TY - JOUR
T1 - Contact doping with sub-monolayers of strong polyelectrolytes for organic photovoltaics
AU - Mor, Gopal K.
AU - Jones, David
AU - Le, Thinh P.
AU - Shang, Zhengrong
AU - Weathers, Patrick J.
AU - Woltermann, Megumi K.B.
AU - Vakhshouri, Kiarash
AU - Williams, Bryan P.
AU - Tohran, Sarah A.
AU - Saito, Tomonori
AU - Verduzco, Rafael
AU - Salleo, Alberto
AU - Hickner, Michael A.
AU - Gomez, Enrique D.
N1 - Publisher Copyright:
© 2014 Wiley-VCH Verlag GmbH & Co. KGaA.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Barriers to charge transfer at electrode-semiconductor contacts are ubiquitous and limit the applicability of organic semiconductors in electronic devices. Molecular or ionic doping near contacts can alleviate charge injection or extraction problems by enabling charge tunneling through contact barriers, but the soft nature of organic materials allows for small molecule dopants to diffuse and migrate, degrading the performance of the device and limiting effective interfacial doping. Here, it is demonstrated that contact doping in organic electronics is possible through ionic polymer dopants, which resist diffusion or migration due to their large size. Sub-monolayer deposition of non-conjugated strong polyelectrolytes, e.g., sulfonated poly(sulfone)s, at the anode-semiconductor interface of organic photovoltaics enables effi cient hole extraction at the anode. The performance of contact-doped organic photovoltaics nearly matches the performance of devices composed of traditional hole transport layers such as poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS). The degree of sulfonation of the dopant polymer and the thickness of the ionic dopant layer is shown to be critical for optimizing doping and the effi ciency of the device.
AB - Barriers to charge transfer at electrode-semiconductor contacts are ubiquitous and limit the applicability of organic semiconductors in electronic devices. Molecular or ionic doping near contacts can alleviate charge injection or extraction problems by enabling charge tunneling through contact barriers, but the soft nature of organic materials allows for small molecule dopants to diffuse and migrate, degrading the performance of the device and limiting effective interfacial doping. Here, it is demonstrated that contact doping in organic electronics is possible through ionic polymer dopants, which resist diffusion or migration due to their large size. Sub-monolayer deposition of non-conjugated strong polyelectrolytes, e.g., sulfonated poly(sulfone)s, at the anode-semiconductor interface of organic photovoltaics enables effi cient hole extraction at the anode. The performance of contact-doped organic photovoltaics nearly matches the performance of devices composed of traditional hole transport layers such as poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS). The degree of sulfonation of the dopant polymer and the thickness of the ionic dopant layer is shown to be critical for optimizing doping and the effi ciency of the device.
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U2 - 10.1002/aenm.201400439
DO - 10.1002/aenm.201400439
M3 - Article
AN - SCOPUS:84908122775
SN - 1614-6832
VL - 4
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 13
M1 - 1400439
ER -