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Influence of Environmentally Affected Hole Transport Layers on Spatial Homogeneity and Charge Transport Dynamics of Organic Solar Cells (1908.00135v1)

Published 24 Jun 2019 in physics.app-ph and cond-mat.mtrl-sci

Abstract: After the efficiency of organic photovoltaic (OPV) cells achieved more than 10%, the control of stability and degradation mechanisms of solar cells became a prominent task. The improvement of device efficiency due to incorporation of a hole-transport layer (HTL) in bulk-heterojunction solar cells has been extensively reported. However, the most widely used HTL material, PEDOT:PSS is frequently suspected to be the dominating source for devices instability under environmental conditions. Thereby effects like photooxidation and electrode corrosion are often reported to shorten device lifetime. However, often in environmental device studies, the source of degradation, whether being from the HTL, the active layer or the metal cathode are rather difficult to distinguish, because the external diffusion of oxygen and water affects all components. In this study, different HTLs, namely prepared from traditional PEDOT:PSS and also two types of molybdenum trioxide (MoO3), are exposed to different environments such as oxygen, light or humidity, prior to device finalization under inert conditions. This allows investigating any effects within the HTL and from reactions at its interface to the indium-tin-oxide electrode or the active layer. The surface and bulk chemistry of the exposed HTL has been monitored and discussed in context to the observed device physics, dynamic charge transport and spatial performance homogeneity of the according OPV device. The results show that merely humidity-exposure of the HTL leads to decreased device performance for PEDOT:PSS, but also for one type of the tested MoO3. The losses are related to the amount of absorbed water in the HTL, inducing loss of active area in terms of interfacial contact. The device with PEDOT:PSS HTL after humid air exposure showed seriously decreased photocurrent by micro-delamination of swelling/shrinkage of the hygroscopic layer.

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