期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 119, 期 23, 页码 12792-12800出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp512627e
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资金
- Catalysis for Sustainable Energy (CASE) initiative - Catalysis for Sustainable Energy (CASE) initiative
- Danish Council for Independent Research's DFF-Sapere Aude program [11-1051390]
The shift from iodide-based redox mediators in dye-sensitized solar cells toward octahedral cobalt complexes has led to a significant increase in the efficiency. However, due to the nature of this type of complexes the driving force required for the regeneration of the dye is very high, and this limits the achievable efficiency. Here we show that the large driving force is a direct consequence of the large reorganization energy of the dye regeneration reaction. The reorganization energies for charge transfer between a simple zinc porphyrin dye and two popular cobalt-based redox mediators is calculated using ab initio molecular dynamics with explicit solvent. These results are then combined with a Marcus-based extrapolation scheme to obtain the reorganization energies of more than 5000 porphyrin-based dyes. We propose a scheme for scoring the performance of the porphyrin dyes, which is able to identify already known high-performance dyes in addition to a number of even better candidates. Our analysis shows that the large internal reorganization energy of the Co-based redox mediators is an obstacle for achieving higher efficiencies.
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