A DFT Study of Catechol Polymer Adhesion onto γ-Alumina (110) Surfaces

The adhesion mechanism of catechol, a key functional group in marine bioadhesives, to dehydroxylated γ-alumina (γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup>) (110) and hydroxylated (γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup>) (110) surfaces was investigated using periodic density functional theory (DFT) calculations. Adhesion interface models were constructed by integrating catechol, modeled after the experimentally synthesized poly(3,4-dihydroxystyrene), with γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surfaces, referred to as the catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) interfaces. Stable catechol-surface complexes, adhesion energies, and interaction sites were identified through DFT-based geometric optimizations of selected models. DFT calculations revealed that hydroxy groups of catechol interact with both γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surfaces, with charge density difference (CDD) and crystal orbital Hamilton population (COHP) analysis highlighting hydrogen bonding as the predominant and robust interaction at both interfaces. Adhesive forces were computed by differentiating energy curves obtained through the vertical displacement of the catechol from the adherend surfaces. The results revealed that the adhesive force on the catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) interface is more substantial than on the catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) interface. The adhesive force, decomposed into DFT and dispersion components, showed a pronounced contribution from the DFT component at both interfaces. Furthermore, the catechol structures, with truncated hydroxy hydrogen atoms achieved by stretching O-H bonds, adsorbed on the γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surfaces were obtained as the models of chemisorption and physisorption, respectively. On the γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) surface, catechol is converted into semiquinone in correspondence with a chemical reaction involving chemisorption, proton transfer, and the associated electron transfer. As a result of these interaction modes, the adhesive force is significantly higher compared to the structure, where catechol's hydroxy groups remain intact, with an energy of -233.5 kJ/mol per surface model. In contrast, catechol adsorption on the γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surface occurs mainly by physisorption via hydrogen bonding.

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Publication Details

Journal
Langmuir
Published
2025-08-25
DOI
https://doi.org/10.1021/acs.langmuir.5c02791
Citations
4
Primary Topic
Polymer Surface Interaction Studies
Type
article
Field-Weighted Citation Impact
2.64

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article

A DFT Study of Catechol Polymer Adhesion onto γ-Alumina (110) Surfaces

Kazunari Yoshizawa, Kotaro Satoh, Yoshihito Shiota, Ken Kojio et al.
4 citations
Langmuir
Polymer Surface Interaction Studies
2.64
article

A DFT Study of Catechol Polymer Adhesion onto γ-Alumina (110) Surfaces

Kazunari Yoshizawa, Kotaro Satoh, Yoshihito Shiota, Ken Kojio, Satoru Yamamoto, Amit Shrestha, Keiji Tanaka
article en
4 citations

Abstract

The adhesion mechanism of catechol, a key functional group in marine bioadhesives, to dehydroxylated γ-alumina (γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup>) (110) and hydroxylated (γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup>) (110) surfaces was investigated using periodic density functional theory (DFT) calculations. Adhesion interface models were constructed by integrating catechol, modeled after the experimentally synthesized poly(3,4-dihydroxystyrene), with γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surfaces, referred to as the catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) interfaces. Stable catechol-surface complexes, adhesion energies, and interaction sites were identified through DFT-based geometric optimizations of selected models. DFT calculations revealed that hydroxy groups of catechol interact with both γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surfaces, with charge density difference (CDD) and crystal orbital Hamilton population (COHP) analysis highlighting hydrogen bonding as the predominant and robust interaction at both interfaces. Adhesive forces were computed by differentiating energy curves obtained through the vertical displacement of the catechol from the adherend surfaces. The results revealed that the adhesive force on the catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) interface is more substantial than on the catechol/γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) interface. The adhesive force, decomposed into DFT and dispersion components, showed a pronounced contribution from the DFT component at both interfaces. Furthermore, the catechol structures, with truncated hydroxy hydrogen atoms achieved by stretching O-H bonds, adsorbed on the γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) and γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surfaces were obtained as the models of chemisorption and physisorption, respectively. On the γ-Al<sub>2</sub>O<sub>3</sub><sup>D</sup> (110) surface, catechol is converted into semiquinone in correspondence with a chemical reaction involving chemisorption, proton transfer, and the associated electron transfer. As a result of these interaction modes, the adhesive force is significantly higher compared to the structure, where catechol's hydroxy groups remain intact, with an energy of -233.5 kJ/mol per surface model. In contrast, catechol adsorption on the γ-Al<sub>2</sub>O<sub>3</sub><sup>H</sup> (110) surface occurs mainly by physisorption via hydrogen bonding.

LangmuirVol. 41(35)
Kyushu University (JP), Kyoto University (JP)
Japan Society for the Promotion of Science, JST-Mirai Program
Openalex Percentile: Top 10%
Polymer Surface Interaction Studies
2.64
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