Related Experiment Video
Updated: Feb 7, 2026

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Donor-π-donor type hole transporting materials: marked π-bridge effects on optoelectronic properties, solid-state
S Paek1, I Zimmermann1, P Gao1
1Group for Molecular Engineering of Functional Materials , Ecole Polytechnique Federale de Lausanne Valais Wallis , Rue de l'Indutrie 17 , 1950 Sion , Valais , Switzerland . Email: mdkhaja.nazeeruddin@epfl.ch ;
Abstract:
Donor-π-bridge-donor type oligomers (D-π-D) have been studied intensively as active materials for organic optoelectronic devices. In this study, we introduce three new D-π-D type organic semiconductors incorporating thiophene or thienothiophene with two electron-rich TPA units, which can be easily synthesized from commercially available materials. A thorough comparison of their optoelectronic and structural properties was conducted, revealing the strong influence of the extent of longitudinal π-bridge conjugation on both the solid structure of the organic semiconductive materials and their photovoltaic performance when applied as hole transporting materials (HTM) in perovskite solar cells. Single-crystal measurements and time-resolved photoluminescence (TRPL) studies indicate that these coplanar donor-π-donor type HTMs could be promising alternatives to state-of-the-art spiro-OMeTAD, due to the multiple intermolecular short contacts as charge transporting channels and efficient charge extraction properties from the perovskite layer. The optimized devices with PEH-9 exhibited an impressive PCE of 16.9% under standard global AM 1.5 illumination with minimized hysteretic behaviour, which is comparable to that of devices using spiro-OMeTAD under similar conditions. Ambient stability after 400 h revealed that 93% of the energy conversion efficiency was retained for PEH-9, indicating that the devices had good long-term stability.
Related Concept Videos
π Electron Effects on Chemical Shift: Overview
Structures of Solids
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
π Molecular Orbitals of the Allyl Radical
The allyl systems have identical molecular orbitals but differ in the number of π electrons....
π Molecular Orbitals of the Allyl Cation and Anion

