Kinetics of the electrochemically-assisted deposition of sol–gel films

Literature Information

Publication Date 2017-05-16
DOI 10.1039/C7CP01775H
Impact Factor 3.676
Authors

Liang Liu, Alain Walcarius


View Original

Abstract

Electrochemically-assisted deposition is now becoming a widespread method for preparing sol–gel films. It is based on the electrochemical generation of OH− ions, which can then catalyze the sol–gel condensation reactions. It has a key advantage of selectively facilitating the film deposition on electrochemically active surfaces while not affecting the stability of the bulk precursor solution. Experimental studies have clearly shown that the thickness of the electrochemically-assisted deposited films is influenced by the deposition parameters such as the potential and time. However, there is still a lack of quantitative description of the kinetics of film growth due to the complexity of the process. In this preliminary study, we derived quantitative analytical expressions for describing the kinetics associated with the growth of sol–gel films generated by electrochemically assisted deposition. Both heterogeneous and homogeneous condensation reactions were considered. The key strategy was to simplify the process by separating the electrochemical step of generating OH− ions with the condensation steps of film formation under approximation. Furthermore, numerical simulation was carried out to examine the validity and any errors in the analytical expressions in the cases when the required approximations were not fulfilled. The analytical expressions could well explain the trends observed in the experimental studies and could also be used for fitting the experimental results from the literature. This study provides a deeper understanding of the mechanism and quantitative guidance for manipulating electrochemically-assisted deposition processes at a large scale in industry. It may also be referred to in regard to other indirect electrodeposition systems in which the deposition is not an electrochemical step but is instead driven by electrochemically-generated catalysts.

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Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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