MXenes are recently discovered two-dimensional materials which have shown great promise in electrochemical energy storage. However, the majority of research has been on lithium and sodium systems, with little work done on multivalent ion systems, which have an urgent need for new electrode materials. In particular, zinc-ion aqueous systems have significant promise due to the widespread use of zinc batteries and the abundance (24th most abundant element on earth), high specific capacity (> 800 mAh g -1 ) and low toxicity of zinc. Only a few materials are reported to act as reversible zinc-ion hosts, hindering developments of this technology. In this work, we demonstrate for the first time that Ti3C2, the most studied MXene to date, can act as a reversible zinc-ion host for a hybrid capacitor using an aqueous zinc sulphate electrolyte. In addition, we report a novel in-situ pillaring method where CTAB is used to increase the Zn-ion uptake, with capacities up to 189 mAh g -1 .A detailed mechanistic study that encompasses diffraction, microscopy and spectroscopy techniques was conducted to shed light on the structure and kinetics of the system. This understanding was used to optimise the electrode performance, resulting in an outstanding cycling stability of over 96% over 1,000 cycles. We believe this study will pave the pathway towards designing new pillared MXenes in low-cost Zn-ion aqueous systems.

Here we report direct physical evidence that confinement of molecular hydrogen (H2) in an optimized nanoporous carbon results in accumulation of hydrogen with characteristics commensurate with solid H2 at temperatures up to 67 K above the liquid-vapor critical temperature of bulk H2. This extreme densification is attributed to confinement of H2 molecules in the optimally sized micropores, and occurs at pressures as low as 0.02 MPa. The quantities of contained, solid-like H2 increased with pressure and were directly evaluated using in situ inelastic neutron scattering and confirmed by analysis of gas sorption isotherms. The demonstration of the existence of solid-like H2 challenges the existing assumption that supercritical hydrogen confined in nanopores has an upper limit of liquid H2 density. Thus, this insight offers opportunities for the development of more accurate models for the evaluation and design of nanoporous materials for high capacity adsorptive hydrogen storage.

Energy storage is a global critical issue and important area of research as most of the renewable sources of energy are intermittent. In this research work, recently emerged inorganic nanomaterial (MXene) is used for the first time with paraffin wax as a phase change material (PCM) to improve its thermo-physical properties. This paper focuses on preparation, characterization, thermal properties and thermal stability of new class of nanocomposites induced with MXene nanoparticles in three different concentrations. Acquired absorbance (UV-Vis) for nanocomposite with loading concentration of 0.3 wt.% of MXene achieved ~39% enhancement in comparison with the pure paraffin wax. Thermal conductivity measurement for nanocomposites in a solid state is performed using a KD2 PRO decagon. The specific heat capacity (c p ) of PCM based MXene is improved by introducing MXene. The improvement of c p is found to be 43% with 0.3 wt.% of MXene loaded in PCM. The highest thermal conductivity increment is found to be 16% at 0.3 wt.% concentration of MXene in PCM. Decomposition temperature of this new class of nanocomposite with 0.3 wt.% mass fraction is increased by ~6%. This improvement is beneficial in thermal energy storage and heat transfer applications.

In this work, we apply an amine-assisted silica pillaring method to create the first example of a porous Mo2TiC2 MXene with nanoengineered interlayer distances. The pillared Mo2TiC2 has a surface...

MXenes are a recently discovered class of two-dimensional materials that have shown great potential as electrodes in electrochemical energy storage devices. Despite their promise in this area, MXenes can still suffer limitations in the form of restricted ion accessibility between the closely spaced multistacked MXene layers causing low capacities and poor cycle life. Pillaring, where a secondary species is inserted between layers, has been used to increase interlayer spacings in clays with great success but has had limited application in MXenes. We report a new amine-assisted pillaring methodology that successfully intercalates silica-based pillars between Ti 3 C 2 layers. Using this technique, the interlayer spacing can be controlled with the choice of amine and calcination temperature, up to a maximum of 3.2 nm, the largest interlayer spacing reported for an MXene. Another effect of the pillaring is a dramatic increase in surface area, achieving BET surface areas of 235 m 2 g –1 , a sixty-fold increase over the unpillared material and the highest reported for MXenes using an intercalation-based method. The intercalation mechanism was revealed by different characterization techniques, allowing the surface chemistry to be optimized for the pillaring process. The porous MXene was tested for Na-ion battery applications and showed superior capacity, rate capability and remarkable stability compared with those of the nonpillared materials, retaining 98.5% capacity between the 50th and 100th cycles. These results demonstrate the applicability and promise of pillaring techniques applied to MXenes providing a new approach to optimizing their properties for a range of applications, including energy storage, conversion, catalysis, and gas separations.