Metal-like Electrical Conductivity Research Articles

Nitrogen-Doped Graphene-Like Carbon Intercalated MXene Heterostructure Electrodes for Enhanced Sodium- and Lithium-Ion Storage.

MXene is investigated as an electrode material for different energy storage systems due to layered structures and metal-like electrical conductivity. Experimental results show MXenes possess excellent cycling performance as anode materials, especially at large current densities. However, the reversible capacity is relatively low, which is a significant barrier to meeting the demands of industrial applications. This work synthesizes N-doped graphene-like carbon (NGC) intercalated Ti3C2Tx (NGC-Ti3C2Tx) van der Waals heterostructure by an in situ method. The as-prepared NGC-Ti3C2Tx van der Waals heterostructure is employed as sodium-ion and lithium-ion battery electrodes. For sodium-ion batteries, a reversible specific capacity of 305mAhg-1 is achieved at a specific current of 20mAg-1, 2.3 times higher than that of Ti3C2Tx. For lithium-ion batteries, a reversible capacity of 400mAhg-1 at a specific current of 20mAg-1 is 1.5 times higher than that of Ti3C2Tx. Both sodium-ion and lithium-ion batteries made from NGC-Ti3C2Tx shows high cycling stability. The theoretical calculations also verify the remarkable improvement in battery capacity within the NGC-Ti3C2O2 system, attributed to the additional adsorption of working ions at the edge states of NGC. This work offers an innovative way to synthesize a new van der Waals heterostructure and provides a new route to improve the electrochemical performance significantly.

Anderson Localization of Phonons in Thermally Superinsulating Graphene Aerogels with Metal-Like Electrical Conductivity.

In the quest to improve energy efficiency and design better thermal insulators, various engineering strategies have been extensively investigated to minimize heat transfer through a material. Yet, the suppression of thermal transport in a material remains elusive because heat can be transferred by multiple energy carriers. Here, the realization of Anderson localization of phonons in a random 3D elastic network of graphene is reported. It is shown that thermal conductivity in a cellular graphene aerogel can be drastically reduced to 0.9mWm-1K-1 by the application of compressive strain while keeping a high metal-like electrical conductivity of 120Sm-1 and ampacity of 0.9A. The experiments reveal that the strain can cause phonon localization over a broad compression range. The remaining heat flow in the material is dominated by charge transport. Conversely, electrical conductivity exhibits a gradual increase with increasing compressive strain, opposite to the thermal conductivity. These results imply that strain engineering provides the ability to independently tune charge and heat transport, establishing a new paradigm for controlling phonon and charge conduction in solids. This approach will enable the development of a new type of high-performance insulation solutions and thermally superinsulating materials with metal-like electrical conductivity.

Highly sensitive and reversible MXene-based micro quartz tuning fork gas sensors with tunable selectivity

Due to their distinctive morphology, significant surface-to-volume ratio, and metal-like electrical conductivity, MXenes have emerged as highly promising gas-sensing materials. Traditional MXene-based gas sensors predominantly rely on the electrical conductivity of MXenes for signal transduction. However, it is crucial to explore alternative signal transduction mechanisms to fully unlock the potential of MXenes in gas sensing applications. In this study, we have successfully showcased the development of a mass-transduction-based MXene gas sensor, utilizing MXenes as the adaptable receptor and MQTF as the transducer. The interaction between the gas analyte and MXenes induces a change in mass, resulting in a resonant frequency shift of the MQTF. This signal transduction mechanism eliminates the dependency on the electrical conductivity of MXenes, offering a broader range of possibilities for chemical modification of MXenes without concerns about compromising their conductivity. By engineering Ti3C2Tx surfaces, we have demonstrated high sensitivity and selectivity tuning of MXene-MQTF gas sensors for detecting CO, SO2, and NH3. This antisymmetric mass-transduction-based (low-cost, stable, sensitive, and practical tuning fork-based) MXene gas sensor demonstrated exceptional sensing performance, customizable selectivity, and high cost-effectiveness. This study paves the way for designing high-performance MXene-based chemical sensors and expands the scope of potential applications in air quality monitoring, wearable devices, the Internet of Things (IoT), and robotics.

A Breathable Fibrous Membrane with Coaxially Heterogeneous Conductive Networks toward Personal Thermal Management and Electromagnetic Interference Shielding.

