Related Experiment Video
Updated: Jan 1, 2026

Recombination Dynamics in Thin-film Photovoltaic Materials via Time-resolved Microwave Conductivity
Published on: March 6, 2017
Radiation-Induced Transient Currents in Films of Poly(arylene ether ketone) Including Phthalide Moiety
Evgenii D Pozhidaev1, Vera V Shaposhnikova2, Alexey R Tameev1,3
1National Research University Higher School of Economics, 101000 Moscow, Russia.
Abstract:
The electrical properties of thin films of poly(arylene ether ketone) copolymers (co-PAEKs) with a fraction of phthalide-containing units of 3, 5, and 50 mol% in the main chain were investigated by using radiation-induced conductivity (RIC) measurements. Transient current signals and current-voltage (I-V) characteristics were obtained by exposing 20 ÷ 25 μm thick films of the co-PAEKs to monoenergetic electron pulses with energy ranging from 3 to 50 keV in an electric field ranging from 5 to 40 V/μm. The Rose-Fowler-Vaisberg semi-empirical model based on a multiple trapping formalism was used for an analysis of the RIC data, and the parameters of the highly dispersive charge carrier transport were evaluated. The analysis revealed that charge carriers moved in isolation from each other, and the applied electric fields were below the threshold field triggering the switching effect (a reversible high-to-low resistivity transition) in the co-PAEK films. It was also found that the co-PAEK films, due to the super-linear I-V characteristics, are highly resistant to electrostatic discharges arising from the effects of ionizing radiation. This property is important for the development of protective coatings for electronic devices.
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Free-Radical Chain Reaction and Polymerization of Alkenes
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
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.
π Electron Effects on Chemical Shift: Overview
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds

