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Study of the impact of etching mixtures on the surface chemistry and electrocatalytic activity of multilayer Ti3C2Tx MXenes
Departamento de Ingeniería Química, Tecnológico Nacional de México, Instituto Tecnológico de Celaya, Avenida Tecnológico esq., A. García Cubas #600 Pt, Guanajuato, Celaya, Mexico.
Cátedras-CONACYT CINVESTAV, Mérida Km 6, Carretera Antigua a Progreso, Cordemex, Yucatán, Mérida, Mexico.
Umeå University, Faculty of Science and Technology, Department of Physics.ORCID iD: 0000-0001-9239-0541
LINAN-IPICYT, Camino a La Presa San José 2055. Col. Lomas 4 Sección, San Luis Potosí, Mexico.
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2026 (English)In: Next Materials, E-ISSN 2949-8228, Vol. 13, article id 103598Article in journal (Refereed) Published
Abstract [en]

Ti₃C₂Tₓ MXenes are commonly obtained through the chemical etching of the Ti₃AlC₂ MAX phase; however, the influence of the composition of the etching medium on their physicochemical properties and electrocatalytic performance requires further detailed understanding. This study comparatively evaluates the effect of three fluorine-based etching systems (HF, HF–LiCl, and HF–HCl) on the structure, surface chemistry, and electrocatalytic activity of multilayered MXenes. The main contribution of this study is establishing a relationship between the etching medium composition, the structural and surface modifications of Ti₃C₂Tₓ, and its response applied to the hydrogen evolution reaction (HER). The results showed that incorporating LiCl and HCl into the HF medium significantly modifies the Al removal process and the final characteristics of the MXene. In particular, the HF–LiCl and HF–HCl systems facilitate more efficient Al removal and produce more homogeneous morphologies than concentrated HF. Furthermore, the HF–HCl system yields greater interlayer spacing and a higher presence of Ti–O and Ti–OH functional groups, thereby enhancing active site accessibility and charge transfer. These modifications impacted directly the electrochemical performance since the MXene obtained using HF–HCl exhibits the highest HER activity, associated with a larger electrochemically active surface area and lower charge-transfer resistance. Overall, the results demonstrated that the chemistry of the etching medium is a decisive parameter for simultaneously controlling the structure, surface chemistry, and electrocatalytic behavior of Ti₃C₂Tₓ. These findings highlight the importance of optimizing synthesis conditions as a materials engineering strategy to obtain MXenes with tailored properties for energy conversion and electrocatalysis applications.

Place, publisher, year, edition, pages
Elsevier, 2026. Vol. 13, article id 103598
Keywords [en]
Etching chemistry, Hydrogen evolution reaction (HER), Surface functionalization, Ti₃C₂Tₓ MXenes
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:umu:diva-259326DOI: 10.1016/j.nxmate.2026.103598Scopus ID: 2-s2.0-105051162012OAI: oai:DiVA.org:umu-259326DiVA, id: diva2:2107339
Available from: 2026-10-02 Created: 2026-10-02 Last updated: 2026-10-02Bibliographically approved

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Gracia-Espino, EduardoPuentes-Prado, Laura ElenaKuzhikandathil Mohamed, AliceRafei, Mouna

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1920212223242522 of 264
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