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Royal Society of Chemistry, Energy & Environmental Science, 1(7), p. 399-407, 2014

DOI: 10.1039/c3ee43161d

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The origin of high efficiency in low-temperature solution-processable bilayer organometal halide hybrid solar cells

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This paper is available in a repository.

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Abstract

This work reports a study into the origin of the high efficiency in solution-processable bilayer solar cells based on methylammonium lead iodide (CH 3 NH 3 PbI 3) and [6,6]-phenyl-C 61 -butyric acid methyl ester (PC 61 BM). Our cell has a power conversion efficiency (PCE) of 5.2% under simulated AM 1.5G irradiation (100 mW cm À2) and an internal quantum efficiency of close to 100%, which means that nearly all the absorbed photons are converted to electrons and are efficiently collected at the electrodes. This implies that the exciton diffusion, charge transfer and charge collection are highly efficient. The high exciton diffusion efficiency is enabled by the long diffusion length of CH 3 NH 3 PbI 3 relative to its thickness. Furthermore, the low exciton binding energy of CH 3 NH 3 PbI 3 implies that exciton splitting at the CH 3 NH 3 PbI 3 /PC 61 BM interface is very efficient. With further increase in CH 3 NH 3 PbI 3 thickness, a higher PCE of 7.4% could be obtained. This is the highest efficiency attained for low temperature solution-processable bilayer solar cells to date.