Related Experiment Video
Updated: Jun 23, 2025

Influence of Hybrid Perovskite Fabrication Methods on Film Formation, Electronic Structure, and Solar Cell Performance
Published on: February 27, 2017
Improving the performance of perovskite solar cells by extending π-conjugation system
1Department of Inorganic Chemistry, Faculty of Chemistry, University of Mazandaran Babolsar Iran B.pashaei@umz.ac.ir.
Abstract:
In perovskite solar cells (PSCs), hole transporting materials (HTMs) play a critical role in determining the stability and efficiency of the devices. However, the high cost and complex synthesis processes associated with conventional HTMs can hinder their widespread applications. This work presents a low-cost and efficient HTM, namely N,N'-(naphthalene-1,5-diyl)bis(1-(dibenzo[a,c]phenazin-11-yl)-1-phenylmethanimine) (PEDN), based on a naphthalene core with an extended π-conjugation system for improving the performance of PSCs. The PEDN was synthesized via a facile two-step condensation method, eliminating the need for expensive catalysts such as BINAP. The newly developed HTM with an extended π-conjugation length was compared with BEDN and spiro-OMeTAD as the benchmark HTM, in terms of their optical, electrochemical, hole mobility properties, and efficiency in PSCs. The PEDN showed suitable highest occupied molecular orbital levels (HOMOs), good hole mobilities, as well as strong hydrophobicities. The extended π-conjugation system in PEDN contributes to the stability of the solar cells. The PSCs fabricated with PEDN achieved a high efficiency of 18.61%, comparable to the efficiency obtained using the commonly used HTM spiro-OMeTAD (19.68%). Furthermore, the cost-effectiveness of PEDN makes it a suitable alternative to spiro-OMeTAD for PSC applications.
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
P-N junction
UV–Vis Spectroscopy of Conjugated Systems
One of the factors influencing λmax is the extent...
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
UV–Vis Spectroscopy: Woodward–Fieser Rules