The expeditious growth of wearable electronic devices has boomed the development of versatile smart textiles for personal health-related applications. In practice, integrated high-performance systems still face challenges of compromised breathability, high cost, and complicated manufacturing processes. Herein, a breathable fibrous membrane with dual-driven heating and electromagnetic interference (EMI) shielding performance is developed through a facile process of electrospinning followed by targeted conformal deposition. The approach constructs a robust hierarchically coaxial heterostructure consisting of elastic polymers as supportive "core" and dual-conductive components of polypyrrole and copper sulfide (CuS) nanosheets as continuous "sheath" at the fiber level. The CuS nanosheets with metal-like electrical conductivity demonstrate the promising potential to substitute the expensive conductive nano-materials with a complex fabricating process. The as-prepared fibrous membrane exhibits high electrical conductivity (70.38 S cm-1 ), exceptional active heating effects, including solar heating (saturation temperature of 69.7 °C at 1 sun) and Joule heating (75.2 °C at 2.9V), and impressive EMI shielding performance (50.11dB in the X-band), coupled with favorable air permeability (161.4mm s-1 at 200Pa) and efficient water vapor transmittance (118.9g m-2 h). This work opens up a new avenue to fabricate versatile wearable devices for personal thermal management and health protection.

Coexistence of Superhardness and Metal-Like Electrical Conductivity in High-Entropy Dodecaboride Composite with Atomic-Scale Interlocks.

High electrical conductivity and super high hardness are two sought-after material properties, but both are contradictory because the effective suppression of dislocation movement generally increases the scattering of conducting electrons. Here we synthesized a high-entropy dodecaboride composite (HEDC) with a large number of atomic-scale interlocking layers. It shows a Vickers hardness of 51.2 ± 3.6 GPa under an applied load of 0.49 N and an electrical resistivity of 44.5 μΩ·cm at room temperature. Such HEDC achieves superhardness by inheriting the high intrinsic hardness of its constituent phases and restricting the dislocation motion to further enhance the extrinsic hardness through forming numerous atom-scale interlocks between different slip systems. Moreover, the HEDC maintains the excellent electrical conductivity of the constituent borides, and the competition between two correlating structures produces the special kind of coherent boundary that minimizes the scattering of conducting electrons and does not largely deteriorate the electrical conductivity.

Bimetallic nickel iron sulfide directly grown on defect-rich Ti3C2 MXene as an efficient bifunctional electrocatalyst for water electrolysis

Water electrolysis has been regarded as ideal method for producing high-purity hydrogen without the generation of environmental pollutants. Accordingly, the development of precious metal-free electrocatalysts that demonstrate high activity for both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) is essential for practical water electrolysis. Herein, porosity-engineered Ti3C2 MXene is employed as an efficient substrate for a bimetallic Ni-Fe-S electrocatalyst. The porous and defect-rich Ti3C2 (D-Ti3C2) flakes provide metal-like electrical conductivity and large surface area for direct growth of active species. Simultaneously, the Ni-Fe-S nanoparticles, constructed through a strong coupling between NiS2 and (Ni,Fe)S2 solid solution, not only serve as active sites with rich redox properties, but also generate charge transfer channels for electrochemical reactions. Leveraging these advantageous properties, the resulting Ni-Fe-S/D-Ti3C2 electrocatalyst exhibits excellent bifunctional electrocatalytic performance toward both OER and HER. As a result, the symmetric water electrolysis cell using the Ni-Fe-S/D-Ti3C2 requires a low cell voltage of 1.621 V to deliver current density of 10 mA cm−2, and shows stable electrocatalytic performance over 100 h of continuous operation.

A cerebral cortex-like structured metallized elastomer for high-performance triboelectric nanogenerator

The advancement of wearable electronics, particularly triboelectric nanogenerators (TENGs), relies on the development of flexible, stretchable, and compressible electrodes that possess a large active surface area, high electrical conductivity, and excellent mechanical stability and deformability. However, existing elastomeric electrodes face challenges in meeting all of these requirements. Herein, we present a novel approach to address these limitations and create electrodes with elastomeric properties, stable metal-like electrical conductivity, and an expanded active surface area. For this goal, we perform an assembly of metal nanoparticles (NPs) in toluene and amine-functionalized organic linkers in alcohol onto the thiol-functionalized, embossed-structured elastomer. Particularly, the assembly process involves ligand exchange reaction-mediated metal NPs and subjecting them to solvent-swelling/deswelling of the embossed PDMS. This process induces the formation of cerebral cortex-like structured elastomer electrode, which is subsequently electroplated with Ni. The resulting electrodes exhibit metal-like electrical conductivity, elastomer-like flexibility, and cerebral cortex-like structure with substantially large surface area and high stress relieving properties. When combined with an intaglio-structured dielectric PDMS electrode, the device exhibits impressive TENG performance, surpassing the performance of conventional TENGs. This approach provides a basis for developing and designing a variety of high-performance flexible electronics, including TENGs.

