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Kim, Jin Young
Next Generation Energy Laboratory
Research Interests
  • Polymer solar cells, QD solar cells, organic-inorganic hybrid solar cells, perovskite solar cells, OLEDs, PeLEDs, organic FETs

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Spectroscopically tracking charge separation in polymer : fullerene blends with a three-phase morphology

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Title
Spectroscopically tracking charge separation in polymer : fullerene blends with a three-phase morphology
Author
Gallaher, Joseph K.Prasad, Shyamal K. K.Uddin, Mohammad A.Kim, TaehyoKim, Jin YoungWoo, Han YoungHodgkiss, Justin M.
Issue Date
2015-07
Publisher
ROYAL SOC CHEMISTRY
Citation
ENERGY & ENVIRONMENTAL SCIENCE, v.8, no.9, pp.2713 - 2724
Abstract
The coexistence of intermixed amorphous polymer : fullerene phases alongside pure semicrystalline polymer and fullerene phases provides a plausible explanation for effective charge separation in organic photovoltaic blends by providing a cascaded energy landscape. We sought to test this proposal by spectroscopically tracking charge dynamics in 3-phase blends compared with binary counterparts and linking these dynamics to free charge yields. Our study applies broadband transient absorption spectroscopy to a series of closely related alternating thiophene-benzothiadiazole copolymers in which the tuned curvature of the polymer backbone controls the nature and degree of polymer-fullerene intermixing. Free charge generation is most efficient in the 3-phase morphology that features intimately mixed polymer : PCBM regions amongst neat polymer and PCBM phases. TA spectral dynamics and polarization anisotropy measurements reveal the sub-nanosecond migration of holes from intermixed to pure polymer regions of such blends. In contrast, 2-phase blends lack the spectral dynamics of this charge migration process and suffer from severe geminate recombination losses. These results provide valuable spectroscopic evidence for an efficient charge separation pathway that relies on the 3-phase morphology
URI
https://scholarworks.unist.ac.kr/handle/201301/17121
URL
http://pubs.rsc.org/en/Content/ArticleLanding/2015/EE/C5EE01713K#!divAbstract
DOI
10.1039/c5ee01713k
ISSN
1754-5692
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