Related Experiment Video
Updated: Aug 13, 2026

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Inclusion of Piperidine Side-Chain in Cathode Interlayer Materials Toward Improved Stability in Organic Solar Cells
Jiashuai Wang1, Ting Wang1, Wei Xiong1
1Institute of Polymer Optoelectronic Materials and Devices, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou, P. R. China.
Abstract:
Lab-scale Organic solar cells (OSCs) have achieved remarkable progress with state-of-the-art power conversion efficiencies (PCE) exceeding 20%. However, they are still confronted with inadequate device lifetime resulting from instabilities in either material structures or film morphologies of the active layer and interfacial layers. Here, we designed and synthesized a cathode interlayer (CIL) material, NDI-N-P. By replacing the commonly used linear amine side-chain with a cyclic amine, piperidine. The negative effects of the linear amine side-chain on the acceptor in the active layer are largely mitigated via the improved steric hindrance of piperidine. OSC devices based on NDI-N-P achieve a PCE of 19.8% and demonstrate improved long-term stability, showcasing the potential of tailoring the local structure of CILs toward highly efficient and stable OSCs. Furthermore, we tailored the aryl terminal groups to obtain an extra CIL molecule, NDI-I-P, with isoquinolyl side-groups to investigate the influence of electron-withdrawing ability of terminal groups on the self-doping effects within the molecules and the performance of resulting devices. This provides insights for further regulating the photoelectric and aggregate properties of CILs toward enhanced electron extraction in OSCs.
More Related Videos
06:49In situ Grazing Incidence Small Angle X-ray Scattering on Roll-To-Roll Coating of Organic Solar Cells with Laboratory X-ray Instrumentation
Published on: March 2, 2021
08:29Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Related Concept Videos
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
Pericyclic Reactions: Introduction
Pericyclic reactions can be classified into three categories: electrocyclic reactions, cycloaddition reactions, and sigmatropic rearrangements. Electrocyclic reactions and sigmatropic rearrangements are...
Radical Reactivity: Steric Effects
Along with electronic factors, steric factors also account...
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
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.