Energy and environmental issues presently attract a great deal of scientific attention. Recently, two-dimensional MXenes and MXene-based nanomaterials have attracted increasing interest because of their unique properties (e.g., remarkable safety, a very large interlayer spacing, environmental flexibility, a large surface area, and thermal conductivity). In 2011, multilayered MXenes (Ti₃C₂T_x, a new family of two-dimensional (2D) materials) produced by etching an A layer from a MAX phase of Ti₃AlC₂, were first described by researchers at Drexel University. The term “MXene” was coined to distinguish this new family of 2D materials from graphene, and applies to both the original MAX phases and MXenes fabricated from them. We present a comprehensive review of recent studies on energy and environmental applications of MXene and MXene-based nanomaterials, including energy conversion and storage, adsorption, membrane, photocatalysis, and antimicrobial. Future research needs are discussed briefly with current challenges that must be overcome before we completely understand the extraordinary properties of MXene and MXene-based nanomaterials.

This paper reports the results of an international interlaboratory study led by the National Institute of Standards and Technology (NIST) on the measurement of high-pressure surface excess carbon dioxide adsorption isotherms on NIST Reference Material RM 8852 (ammonium ZSM-5 zeolite), at 293.15 K (20 °C) from 1 kPa up to 4.5 MPa. Eleven laboratories participated in this exercise and, for the first time, high-pressure adsorption reference data are reported using a reference material. An empirical reference equation \({n_{ex}}=\frac{d}{{{{(1+\exp [\left( { - {\text{ln}}(P)+a} \right)/b~])}^{c~~}}}}~,\) [n_ex-surface excess uptake (mmol/g), P-equilibrium pressure (MPa), a = −6.22, b = 1.97, c = 4.73, and d = 3.87] along with the 95% uncertainty interval (U_k = 2 = 0.075 mmol/g) were determined for the reference isotherm using a Bayesian, Markov Chain Monte Carlo method. Together, this zeolitic reference material and the associated adsorption data provide a means for laboratories to test and validate high-pressure adsorption equipment and measurements. Recommendations are provided for measuring reliable high-pressure adsorption isotherms using this material, including activation procedures, data processing methods to determine surface excess uptake, and the appropriate equation of state to be used.

Integrated metal–organic frameworks (MOFs) with graphene oxide (GO) have aroused huge interest in recent years due to their unique properties and excellent performance compared to MOFs or GO alone. While a lot of attention has been focused on the synthesis methodologies and the performance analysis of the composite materials in recent years, the fundamental formation/crystallization mechanism(s) is (are) still not fully understood. Ascribed to the distinctive structural and functional properties of GO, the nucleation and crystallization process of MOFs could be altered/promoted, forming MOF/GO composite materials with different nanostructures. Furthermore, the MOF’s parental structure could also influence how the GO and MOF bond together. Thus, this short review attempted to provide critical and indepth discussions of recent research results with a particular focus on the factors that influence the directional growth of parent MOFs in the presence of graphene oxide. Due to the unique structure and enhanced properties, the derived MOF/GO composites have a wide range of applications including gas separation, electrochemistry, and photocatalysis. We hope this review will be of interest to researchers working on MOF design, crystal structure control (e.g., orientation), and composite materials development.