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Domain Purity, Miscibility, and Molecular Orientation at Donor/Acceptor Interfaces in High Performance Organic Solar Cells: Paths to Further Improvement

Domain Purity, Miscibility, and Molecular Orientation at Donor/Acceptor Interfaces in High... Domain purity and interface structure are known to be critical for fullerene‐based bulk heterojunction (BHJ) solar cells, yet have been very difficult to study. Using novel soft X‐ray tools, we delineate the importance of these parameters by comparing high performance cells based on a novel naphtha(1,2‐c:5,6‐c)bis(1,2,5)thiadiazole (NT) material to cells based on a 2,1,3‐benzothiadiazole (BT) analogue. BT‐based devices exhibit ∼15 nm, mixed domains that differ in composition by at most 22%, causing substantial bimolecular recombination. In contrast, NT‐based devices have more pure domains that are >80 nm in size, yet the polymer‐rich phase still contains at least 22% fullerene. Power conversion efficiency >6% is achieved for NT devices despite a domain size much larger than the nominal exciton diffusion length due to a favourable trade‐off in the mixed domain between exciton harvesting, charge transport, and bimolecular recombination. The miscibility of the fullerene with the NT and BT polymer is measured and correlated to the purity in devices. Importantly, polarized x‐ray scattering reveals preferential face‐on orientation of the NT polymer relative to the PCBM‐rich domains. Such ordering has previously not been observed in fullerene‐based solar cells and is shown here to be possibly a controlling or contributing factor to high performance. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Advanced Energy Materials Wiley

Domain Purity, Miscibility, and Molecular Orientation at Donor/Acceptor Interfaces in High Performance Organic Solar Cells: Paths to Further Improvement

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Publisher
Wiley
Copyright
Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
ISSN
1614-6832
eISSN
1614-6840
DOI
10.1002/aenm.201200912
Publisher site
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Abstract

Domain purity and interface structure are known to be critical for fullerene‐based bulk heterojunction (BHJ) solar cells, yet have been very difficult to study. Using novel soft X‐ray tools, we delineate the importance of these parameters by comparing high performance cells based on a novel naphtha(1,2‐c:5,6‐c)bis(1,2,5)thiadiazole (NT) material to cells based on a 2,1,3‐benzothiadiazole (BT) analogue. BT‐based devices exhibit ∼15 nm, mixed domains that differ in composition by at most 22%, causing substantial bimolecular recombination. In contrast, NT‐based devices have more pure domains that are >80 nm in size, yet the polymer‐rich phase still contains at least 22% fullerene. Power conversion efficiency >6% is achieved for NT devices despite a domain size much larger than the nominal exciton diffusion length due to a favourable trade‐off in the mixed domain between exciton harvesting, charge transport, and bimolecular recombination. The miscibility of the fullerene with the NT and BT polymer is measured and correlated to the purity in devices. Importantly, polarized x‐ray scattering reveals preferential face‐on orientation of the NT polymer relative to the PCBM‐rich domains. Such ordering has previously not been observed in fullerene‐based solar cells and is shown here to be possibly a controlling or contributing factor to high performance.

Journal

Advanced Energy Materials – Wiley

Published: Jul 1, 2013

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