Modification of Electron Selective Contact in Perovskite Solar Cells by Self-assembled Monolayers of Fullerene Derivatives
Ivan Mora-Sero a, Emilio J. Juarez-Perez a, Marta Valles-Pelarda a, Victoria Gonzalez-Pedro a, Elena Mas-Marza a, Eva M. Barea a, Ileana B. Recalde a, Nazario Martín b, Agustin Molina b, Inés García-Benito b
a Universidad Complutense de Madrid/IMDEA-Nanociencia, Av. Séneca, 2, 28040 Madrid, Spain
Materials for Sustainable Development Conference (MATSUS)
Proceedings of nanoGe September Meeting 2015 (NFM15)
Santiago de Compostela, Spain, 2015 September 6th - 15th
Poster, Marta Valles-Pelarda, 255
Publication date: 8th June 2015

Hybrid Halide Perovskite are revolutionizing the photovoltaic field due to the high efficiencies obtained, as high as 20.1% of certified photoconversion efficiency, using solution processes at low temperature and consequently at low cost. However, the working principles of this kind of devices are not completely understood. Any photovoltaic devices needs a light absorbing material but also optimized selective contacts in order to produce an appropriated split of the Fermi levels. The work we present here focus on the modification of electron selective contact by the use of a self assembled monolayer of fullerene derivatives.

We have synthesized a series of fullerene derivatives containing a carboxylic acid functional group able to anchor to the TiO2 based electron selective contact. The carboxylic acid group works as head group by chemisorption onto the TiO2 surface allocating the fullerene moiety as tail functional group. The electron accepting properties of the fullerene derivatives have been characterized electrochemically and theoretically by Density Functional Theory. The effect of the fullerene derivative layer for the interfacial charge transfer or interfacial recombination processes has been analyzed and its implication on the solar cell performance is discussed in detail.



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