No abstract

2D transition metal carbides and nitrides (MXenes), a class of emerging nanomaterials with intriguing properties, have attracted significant attention in recent years. However, owing to the highly hydrophilic nature of MXene nanosheets, assembly strategies of MXene at liquid–liquid interfaces have been very limited and challenging. Herein, through the cooperative assembly of MXene and amine‐functionalized polyhedral oligomeric silsesquioxane at the oil–water interface, we report the formation, assembly, and jamming of a new type MXene‐based Janus‐like nanoparticle surfactants, termed MXene‐surfactants (MXSs), which can significantly enhance the interfacial activity of MXene nanosheets. More importantly, this simple assembly strategy opens a new platform for the fabrication of functional MXene assemblies from mesoscale (e.g., structured liquids) to macroscale (e.g., aerogels), that can be used for a range of applications, including nanocomposites, electronic devices, and all‐liquid microfluidic devices.

Although hydrophilic and electrically conductive transition-metal carbon/nitride (MXenes) nanosheets hold great promise for electrically conductive and electromagnetic interference (EMI) shielding applications, the weak interaction among MXene nanosheets makes them difficult to form compressible three-dimensional architectures with high conductivity. Herein, inspired by the plant “Parthenocissus tricuspidata”, an efficient approach is demonstrated to fabricate conductive and lightweight Ti3C2T x MXene/acidified carbon nanotube anisotropic aerogels (MCAs) with superelasticity and high thermal insulation. The MXene nanosheets construct the anisotropic and porous skeleton, while the acidified carbon nanotubes reinforce the pore walls of MXene nanosheets, making the MCAs superelastic and compressible. The superelastic MCA with only 5 wt % of the acidified carbon nanotubes is structurally stable during cyclic compressions at both high and ultralow temperatures. Its high conductivity (447.2 S m–1) and ultralow density (9.1 mg cm–3) endow its paraffin composite with a high EMI shielding efficiency of ∼51 dB at an ultralow filler content of 0.3 vol %. When the density of MCA increases to 18.2 mg cm–3, its EMI shielding effectiveness reaches 90 dB. Additionally, the porous and ultralight MCAs exhibit better thermal insulation performances as compared to commercial melamine and polystyrene foams. Therefore, the superelastic, electrically conductive, lightweight, and thermally insulating MCAs would be promising for EMI shielding applications in space equipment and portable wearable devices.

Highlights 3D printing of MXene frames with tunable electromagnetic interference shielding efficiency is demonstrated. Highly conductive MXene frames are reinforced by cross-linking with aluminum ions. Electromagnetic wave is visualized by electromagnetic-thermochromic MXene patterns. Abstract The highly integrated and miniaturized next-generation electronic products call for high-performance electromagnetic interference (EMI) shielding materials to assure the normal operation of their closely assembled components. However, the most current techniques are not adequate for the fabrication of shielding materials with programmable structure and controllable shielding efficiency. Herein, we demonstrate the direct ink writing of robust and highly conductive Ti3C2Tx MXene frames with customizable structures by using MXene/AlOOH inks for tunable EMI shielding and electromagnetic wave-induced thermochromism applications. The as-printed frames are reinforced by immersing in AlCl3/HCl solution to remove the electrically insulating AlOOH nanoparticles, as well as cross-link the MXene sheets and fuse the filament interfaces with aluminum ions. After freeze-drying, the resultant robust and porous MXene frames exhibit tunable EMI shielding efficiencies in the range of 25–80 dB with the highest electrical conductivity of 5323 S m−1. Furthermore, an electromagnetic wave-induced thermochromic MXene pattern is assembled by coating and curing with thermochromic polydimethylsiloxane on a printed MXene pattern, and its color can be changed from blue to red under the high-intensity electromagnetic irradiation. This work demonstrates a direct ink printing of customizable EMI frames and patterns for tuning EMI shielding efficiency and visualizing electromagnetic waves.

Using pulsed laser deposition, YBa2Cu3O7−δ (YBCO) films ranging in thickness from 0.065 to 6.4 μm have been deposited on yttria-stabilized zirconia substrates with an intermediate layer of CeO2. The thinnest films have critical current densities of over 5 MA/cm2 at 75 K with zero applied field; as film thickness is increased, Jc decreases asymptotically to 1 MA/cm2. X-ray analysis of a 2.2-μm-thick film shows that the YBCO is predominantly c-axis oriented and textured in-plane, while a Rutherford backscattering spectrometry minimum channeling yield of ≊75% indicates that the film contains disordered material at this thickness.