MXene has shown enormous potential in scientific fields, including energy storage and electromagnetic interference (EMI) shielding. Unfortunately, MXene-based material structures generally suffer from mechanical fragility and vulnerability to oxidation. Herein, musselinspired dopamine successfully addresses those weaknesses by improving interflake interaction and ordering in MXene assembled films. Dopamine undergoes in situ polymerization and binding at MXene flake surfaces by spontaneous interfacial charge transfer, yielding an ultrathin adhesive layer. Resultant nanocomposites with highly aligned tight layer structures achieve approximately seven times enhanced tensile strength with a simultaneous increase of elongation. Ambient stability of MXene films is also greatly improved by the effective screening of oxygen and moisture. Interestingly, angstrom thick polydopamine further promotes the innate high electrical conductivity and excellent EMI shielding properties of MXene films. This synergistic concurrent enhancement of physical properties proposes MXene/polydopamine hybrids as a general platform for MXene based reliable applications.

Hybridization of low-dimensional components with diverse geometrical dimensions should offer an opportunity for the discovery of synergistic nanocomposite structures. In this regard, how to establish a reliable interfacial interaction is the key requirement for the successful integration of geometrically different components. Here, we present 1D/2D heterodimensional hybrids via dopant induced hybridization of 2D Ti3C2T x MXene with 1D nitrogen-doped graphene nanoribbon. Edge abundant nanoribbon structures allow a high level nitrogen doping (∼6.8 at%), desirable for the strong coordination interaction with Ti3C2T x MXene surface. For piezoresistive pressure sensor application, strong adhesion between the conductive layers and at the conductive layer/elastomer interface significantly diminishes the sensing hysteresis down to 1.33% and enhances the sensing stability up to 10 000 cycles at high pressure (100 kPa). Moreover, large-area pressure sensor array reveals a high potential for smart seat cushion-based posture monitoring application with high accuracy (>95%) by exploiting machine learning algorithm.

An effective pathway to build macroscopic scale functional architectures bearing diverse structural dimensions is one of the critical challenges in the two-dimensional (2D) MXene research area. Unfortunately, assembling MXene without adhesive binder is largely limited due to its innate brittle nature and the relatively weak inter-flake van der Waals contact, in contrast to other mechanically compliant 2D materials such as graphene. Herein, an electrochemical selfassembly of pure Ti 3 C 2 T x MXenes is presented for functional multidimensional MXene structures, effectively driven by layerby-layer spontaneous interfacial reduction at metal template surfaces and subsequent defunctionalization. A three-dimensional open porous aerogel as well as 2D highly stacked thin film structures could be readily obtained in this approach, along with largely enhanced electrical properties induced by spontaneous removal of charge-trapping oxygen functional groups. Accordingly, supercapacitors and electromagnetic interference shielding films based on the multidimensional assembly demonstrate excellent performances.

In anion exchange membrane fuel cells (AEMFCs) for green energy, silver (Ag)-based compounds are promising non-Pt electrocatalysts with high catalytic activity and a low cost for the oxygen reduction reaction (ORR). Although silver chloride (AgCl) shows high catalytic activity due to the ligand effect originating from the electronegativity difference between the two elements, its low electroconductivity remains a significant issue. Here, we report Ag-AgCl core–shell nanowires decorated with AgCl (AgCl-Ag@AgCl NWs) that have a structure capable of simultaneously exhibiting the good conductivity of a long silver (Ag) core and the high ORR catalytic activity of silver chloride (AgCl). In addition, by decorating AgCl nanoclusters on the AgCl shell, AgCl-Ag@AgCl NWs have an enlarged active surface. As a result, AgCl-Ag@AgCl NWs show highly improved catalytic performance (half-wave potential = 0.78 V vs a reversible hydrogen electrode (RHE), limiting current density = 4.51 mA/cm2). Accelerated durability tests (ADTs) confirm the high stability of AgCl-Ag@AgCl NWs after 4000 cycles of potential sweep and rotating ring disk electrode (RRDE) analysis shows remarkable efficiency with the high electron transfer number (n) (3.97). We also use density functional theory (DFT) calculation to confirm charge transfer, which improves the activity of our catalysts.

Valence change-type resistance switching behaviors in oxides can be understood by well-established physical models describing the field-driven oxygen vacancy distribution change. In those models, electroformed residual oxygen vacancy filaments are crucial as they work as an electric field concentrator and limit the oxygen vacancy movement along the vertical direction. Therefore, their movement outward by diffusion is negligible. However, this situation may not be applicable in the electroforming-free system, where the field-driven movement is less prominent, and the isotropic oxygen vacancy diffusion by concentration gradient is more significant, which has not been given much consideration in the conventional model. Here, we propose a modified physical model that considers the change in the oxygen vacancies’ charged state depending on their concentrations and the resulting change in diffusivity during switching to interpret the electroforming-free device behaviors. The model suggests formation of an hourglass-shaped filament constituting a lower concentration of oxygen vacancies due to the fluid oxygen diffusion in the thin oxide. Consequently, the proposed model can explain the electroforming-free device behaviors, including the retention failure mechanism, and suggest an optimized filament configuration for improved retention characteristics. The proposed model can plausibly explain both the electroformed and the electroforming-free devices. Therefore, it can be a standard model for valence change memristors.

Suspended nanostructures play an important role in enhancing the performance of a diverse group of nanodevices. However, realizing a good arrangement and suspension for nanostructures of various shapes remains a...

Two-dimensional (2D) materials are promising components for defect passivation of metal halide perovskites. Unfortunately, commonly used polydisperse liquid-exfoliated 2D materials generally suffer from heterogeneous structures and properties while incorporated into perovskite films. We introduce monodisperse multifunctional 2D crystalline carbon nitride, poly­(triazine imide) (PTI), as an effective defect passivation agent in perovskite films via typical solution processing. Incorporation of PTI into perovskite film can be readily attained by simple solution mixing of PTI dispersions with perovskite precursor solutions, resulting in the highly selective distribution of PTI localized at the defective crystal grain boundaries and layer interfaces in the functional perovskite layer. Several chemical, optical, and electronic characterizations, in conjunction with density functional theory calculations, reveal multiple beneficial roles from PTI: passivation of undercoordinated organic cations at the surface of perovskite crystal, suppression of ion migration by blocking diffusion channels, and prevention of hole quenching at perovskite/SnO2 interfaces. Consequently, a noticeably improved power conversion efficiency is achieved in perovskite solar cells, accompanied with promoted stability under humid air and thermal stress. Our strategy highlights the potential of judiciously designed 2D materials as a simple-to-implement material for various optoelectronic devices, including solar cells, based on hybrid perovskites.

The alkaline environment in anion-exchange membrane fuel cells allows the use of Pt-free electrocatalysts, thus reducing the system cost. We performed a theoretical high-throughput study of various low-cost Ag-based oxygen reduction reaction anode electrocatalysts and assessed their catalytic performance using density functional theory. From the Materials Project database, a total of 106 binary Ag alloys were investigated by estimating their heat of formation, dissolution potential, and overpotential on low-index surfaces. We confirmed that EuAg5, BaAg5, and SrAg5 have higher catalytic activities and durabilities than pure Ag. By following the chemical trend of the results, we further proposed LaAg5 and PrAg5, which were not included in the database, as promising candidates. All candidates are in the space group P6/mmm and contain alkaline earth metal or lanthanide elements.