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dc.contributor.author Du, Zhonglin -
dc.contributor.author Pan, Zhenxiao -
dc.contributor.author Fabregat-Santiago, Francisco -
dc.contributor.author Zhao, Ke -
dc.contributor.author Long, Donghui -
dc.contributor.author Zhang, Hua -
dc.contributor.author Zhao, Yixin -
dc.contributor.author Zhong, Xinhua -
dc.contributor.author Yu, Jong-Sung -
dc.contributor.author Bisquert, Juan -
dc.date.available 2017-07-05T08:34:43Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016-08 -
dc.identifier.issn 1948-7185 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2210 -
dc.description.abstract The mean power conversion efficiency (PCE) of quantum-dot-sensitized solar cells (QDSCs) is mainly limited by the low photovoltage and fill factor (FF), which are derived from the high redox potential of polysulfide electrolyte and the poor catalytic activity of the counter electrode (CE), respectively. Herein, we report that this problem is overcome by adopting Ti mesh supported mesoporous carbon (MC/Ti) CE. The confined area in Ti mesh substrate not only offers robust carbon film with submillimeter thickness to ensure high catalytic capacity, but also provides an efficient three-dimension electrical tunnel with better conductivity than state-of-art Cu2S/FTO CE. More importantly, the MC/Ti CE can down shift the redox potential of polysulfide electrolyte to promote high photovoltage. In all, MC/Ti CEs boost PCE of CdSe0.65Te0.35 QDSCs to a certified record of 11.16% (Jsc = 20.68 mA/cm2, Voc = 0.798 V, FF = 0.677), an improvement of 24% related to previous record. This work thus paves a way for further improvement of performance of QDSCs. © 2016 American Chemical Society. -
dc.language English -
dc.publisher American Chemical Society -
dc.title Carbon Counter-Electrode-Based Quantum-Dot-Sensitized Solar Cells with Certified Efficiency Exceeding 11% -
dc.type Article -
dc.identifier.doi 10.1021/acs.jpclett.6b01356 -
dc.identifier.scopusid 2-s2.0-84983334880 -
dc.identifier.bibliographicCitation Journal of Physical Chemistry Letters, v.7, no.16, pp.3103 - 3111 -
dc.subject.keywordPlus Carbon Counter Electrodes -
dc.subject.keywordPlus Carbon Films -
dc.subject.keywordPlus Catalyst Activity -
dc.subject.keywordPlus Confined Areas -
dc.subject.keywordPlus CONVERSION -
dc.subject.keywordPlus COPPER -
dc.subject.keywordPlus Counter Electrodes -
dc.subject.keywordPlus Dye -
dc.subject.keywordPlus Efficiency -
dc.subject.keywordPlus Electrodes -
dc.subject.keywordPlus Electrolytes -
dc.subject.keywordPlus ELECTROPHORETIC DEPOSITION -
dc.subject.keywordPlus Mesh Generation -
dc.subject.keywordPlus MESOPOROUS CARBON -
dc.subject.keywordPlus NANOCRYSTALS -
dc.subject.keywordPlus NANOPARTICULATE -
dc.subject.keywordPlus Nanotube -
dc.subject.keywordPlus PERFORMANCE -
dc.subject.keywordPlus PHOTOVOLTAICS -
dc.subject.keywordPlus Polyelectrolytes -
dc.subject.keywordPlus POLYSULFIDE ELECTROLYTE -
dc.subject.keywordPlus Polysulfides -
dc.subject.keywordPlus Quantum Dot-Sensitized Solar Cells -
dc.subject.keywordPlus RECOMBINATION -
dc.subject.keywordPlus Redox Potentials -
dc.subject.keywordPlus Redox Reactions -
dc.subject.keywordPlus Semiconductor Quantum Dots -
dc.subject.keywordPlus Solar Cells -
dc.subject.keywordPlus STABILITY -
dc.subject.keywordPlus Submillimeters -
dc.subject.keywordPlus Three Dimensions -
dc.citation.endPage 3111 -
dc.citation.number 16 -
dc.citation.startPage 3103 -
dc.citation.title Journal of Physical Chemistry Letters -
dc.citation.volume 7 -
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Department of Energy Science and Engineering Light, Salts and Water Research Group 1. Journal Articles

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