Abstract
Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is less selective for holes in an inverted-architecture organic photovoltaic (OPV) than it is in a conventional-architecture OPV device due to differences between the interfacial-PSS concentration at the top and bottom of the PEDOT:PSS layer. In this work, thin layers of polysulfonic acids are inserted between the poly(3-hexylthiophene) (P3HT):indene-C60 bisadduct (ICBA) bulk heterojunction (BHJ) active layer and PEDOT:PSS to create a higher concentration of acid at this interface and, therefore, mimic the distribution of materials present in a conventional device. Upon thermal annealing, this acid layer oxidizes P3HT, creating a thin p-type interlayer of P3HT+/acid- on top of the BHJ. Using X-ray absorption spectroscopy, Kelvin probe, and ellipsometry measurements, this P3HT+/acid- layer is shown to be insoluble in water, indicating it remains intact during the subsequent deposition of PEDOT:PSS. Current density-voltage measurements show this doped interlayer reduces injected dark current while increasing both open-circuit voltage and fill factor through the creation of a more hole selective BHJ-PEDOT:PSS interface.
Original language | American English |
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Article number | 1500346 |
Journal | Advanced Materials Interfaces |
Volume | 3 |
Issue number | 2 |
DOIs | |
State | Published - 2016 |
Bibliographical note
Publisher Copyright:© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
NREL Publication Number
- NREL/JA-5900-64540
Keywords
- charge selectivity
- doping
- interlayers
- organic photovoltaics