| Literature DB >> 26263331 |
Jiewei Liu1, Sandeep Pathak1, Thomas Stergiopoulos1, Tomas Leijtens1, Konrad Wojciechowski1, Stefan Schumann, Nina Kausch-Busies, Henry J Snaith1.
Abstract
Organic-inorganic halide perovskite solar cells have recently emerged as high-performance photovoltaic devices with low cost, promising for affordable large-scale energy production, with laboratory cells already exceeding 20% power conversion efficiency (PCE). To date, a relatively expensive organic hole-conducting molecule with low conductivity, namely spiro-OMeTAD (2,2',7,7'-tetrakis(N,N-di-p-methoxyphenyl-amine) 9,9'- spirobifluorene), is employed widely to achieve highly efficient perovskite solar cells. Here, we report that by replacing spiro-OMeTAD with much cheaper and highly conductive poly(3,4-ethylenedioxythiophene) (PEDOT) we can achieve PCE of up to 14.5%, with PEDOT cast from a toluene based ink. However, the stabilized power output of the PEDOT-based devices is only 6.6%, in comparison to 9.4% for the spiro-OMeTAD-based cells. We deduce that accelerated recombination is the cause for this lower stabilized power output and postulate that reduced levels of p-doping are required to match the stabilized performance of Spiro-OMeTAD. The entirely of the materials employed in the perovskite solar cell are now available at commodity scale and extremely inexpensive.Entities:
Keywords: PEDOT; hole transporting material; organometallic halide photovoltaic; perovskite; perovskite solar cells; photovoltaic; solar cells; spiro-OMeTAD
Year: 2015 PMID: 26263331 DOI: 10.1021/acs.jpclett.5b00545
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475