Synthesis and Surface Chemistry of 2D TiVC Solid-Solution MXenes

MXenes are emerging two-dimensional (2D) materials for energy-storage applications and supercapacitors. Their surface chemistry, which determines critical properties, varies due to different synthesis conditions. In this work, we synthesized TiVC solid-solution MXenes by two different synthesis methods and investigated their surface functional groups. We performed etching of the TiVAlC MAX phase using two different solutions, a highly concentrated HF (50 wt % ≈ 29 M) and a mixture of LiF and HCl (1.9 M LiF/12 M HCl). Large-scale delamination of TiVCT_x to produce single-flake suspension was achieved by further intercalation of the resultant MXene from LiF/HCl with tetrabutylammonium hydroxide (TBAOH). X-ray diffraction indicates a large interlayer spacing of 2.18 nm for TiVCT_x MXene flakes. To investigate the structural stability and adsorption energy of different functional groups on TiVC MXenes, density functional theory (DFT) calculations were performed and supported with X-ray photoelectron spectroscopy (XPS) measurements. A higher concentration of ═O and a lower concentration of -F were achieved on the TiVC synthesized by LiF/HCl, both of which provide a more favorable surface chemistry for energy-storage applications. Our results provide the first systematic study on the effect of synthesis conditions on the surface chemistry of solid-solution TiVC MXenes.