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Cobalt Electrolyte/Dye Interactions in Dye-Sensitized Solar Cells: A Combined Computational and Experimental Study
被引:197
作者:
Mosconi, Edoardo
[1
]
Yum, Jun-Ho
[2
]
Kessler, Florian
[2
]
Gomez Garcia, Carlos J.
[3
]
Zuccaccia, Cristiano
[4
]
Cinti, Antonio
[1
,4
]
Nazeeruddin, Mohammad K.
[2
]
Graetzel, Michael
[2
]
De Angelis, Filippo
[1
]
机构:
[1] Ist CNR Sci & Tecnol Mol, Computat Lab Hybrid & Organ Photovolta, I-06123 Perugia, Italy
[2] Swiss Fed Inst Technol, Lab Photon & Interfaces, Inst Chem Sci & Engn, Sch Basic Sci, CH-1015 Lausanne, Switzerland
[3] Univ Valencia, Inst Ciencia Mol Parque Cient, Paterna 46980, Valencia, Spain
[4] Univ Perugia, Dipartimento Chim, I-06123 Perugia, Italy
关键词:
DENSITY-FUNCTIONAL THEORY;
EFFECTIVE CORE POTENTIALS;
INTRAMOLECULAR ELECTRON-TRANSFER;
TRANSITION-METAL-COMPLEXES;
LOW QUANTUM YIELDS;
MOLECULAR CALCULATIONS;
REDOX ELECTROLYTE;
PHOTOVOLTAIC PERFORMANCE;
KEGGIN POLYOXOMETALATE;
POLYPYRIDYL COMPLEXES;
D O I:
10.1021/ja3079016
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We report a combined experimental and computational investigation to understand the nature of the interactions between cobalt redox mediators and TiO2 surfaces sensitized by :ruthenium and organic dyes, and their impact on. the performance of the corresponding dye-sensitized solar cells (DSSCs). We : focus: on different ruthenium dyes and fully organic dyes, to understand the dramatic loss of efficiency observed for the prototype Ru(II) N719 dye in conjunction with :Cobalt: electrolytes. Both N719- and Z907-based DSSCs showed an increased lifetime in iodine-based electrolyte compared to the cobalt-based redox-shuttle; While the organic D21L6 and D25L6 cycles endowed.With long alkoxy chains, show no significant:Change in the electron: lifetime regardless of employed electrolyte and deliver,a high photovoltaic efficiency of 6:5% with a cobalt electrolyte. Ab initio molecular dynamics simulations show the formation of.a complex between the cobalt electrolyte and the : surface-adsorbed ruthenium dye, which brings the [Co(bpy)(3)](3+) species' into Contact, with the TiO2 surface. This translates into a high probability of intercepting TiO2 injected electrons by the oxidized [Co(bpy)(3)](3+). species, lying close the N719-sensitized TiO2 surface. Investigation of the dye regeneration Mechanism by :the. cobalt electrolyte in the Marcus theory framework led, to substantially different reorganization energies for the high-spin (HS) and low:. spin (LS) reaction pathways. Our calculated reorganization energies. for the LS pathways are in excellent agreement with recent data for a series Of cobalt complexes, lending support to the proposed regeneration pathway. we systematically investigate. a series of Co(II)/Co(III) omplexes, to gauge the impact of ligand:substitution,and of metal coordination (tris-bidentate vs:.bis-tridentate) on the HS/LS.energy difference and reorganization energies. Our results allow us to trace structure/property. relations required for further development of cobalt electrolytes for DSSCs;
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页码:19438 / 19453
页数:16
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