{"title":"Reliance of MXene terminating groups on various synthetic strategies and its hot electron dynamics at MXene interfaces","authors":"Pei Zhang , Qi Zheng , Tariq Bashir , Tariq Ali , Sikandar Khan , Asma M. Alenad , Saleem Raza","doi":"10.1016/j.jece.2024.114708","DOIUrl":null,"url":null,"abstract":"<div><div>MXenes are two-dimensional (2D) materials with notable properties, attracting significant attention. These materials are often synthesized with surface functionalization like -O, -OH, and -F, which regulate their properties. While experimental synthesis typically results in mixed terminations, computational studies predict pure terminations. This study provides a comprehensive overview of the characteristics and potential applications of chemical termination in MXenes. The type of terminating groups depends on the fabrication media: aqueous media yields -OH and -O terminations, alkaline media yields -F, -Cl, -Br, and -I, ammonium bifluoride etching yields -NH<sup>4+</sup> and NH<sub>3</sub>, and direct synthesis methods yield various terminations on demand. We also explore the role of photo-induced non-thermalized heated electrons at interfaces in plasmonic-driven chemical processes. Understanding these electron dynamics, which occur before thermalization (∼125 fs), remains challenging. Femtosecond time-resolved spectroscopy was used to study these dynamics in MXene/molecule complexes. This technique allows distinguishing between thermalized and non-thermalized electron responses. There are two non-thermalization channels: (i) rapid transport of non-heated electrons to attached molecules in less than 50 fs, and (ii) heating of adsorbed molecules due to non-thermalized electron scattering within 125 fs. These paths depend on the irradiating wavelength and the energy differential between molecules and MXene. Computational predictions of thermodynamically stable MXene compositions are essential for directing experimental goals. This work also presents a thorough computational investigation for thermodynamically stable MXenes with 11 surface terminating groups. The analysis of results investigates factors essential for assessing the thermodynamic stability of MXenes, revealing that the chemistry of MXene surface terminations is significantly crucial to hot electron dynamics and thermodynamic stability. This review also offers insights into the MXene termination process, synthesis media, and synthetic strategies, highlighting the importance of intercalation process. It also elucidates mechanisms and opportunities in hot electron theory, interfacial heat transfer, and photocatalysis.</div></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":"12 6","pages":"Article 114708"},"PeriodicalIF":7.4000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Environmental Chemical Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213343724028409","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
MXenes are two-dimensional (2D) materials with notable properties, attracting significant attention. These materials are often synthesized with surface functionalization like -O, -OH, and -F, which regulate their properties. While experimental synthesis typically results in mixed terminations, computational studies predict pure terminations. This study provides a comprehensive overview of the characteristics and potential applications of chemical termination in MXenes. The type of terminating groups depends on the fabrication media: aqueous media yields -OH and -O terminations, alkaline media yields -F, -Cl, -Br, and -I, ammonium bifluoride etching yields -NH4+ and NH3, and direct synthesis methods yield various terminations on demand. We also explore the role of photo-induced non-thermalized heated electrons at interfaces in plasmonic-driven chemical processes. Understanding these electron dynamics, which occur before thermalization (∼125 fs), remains challenging. Femtosecond time-resolved spectroscopy was used to study these dynamics in MXene/molecule complexes. This technique allows distinguishing between thermalized and non-thermalized electron responses. There are two non-thermalization channels: (i) rapid transport of non-heated electrons to attached molecules in less than 50 fs, and (ii) heating of adsorbed molecules due to non-thermalized electron scattering within 125 fs. These paths depend on the irradiating wavelength and the energy differential between molecules and MXene. Computational predictions of thermodynamically stable MXene compositions are essential for directing experimental goals. This work also presents a thorough computational investigation for thermodynamically stable MXenes with 11 surface terminating groups. The analysis of results investigates factors essential for assessing the thermodynamic stability of MXenes, revealing that the chemistry of MXene surface terminations is significantly crucial to hot electron dynamics and thermodynamic stability. This review also offers insights into the MXene termination process, synthesis media, and synthetic strategies, highlighting the importance of intercalation process. It also elucidates mechanisms and opportunities in hot electron theory, interfacial heat transfer, and photocatalysis.
期刊介绍:
The Journal of Environmental Chemical Engineering (JECE) serves as a platform for the dissemination of original and innovative research focusing on the advancement of environmentally-friendly, sustainable technologies. JECE emphasizes the transition towards a carbon-neutral circular economy and a self-sufficient bio-based economy. Topics covered include soil, water, wastewater, and air decontamination; pollution monitoring, prevention, and control; advanced analytics, sensors, impact and risk assessment methodologies in environmental chemical engineering; resource recovery (water, nutrients, materials, energy); industrial ecology; valorization of waste streams; waste management (including e-waste); climate-water-energy-food nexus; novel materials for environmental, chemical, and energy applications; sustainability and environmental safety; water digitalization, water data science, and machine learning; process integration and intensification; recent developments in green chemistry for synthesis, catalysis, and energy; and original research on contaminants of emerging concern, persistent chemicals, and priority substances, including microplastics, nanoplastics, nanomaterials, micropollutants, antimicrobial resistance genes, and emerging pathogens (viruses, bacteria, parasites) of environmental significance.