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.

The Magnetic Behaviour of CoTPP Supported on Coinage Metal Surfaces in the Presence of Small Molecules: A Molecular Cluster Study of the Surface trans-Effect

Density functional theory, combined with the molecular cluster model, has been used to investigate the surface trans-effect induced by the coordination of small molecules L (L = CO, NH3, NO, NO2 and O2) on the cobalt electronic structure of cobalt tetraphenylporphyrinato (CoTPP) surface-supported on coinage metal surfaces (Cu, Ag, and Au). Regardless of whether L has a closed- or an open-shell electronic structure, its coordination to Co takes out the direct interaction between Co and the substrate eventually present. The CO and NH3 bonding to CoTPP does not influence the Co local electronic structure, while the NO (NO2 and O2) coordination induces a Co reduction (oxidation), generating a 3d8 CoI (3d6 CoIII) magnetically silent closed-shell species. Theoretical outcomes herein reported demonstrate that simple and computationally inexpensive models can be used not only to rationalize but also to predict the effects of the Co–L bonding on the magnetic behaviour of CoTPP chemisorbed on coinage metals. The same model may be straightforwardly extended to other transition metals or coordinated molecules.

Assessment of Adhesion of Geopolymer and Varnished Coatings by the Pull-Off Method

This paper presents the results of testing the adhesion of geopolymer coatings and varnishes with ceramic additives to concrete and steel substrates. The measurement method used and described in this article was the pull-off method. The pull-off method test provides an easy way to evaluate the degree of adhesion of coatings to metal surfaces. The pull-off device provides values for the peel stress, which not only allows a quick determination of the adhesion of the coating to the substrate, but also makes it easier to compare the adhesion of several coatings to each other. However, this method requires appropriate preparation, so an attempt was made to determine its suitability for geopolymer layers. The results of testing the adhesion of a geopolymer layer to a geopolymer substrate and a concrete substrate are presented. As a result of this study, a higher adhesion strength of the geopolymer layer to the geopolymer substrate was found in comparison to geopolymer coatings applied on conventional concrete. Adhesion tests were also conducted for steel substrates to which both geopolymer and acrylic lacquer were applied.

An Overview of Common Infrared Techniques for Detecting CO Intermediates on Metal Surfaces for Hydrocarbon Products

Detection of intermediates during the catalytic process by infrared techniques has been widely implemented for many important reactions. For the reduction of CO2 into hydrocarbons on metal surfaces, CO molecule is one of the most important transient species to be followed due to its involvement in several products’ pathways, and its distinct vibrational features. Herein, basic understandings behind these utilized infrared techniques are illustrated aiming for highlighting the potential of each infrared technique and its advantages over the other ones for detecting CO molecules on metal surfaces.