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;
引用
收藏
页码:19438 / 19453
页数:16
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