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Issue 14, 2018
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Hole transporting materials based on benzodithiophene and dithienopyrrole cores for efficient perovskite solar cells

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Abstract

The development of highly efficient hole transporting materials (HTMs) for perovskite solar cells (PSCs) is still one of the most thrilling research subjects in the development of this emerging photovoltaic technology. Inner ring engineering of the aromatic core of new HTMs – consisting of three fused rings endowed with four triarylamine units – reveals major performance effects over the fabricated devices. In particular, substitution of the central pyrrole ring in dithienopyrrole (DTP) by a benzene ring – benzodithiophene (BDT) – allows enhancing the power conversion efficiency from 15.6% to 18.1%, in devices employing mixed-perovskite (FAPbI3)0.85(MAPbBr3)0.15 (MA: CH3NH3+, FA: NH[double bond, length as m-dash]CHNH3+) under 1 sun illumination. In comparison, 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (spiro-OMeTAD) yielded a power conversion efficiency of 17.7%. The novel HTM molecules show an efficient quenching of the perovskite photoluminescence, indicating an efficient charge transfer from the active layer to the HTM, along with a good conductivity (comparable to that of the spiro-OMeTAD reference). Density functional theory (DFT) calculations allowed rationalizing the electrochemical and optical properties and predicting a reorganization energy (λ) for the best performing BDT-based HTM (0.101 eV) significantly lower than that computed for the benchmark spiro-OMeTAD (0.139 eV).

Graphical abstract: Hole transporting materials based on benzodithiophene and dithienopyrrole cores for efficient perovskite solar cells

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Publication details

The article was received on 27 Dec 2017, accepted on 23 Feb 2018 and first published on 26 Feb 2018


Article type: Paper
DOI: 10.1039/C7TA11314E
Citation: J. Mater. Chem. A, 2018,6, 5944-5951
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    Hole transporting materials based on benzodithiophene and dithienopyrrole cores for efficient perovskite solar cells

    R. Sandoval-Torrientes, I. Zimmermann, J. Calbo, J. Aragó, J. Santos, E. Ortí, N. Martín and M. K. Nazeeruddin, J. Mater. Chem. A, 2018, 6, 5944
    DOI: 10.1039/C7TA11314E

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