The evolution of surfaces and mechanisms of contact electrification between metals and polymers

Contact electrification (CE) is a pretty common phenomenon, but still is poorly understood. The long-standing controversy over the mechanisms of CE related to polymers is particularly intense due to their complexity. In this paper, the CE between metals and polymers is systematically studied, which shows the evolution of surfaces accompanied by variations of CE outputs. The variations of CE charge are closely related to the creep and deformation of the polymer and metal surfaces. Then the relationship between CE and polymer structures is put forward, which is essentially determined by the electronegativity of elements and the functional groups in the polymers. The effects of load and contact frequency on the CE process and outputs are also investigated, indicating the increase of CE charge with load and frequency. Material transfer from polymer to metal is observed during CE while electrons transfer from metal to polymer, both of which are believed to have an influence on each other. The findings advance our understanding on the mechanism of CE between metal and polymers, and provides insights into the performance of CE-based application in various conditions, which sheds light on the design and optimization of CE-based energy harvest and self-powered sensing devices.

Contact-electro-catalysis for the degradation of organic pollutants using pristine dielectric powders

Mechanochemistry has been studied for some time, but research on the reactivity of charges exchanged by contact-electrification (CE) during mechanical stimulation remains scarce. Here, we demonstrate that electrons transferred during the CE between pristine dielectric powders and water can be utilized to directly catalyze reactions without the use of conventional catalysts. Specifically, frequent CE at Fluorinated Ethylene Propylene (FEP) - water interface induces electron-exchanges, thus forming reactive oxygen species for the degradation of an aqueous methyl orange solution. Contact-electro-catalysis, by conjunction of CE, mechanochemistry and catalysis, has been proposed as a general mechanism, which has been demonstrated to be effective for various dielectric materials, such as Teflon, Nylon-6,6 and rubber. This original catalytic principle not only expands the range of catalytic materials, but also enables us to envisage catalytic processes through mechano-induced contact-electrification.

On chain models for contact electrification

An exact analytical model of charge dynamics for a chain of atoms with asymmetric hopping terms is presented. Analytic and numeric results are shown to give rise to similar dynamics in both the absence and presence of electron interactions. The chain model is further extended to the case of two atoms per cell (a perfect alloy system). This extension is further applied to contact electrification between two different atomic chains and the effect of increasing the magnitude of the contact transfer matrix element is studied.

Contact Electrification through Interfacial Charge Transfer: A Mechanistic Viewpoint on Solid-liquid interface

Contact Electrification (Triboelectrification) has been a long-standing phenomenon for 2600 years. The scientific understanding of contact electrification (triboelectrification) remains un-unified as the term itself implies complex phenomena involving mechanical contact/sliding...

Research on Controlling Contact Electrification by Modification of Cellulose Molecule Surface with Amino Group

As a green material, cellulose is widely used in friction triboelectric nanogenerators (TENGs). However, the weak polarity of the cellulose surface leads to its weak contact electrification performance, which is not conducive to its utilization in TENGs. In this study, epoxy chloropropane and ethylenediamine were grafted onto cellulose to form paper and were assembled with an FEP film. The output voltage, current, and surface charge density were 34.9%, 26.7%, and 16.7% higher than those of ordinary paper, respectively. When 20% nano TiO2 filler was added to the paper made from amino-modified cellulose, the output voltage, current, and surface charge density of the TENG increased by 70.9%, 226.7%, and 122.2%, respectively, compared with ordinary paper. As the air humidity of the TENG increased from 60% to 90%, the output voltage, current, and surface charge density were maintained at 53.7%, 38.9%, and 61.0%, respectively. When a 5 × 107 Ω resistor was connected to the working circuit, its output power reached 13.78 μ W·cm2. This showed that cellulose as a green material has wide application prospects in the field of TENG.