Characterization of Perovskite Solar Cells Using Frequency and Time Domain Techniques
Matthew Carnie a, Adam Pockett a b, Petra Cameron b
a SPECIFIC, Swansea University, Baglan Bay Innovation and Knowledge Centre, Baglan, SA12 7AX, United Kingdom
b Centre for Sustainable Chemical Technologies, University of Bath, Department of Chemistry, Claverton Down, Bath, BA27AY, United Kingdom
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV16)
Swansea, United Kingdom, 2016 June 29th - July 1st
Organizers: James Durrant, Henry Snaith and David Worsley
Poster, Adam Pockett, 279
Publication date: 28th March 2016

Despite a rapid rise in device record efficiencies, the level of understanding of the operation of perovskite solar cells is still some way behind. It is undoubtedly a promising material for the next-generation of commercially viable solar power generation, but for development to continue a number of issues need to be overcome. A better understanding of carrier transport and recombination processes will enable device architecture to be tuned for optimum performance. Also, an insight into the origins of the slow time response of these cells will help develop different material interfaces and reduce device hysteresis.

In this work, a range of complimentary characterisation techniques have been employed to study planar heterojunction devices. These techniques include electrochemical impedance spectroscopy, intensity modulated photovoltage/photocurrent spectroscopy and open-circuit photovoltage decay measurements. Of particular interest is the slow time/low frequency response when measured over a range of temperatures. These results show clear links to ionic diffusion within the devices, and provide good agreement with computational modelling. Evidence to support this includes the pronounced effect on open-circuit photovoltage decay rates even for a fairly modest range of temperatures. Activation energies calculated for this process agree well with calculated values for the diffusion of iodide ions through the perovskite layer. These results can be related to the origins of current-voltage hysteresis where a certain device state can be “locked-in” at low temperatures, at which ionic diffusion is restricted.



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