightly thinner than WO3 owing to a packing effect. The energetics of CdS and WO3 determined by optical and electrochemical analyses enables cascaded electron transfer from CdS to WO3. The open circuit potential (EOCP) of CdS/WO3 under visible light (approximately -0.35 V vs. SCE) is nearly maintained even in the absence of light, with a marginal decrease (∼0.15 V) in ∼20 h of darkness. Neither CdS nor WO3 alone exhibits such behavior. The electron lifetimes (τ) of CdS and WO3 are each less than 100 s, whereas coupling of the two increases τ to ∼2500 s at the EOCP. In the absence of dissolved O2, τ further increases, suggesting that O2 is the primary electron acceptor. In spite of oxic conditions, CdS/WO3 is capable of continuously reducing Cr6+ to Cr3+ and Ag+ to Ag0 after removal of visible light. The number of utilized (i.e., stored) electrons in the reductions of Cr6+ and Ag+ are estimated to be ∼1.08 × 1017 and ∼0.87 × 1017, respectively. The primary role of CdS is to be a visible-light absorber in the 420-565 nm wavelength range, transferring the photogenerated electrons to WO3. The electrons stored in WO3 are gradually released to electron acceptors with suitable redox potentials. © The Royal Society of Chemistry and Owner Societies 2016. -
dc.publisher Royal Society of Chemistry -
dc.title Harnessing and storing visible light using a heterojunction of WO3 and CdS for sunlight-free catalysis -
dc.type Article -
dc.identifier.doi 10.1039/c6pp00091f -
dc.identifier.scopusid 2-s2.0-84982747255 -
dc.identifier.bibliographicCitation Photochemical and Photobiological Sciences, v.15, no.8, pp.1006 - 1011 -
dc.subject.keywordPlus BiVO4 -
dc.subject.keywordPlus CO2 -
dc.subject.keywordPlus COPPER -
dc.subject.keywordPlus ENERGY-STORAGE -
dc.subject.keywordPlus NANOPARTICLES -
dc.subject.keywordPlus Photosynthesis -
dc.subject.keywordPlus SYSTemS -
dc.subject.keywordPlus WATER -
dc.citation.endPage 1011 -
dc.citation.number 8 -
dc.citation.startPage 1006 -
dc.citation.title Photochemical and Photobiological Sciences -
dc.citation.volume 15 -
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