MXene, an advanced family of 2D ceramic material resembling graphene, has had a considerable impact on the field of research because of its unique physiochemical properties. MXene has been synthesized by the selective etching of MAX via different techniques. However, with the passage of time, due to the need for further progress and improvement in MXene materials, ideas have turned toward composite fabrication, which has aided boosting the MXene composites regarding their properties and applications in various areas. Many review papers are published on MXene and their composites with polymer, carbon nanotube, graphene, other carbon, metal oxides and sulfides, etc., except metal composite, and such papers discuss these composites thoroughly. In this review article, we illustrate and explain the development of MXene-based metal composites. Furthermore, we highlight the synthesis techniques utilized for the preparation of MXene composites with metal. We briefly discuss the enhancement of properties of the composites and a wide range of applications as an electrode substance for energy storage devices, electrochemical cells, supercapacitors, and catalytic and anti-corrosive performance. Major obstacles in MXene and metal composite are mentioned and provide future recommendations. Together, they can overcome problems and enable MXene and composites on commercial-scale production.

In this study, a Al₂O₃–ZrO₂–SiO2 slurry was prepared as a coating material, which formed an alumina–zirconia–mullite composite coating after sintering. A zirconia substrate was coated using the alumina–zirconia–mullite composite in order to enhance its strengthviacompressive residual stress.

In the present study, the dense Cr and Cr_0.92Si_0.08 coatings have been deposited on Zircaloy-4 substrates by the magnetron sputtering technique. The high-temperature oxidation resistance of coatings is evaluated in 1200 °C steam for 1–4 h. The Cr_0.92Si_0.08 coating shows better oxidation resistance than the Cr coating. The in-situ formed Zr₂Si diffusion barrier inhibits the mutual diffusion of Cr and Zr. And the formation of a Cr₂O₃/SiO₂ double-layer scale effectively improves the oxidation resistance of a single Cr₂O₃ layer. The formation of the in-situ diffusion barrier, Cr₂O₃/SiO₂ scales and oxidation protection mechanisms of the Cr_0.92Si_0.08 coating have been discussed in detail.

The accurate evaluation of the elastic modulus of ceramic coatings at high temperature (HT) is of high significance for industrial application, yet it is not easy to get the practical modulus at HT due to the difficulty of the deformation measurement and coating separation from the composite samples. This work presented a simple approach in which relative method was used twice to solve this problem indirectly. Given a single-face or double-face coated beam sample, the relative method was firstly used to determine the real mid-span deflection of the three-point bending piece at HT, and secondly to derive the analytical relation among the HT moduli of the coating, the coated and uncoated samples. Thus the HT modulus of the coatings on beam samples is determined uniquely via the measured HT moduli of the samples with and without coatings. For a ring sample (from tube with outer-side, inner-side, and double-side coating), the relative method was used firstly to determine the real compression deformation of a split ring sample at HT, secondly to derive the relationship among the slope of load-deformation curve of the coated ring, the HT modulus of the coating and substrate. Thus, the HT modulus of ceramic coatings can be evaluated by the substrate modulus and the load-deformation data of coated rings. Mathematic expressions of those calculations were derived for the beam and ring samples. CVD-SiC coatings on graphite substrate were selected as the testing samples, of which the measured modulus ranging from room temperature to 2100 °C demonstrated the validity and convenience of the relative method.