A New Mussel-Inspired Polydopamine Sensitizer for Dye-Sensitized Solar Cells: Controlled Synthesis and Charge Transfer
- Authors
- Nam, Hye Jin; Kim, Boeun; Ko, Min Jae; Jin, Mingshi; Kim, Ji Man; Jung, Duk-Young
- Issue Date
- 2012-10
- Publisher
- WILEY-V C H VERLAG GMBH
- Citation
- CHEMISTRY-A EUROPEAN JOURNAL, v.18, no.44, pp.14000 - 14007
- Abstract
- The efficient electron injection by direct dye-to-TiO2 charge transfer and strong adhesion of mussel-inspired synthetic polydopamine (PDA) dyes with TiO2 electrode is demonstrated. Spontaneous self-polymerization of dopamine using dip-coating (DC) and cyclic voltammetry (CV) in basic buffer solution were applied to TiO2 layers under a nitrogen atmosphere, which offers a facile and reliable synthetic pathway to make the PDA dyes, PDA-DC and PDA-CV, with conformal surface and perform an efficient dye-to-TiO2 charge transfer. Both synthetic methods led to excellent photovoltaic results and the PDA-DC dye exhibited larger current density and efficiency values than those in the PDA-CV dye. Under simulated AM 1.5 G solar light (100 mW cm(-2)), a PDA-DC dye exhibited a short circuit current density of 5.50 mW cm(-2), corresponding to an overall power conversion efficiency of 1.2%, which is almost 10 times that of the dopamine dye-sensitized solar cell. The PDA dyes showed strong adhesion with the nanocrystalline TiO2 electrodes and the interface engineering of a dye-adsorbed TiO2 surface through the control of the coating methods, reaction times and solution concentration maximized the overall conversion efficiency, resulting in a remarkably high efficiency.
- Keywords
- OPTICAL-PROPERTIES; TIO2; EFFICIENCY; MELANIN; NANOPARTICLES; ROUTE; LIGHT; CONVERSION; LIGAND; GROWTH; OPTICAL-PROPERTIES; TIO2; EFFICIENCY; MELANIN; NANOPARTICLES; ROUTE; LIGHT; CONVERSION; LIGAND; GROWTH; charge transfer; dopamines; polymerization; sensitizers; solar cells
- ISSN
- 0947-6539
- URI
- https://pubs.kist.re.kr/handle/201004/128821
- DOI
- 10.1002/chem.201202283
- Appears in Collections:
- KIST Article > 2012
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