First-Principles Calculations on the Adsorption Behavior of Amino Acids on a Titanium Carbide MXene

José D Gouveia; Gerard Novell-Leruth; Pedro M L S Reis; Francesc Viñes; Francesc Illas; José R B Gomes

doi:10.1021/acsabm.0c00621

First-Principles Calculations on the Adsorption Behavior of Amino Acids on a Titanium Carbide MXene

ACS Appl Bio Mater. 2020 Sep 21;3(9):5913-5921. doi: 10.1021/acsabm.0c00621. Epub 2020 Aug 19.

Authors

José D Gouveia¹, Gerard Novell-Leruth¹, Pedro M L S Reis¹, Francesc Viñes², Francesc Illas², José R B Gomes¹

Affiliations

¹ Department of Chemistry, CICECO-Aveiro Institute of Materials, University of Aveiro, Campus Universitário de Santiago, Aveiro 3810-193, Portugal.
² Departament de Ciència de Materials i Quı́mica Fı́sica & Institut de Quı́mica Teòrica i Computacional (IQTCUB), Universitat de Barcelona, c/Martı́ i Franqués 1, 08028 Barcelona, Spain.

PMID: 35021819
DOI: 10.1021/acsabm.0c00621

Abstract

Due to their vast range of promising biomedical and electronic applications, there is a growing interest in bioinorganic lamellar nanomaterials. MXenes are one such class of materials, which stand out by virtue of their demonstrated biocompatibility, pharmacological applicability, energy storage performance, and feasibility as single-molecule sensors. Here, we report on first-principles predictions, based on density functional theory, of the binding energies and ground-state configurations of six selected amino acids (AAs) adsorbed on O-terminated two-dimensional titanium carbide, Ti₂CO₂. We find that most AAs (aspartic acid, cysteine, glycine, and phenylalanine) prefer to adsorb via their nitrogen atom, which forms a weak bond with a surface Ti atom, with bond lengths of around 2.35 Å. In contrast, histidine and serine tend to adsorb parallel to the MXene surface, with their α carbon about 3 Å away from it. In both adsorption configurations, the adsorption energies are on the order of the tenths of an electronvolt. In addition, we find a positive, nearly linear correlation between the binding energy of each studied AA and its van der Waals volume, which suggests an adsorption dominated by van der Waals forces. This relationship allowed us to predict the adsorption energies for all of the proteinogenic AAs on the same Ti₂CO₂ MXene. Our analysis additionally shows that in the parallel adsorption mode there is a negligible transfer of charge density from the AA to the surface but noticeable in the N-bonded adsorption mode. In the latter, the isosurfaces of charge density differences show accumulation of shared electrons in the region between N and Ti, confirming the predicted N-Ti bond. The moderate adsorption energy values calculated, as well as the preservation of the integrity of both the AAs and the surface upon adsorption, reinforce the capability of Ti₂CO₂ as a promising reusable biosensor for amino acids.

Keywords: 2D materials; adsorption; amino acid; biosensors; clean MXenes; density functional theory; titanium carbide.