Agent free pillaring engineering of interlayer spacing of Ti3C2 MXene layers for energy conversion and photothermal desalination

IF 13.2 1区 工程技术 Q1 ENGINEERING, CHEMICAL
Min Wei Boey, Muhammad Ahmad, Jiawei Sun, Sai Kishore Ravi, Xue Wang, Muhammad Usman Farid, Alicia Kyoungjin An
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Abstract

The interlayer stacking of two-dimensional (2D) nanomaterials hinders their application in energy-related fields. This work introduces a unique yet simple strategy to enhance the interlayer spacing of T3C2 MXene layers without adding foreign pillaring agents, using an in situ oxidation method. This strategy converts surface titanium into titanium oxide, which acts as a pillaring agent between the single layers while retaining the inherent 2D layered structure of MXene. This modification enhances the interlayer spacing and provides highly active centers of titanium oxide. Morphological and structural analyses confirm the formation of titanium oxide active centers and the consequent increase in interlayer spacing, making the material a more effective photocatalyst for CO2 reduction and enabling simultaneous desalination through photothermal evaporation. The optimized in situ oxidized sample, TixO2(T3-xC2), outperforms pristine MXene by achieving a high solar desalination rate of 1.51 kg m−2 h−1 with a thermal efficiency of 85.3%. Additionally, under one-sun irradiation, the TixO2(T3-xC2) membrane exhibits a CO evolution rate of 60.67 μmol m−2 h−1. The superior photothermal effect and photocatalytic activity, compared to intrinsic MXene layers, are attributed to the higher interlayer spacing, which increases ionic conductivity, exposes titanium oxide metal active centers, and provides more active sites.
Ti3C2 MXene层间间距无剂支撑工程用于能量转换和光热脱盐
二维纳米材料的层间堆积阻碍了其在能源相关领域的应用。本文介绍了一种独特而简单的方法,在不添加外来柱状剂的情况下,利用原位氧化法提高T3C2 MXene层间间距。该策略将表面钛转化为氧化钛,氧化钛作为单层之间的支柱剂,同时保留了MXene固有的二维层状结构。这种改性提高了层间距,并提供了高活性的氧化钛中心。形态和结构分析证实了氧化钛活性中心的形成以及层间间距的增加,使该材料成为更有效的二氧化碳还原光催化剂,并通过光热蒸发实现同时脱盐。优化后的原位氧化样品TixO2(T3-xC2)的太阳能脱盐率为1.51 kg m−2 h−1,热效率为85.3%,优于原始MXene。此外,在一次太阳照射下,TixO2(T3-xC2)膜的CO演化速率为60.67 μmol m−2 h−1。与MXene层相比,其优越的光热效应和光催化活性是由于层间间距较大,增加了离子电导率,暴露了氧化钛金属活性中心,并提供了更多的活性位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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