• Andritsch, Thomas
• Fabiani, Davide
• Rosa, Marcello La
• Li, Chuanyang
• Lei, Zhipeng
• Bray, Tommaso
• Credi, Alberto
• Wang, Xinyu

Abstract

This paper deals with the role played by the interface and bulk volume of the nanofiller about affecting the electrical properties of a nanocomposite material. For this purpose, a simple and completely amorphous matrix, polystyrene (PS), is used as base material, and core-shell quantum dots are exploited for simulating the structure of nanocomposites: CdSe core and CdSe-ZnS core-shell semiconductor quantum dots (QDs) are added into a PS matrix. The latter is to highlight the effect of the ZnS interface and as contrast to the core material. Dispersion and distribution of QDs are first microscopically observed and optimized, by including isopropyl alcohol in the manufacturing phase as an additional solvent. Among electrical properties the focus is on space charge accumulation, tested by means of the pulsed electroacoustic technique at 10 kV/mm and 50 kV/mm on CdSe and CdSe-ZnS doped PS composites. Results are then compared with a reference PS without QDs. Trap depth and density are also obtained by space charge measurement results. When CdSe QDs are added to PS, the trap density increases with respect to the baseline values measured on the unfilled polymer. In contrast, the ZnS shell around the CdSe core creates an additional trap level with lower trap depth, which increases charge mobility, thus turning homocharge into heterocharge accumulation. Therefore, the surface shell-structure of QD nanocrystals appears to significantly influence the space charge behavior of the nanocomposite, independently of the polymer.

Topics

• nanocomposite
• density
• impedance spectroscopy
• dispersion
• surface
• polymer
• amorphous
• phase
• mobility
• semiconductor
• alcohol
• quantum dot