Unveiling the Interfacial and Structural Heterogeneity of Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene Etched with CoF<sub>2</sub>/HCl by Integrated <i>in Situ</i> Thermal Analysis
Cody B. Cockreham, Xianghui Zhang, Jeffrey A. Eakin, Martinus Dewa, Houqian Li, Nan Li, Junming Sun, Su Ha, Cornelius F. Ivory, Yong Wang, Hongwu Xu, Di Wu
Abstract
Ti3C2Tx MXene is a member of the recently discovered two-dimensional early transition metal carbide and nitride family of MXenes with potential applications in energy storage and heterogeneous catalysis at elevated temperatures. Here, we apply a suite of in situ techniques to probe Ti3C2Tx MXene’s thermal evolutions, including in situ X-ray diffraction (XRD), in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), and integrated thermogravimetry–differential scanning calorimetry–mass spectrometry (TG-DSC-MS). In light of this set of in situ investigations, we find heterogeneity in the layering of Ti3C2Tx MXene revealed only at higher temperatures. Our findings present behavior up to 600 °C, particularly interlayer water and −OH surface end-capping groups. In one group of layers, their interlayer spacing shrinks as water deintercalates, but the other group of layers unexpectedly shows no change in the interlayer spacing. This is strong evidence that intercalants act as guest pillaring agents in the latter layering group, which stabilize these layers at higher temperatures while keeping the interlayer space accessible.