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Post-Assembly Atomic Layer Deposition of Ultrathin Metal-Oxide Coatings Enhances the Performance of an Organic Dye-Sensitized Solar Cell by Suppressing Dye Aggregation
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Title
Post-Assembly Atomic Layer Deposition of Ultrathin Metal-Oxide Coatings Enhances the Performance of an Organic Dye-Sensitized Solar Cell by Suppressing Dye Aggregation
Issued Date
2015-03
Citation
Son, Ho-Jin. (2015-03). Post-Assembly Atomic Layer Deposition of Ultrathin Metal-Oxide Coatings Enhances the Performance of an Organic Dye-Sensitized Solar Cell by Suppressing Dye Aggregation. ACS Applied Materials & Interfaces, 7(9), 5150–5159. doi: 10.1021/am507405b
Type
Article
Author Keywords
dye-sensitized solar cells (DSCs)atomic layer deposition (ALD)dye aggregationpost-treatmentinterfacial electron injection
Keywords
INTERFACIAL ELECTRON-TRANSFERHIGHLY EFFICIENTLIGHT HARVESTERSTIO2STABILIZATIONCHROMOPHORESFLUORESCENCEDERIVATIVESRELAXATIONMOLECULES
ISSN
1944-8244
Abstract
Dye aggregation and concomitant reduction of dye excited-state lifetimes and electron-injection yields constitute a significant mechanism for diminution of light-to-electrical energy conversion efficiencies in many dye-sensitized solar cells (DSCs). For TiO2-based DSCs prepared with an archetypal donor-acceptor organic dye, (E)-2-cyano-3-(5′-(5′′-(p-(diphenylamino)phenyl)-thiophen-2′′-yl)thiophen-2′-yl)acrylic acid (OrgD), we find, in part via ultrafast spectroscopy measurements, that postdye-adsorption atomic layer deposition (ALD) of ultrathin layers of either TiO2 or Al2O3 effectively reverses residual aggregation. Notably, the ALD treatment is significantly more effective than the widely used aggregation-inhibiting coadsorbent, chenodeoxycholic acid. Primarily because of reversal of OrgD aggregation, and resulting improved injection yields, ALD post-treatment engenders a 30+% increase in overall energy conversion efficiency. A secondary contributor to increased currents and efficiencies is an ALD-induced attenuation of the rate of interception of injected electrons, resulting in slightly more efficient charge collection. © 2015 American Chemical Society.
URI
http://hdl.handle.net/20.500.11750/2921
DOI
10.1021/am507405b
Publisher
American Chemical Society
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