Abstract

Organic photovoltaic systems comprising donor polymers and acceptor fullerene derivatives are attractive for inexpensive energy harvesting. Extensive research on polymer solar cells has provided insight into the factors governing device-level efficiency and stability. However, the detailed investigation of nanoscale structures is still challenging. Here we demonstrate the analysis and modification of unidentified surface aggregates. The aggregates are characterized electrically by Kelvin probe force microscopy and conductive atomic force microscopy (C-AFM), whereby the correlation between local electrical potential and current confirms a defective charge transport. Bimodal AFM modification confirms that the aggregates exist on top of the solar cell structure, and is used to remove them and to reveal the underlying active layer. The systematic analysis of the surface aggregates suggests that the structure consists of PCBM molecules.

Highlights

  • Polymer solar cells (PSCs) [1] have been widely studied due to the abundance of their constituents, their mechanical flexibility and light weight, as well as the possibility of low-cost roll-toroll mass production [2]

  • Due to the complicated nanoscale three-dimensional distribution of donor and acceptor materials in bulk heterojunction (BHJ) structures, atomic force microscopy (AFM) has been a very useful tool to observe the dependence of performance on the local morphology of PSCs [15], providing insights into the operating mechanism of PSCs

  • Among all the available modes of AFM, conductive AFM (C-AFM) and Kelvin probe force microscopy (KPFM) are the most widely used for PSC research, since the measured current and electrical potential can reveal local charge transport characteristics and the distribution of carriers and materials, which are relevant to device performance [16]

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Summary

Introduction

Polymer solar cells (PSCs) [1] have been widely studied due to the abundance of their constituents, their mechanical flexibility and light weight, as well as the possibility of low-cost roll-toroll mass production [2]. We performed KPFM measurements on both the DCB- and CB-cast samples to examine possible surface potential changes due to morphology differences of the PSC active layers.

Results
Conclusion
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