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Hole transporting materials based on benzodithiophene and dithienopyrrole cores for efficient perovskite solar cells
Ist Teil von
Journal of materials chemistry. A, Materials for energy and sustainability, 2018-01, Vol.6 (14), p.5944-5951
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2018
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
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 (FAPbI
3
)
0.85
(MAPbBr
3
)
0.15
(MA: CH
3
NH
3
+
, FA: NH&z.dbd;CHNH
3
+
) 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).
High efficiency (18.1%) perovskite solar cells are demonstrated by using a hole transporting material with very low reorganization energy (
λ
).