Open-Circuit Voltage Losses in Selenium-Substituted Organic Photovoltaic Devices from Increased Density of Charge-Transfer States
Open-Circuit Voltage Losses in Selenium-Substituted Organic Photovoltaic Devices from Increased Density of Charge-Transfer States
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DOI:
10.1021/acs.chemmater.5b02133
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发表时间:
2015-09
影响因子:
8.6
通讯作者:
Dana B. Sulas;Kai Yao;Jeremy J. Intemann;Spencer T. Williams;Chang‐Zhi Li;Chu‐Chen Chueh;J. J. Richards-J.;Yuyin Xi;L. Pozzo;Cody W. Schlenker;A. Jen;D. Ginger
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作者:
Dana B. Sulas;Kai Yao;Jeremy J. Intemann;Spencer T. Williams;Chang‐Zhi Li;Chu‐Chen Chueh;J. J. Richards-J.;Yuyin Xi;L. Pozzo;Cody W. Schlenker;A. Jen;D. Ginger
Using an analysis based on Marcus theory, we characterize losses in open-circuit voltage (VOC) due to changes in charge-transfer state energy, electronic coupling, and spatial density of charge-transfer states in a series of polymer/fullerene solar cells. We use a series of indacenodithiophene polymers and their selenium-substituted analogs as electron donor materials and fullerenes as the acceptors. By combining device measurements and spectroscopic studies (including subgap photocurrent, electroluminescence, and, importantly, time-resolved photoluminescence of the charge-transfer state) we are able to isolate the values for electronic coupling and the density of charge-transfer states (NCT), rather than the more commonly measured product of these values. We find values for NCT that are surprisingly large (∼4.5 × 1021–6.2 × 1022 cm–3), and we find that a significant increase in NCT upon selenium substitution in donor polymers correlates with lower VOC for bulk heterojunction photovoltaic devices. The inc...