XMoSiN2 (X = S, Se, Te): A novel 2D Janus semiconductor with ultra-high carrier mobility and excellent thermoelectric performance

Two-dimensional (2D) semiconductor is a potential candidate for thermoelectric materials due to its high Seebeck coefficient. However, its high lattice thermal conductivity limits its applications in the field of thermoelectric materials. Here, we constructed an unsymmetrical 2D Janus semiconductor XMoSiN2(X = S, Se, Te) based on to significantly reduce the lattice thermal conductivity to only one-sixth that of at 300 K. We found that XMoSiN2 had an ultra-high carrier mobility up to 4640 cm2V−1s−1 leading to a metal-like electrical conductivity. Meanwhile, XMoSiN2 reserved the high Seebeck coefficient of . The lower lattice thermal conductivity and metal-like electrical conductivity resulted in excellent thermoelectric performance. possessed a record-high ZT value of 3.57 at 900 K. We believed that other materials with a similar structure to XMoSiN2 can also be potential candidates for high-performance thermoelectric materials. Our work provides valuable insights into designing novel high-performance thermoelectric materials.

High Thermoelectric Performance of a Novel γ-PbSnX2 (X = S, Se, Te) Monolayer: Predicted Using First Principles.

Two-dimensional (2D) group IV metal chalcogenides are potential candidates for thermoelectric (TE) applications due to their unique structural properties. In this paper, we predicted a 2D monolayer group IV metal chalcogenide semiconductor γ-PbSn2 (X = S, Se, Te), and first-principles calculations and Boltzmann transport theory were used to study the thermoelectric performance. We found that γ-PbSnX2 had an ultra-high carrier mobility of up to 4.04 × 103 cm2 V-1 s-1, which produced metal-like electrical conductivity. Moreover, γ-PbSn2 not only has a very high Seebeck coefficient, which leads to a high power factor, but also shows an intrinsically low lattice thermal conductivity of 6-8 W/mK at room temperature. The lower lattice thermal conductivity and high power factors resulted in excellent thermoelectric performance. The ZT values of γ-PbSnS2 and γ-PbSnSe2 were as high as 2.65 and 2.96 at 900 K, respectively. The result suggests that the γ-PbSnX2 monolayer is a better candidates for excellent thermoelectric performance.

Recent advances of flexible MXene physical sensor to wearable electronics

MXenes, as a family of two-dimensional (2D) lamellar material of transition metal carbides, nitrides and carbon/nitrides, is an ideal choice for flexible sensing materials because of its metal-like electrical conductivity, adjustable layer spacing, good hydrophilicity and mechanical properties. Flexible wearable sensors based on various electromechanical properties and structural forms of MXene have also emerged in recent years, such as MXene fiber-based fabrics, flexible membrane structures, and three-dimensional aerogel/hydrogel gel structures. All these structural sensors have shown different advantages and sensing effects, and some corresponding issues are also brought out. Therefore, the improvement of comprehensive performance for MXene based flexible sensors have always been a concern. In this review, the structure, fundamental properties, synthetic routes of MXene are briefly summarized. Additionally, the fabrication of flexible sensing materials with different configuration, and state-of-the-art progress of MXene based wearable physical sensors (including pressure, strain, humidity and temperature sensor) are highlighted. At last, the current challenges and their future research directions toward advancing wearable MXene sensors are presented and discussed.

Effect of mechanical ball milling on the electrical and powder bed properties of gas-atomized Ti–48Al–2Cr–2Nb and elucidation of the smoke mechanism in the powder bed fusion electron beam melting process

Smoke is unexpected powder-splashing caused by electrostatic force and is one of the main problems hindering the process stability and applicability of the powder bed fusion electron beam (PBF-EB) technology. In this study, mechanical stimulation was suggested to suppress smoke of gas-atomized (GA) Ti–48Al–2Cr–2Nb powder using Al2O3 and WC ball milling. The deformation mechanism of the GA powder depending on the ball milling media was discussed based on the developed particle morphology distribution map and contact mechanics simulation. It was revealed that the rapid decrement of flowability and packing density after WC ball milling owing to the formation of angular fragments by the brittle fracture. The variation of surface and electrical properties by mechanical stimulation was investigated via XPS, TEM, Impedance analysis. The electrical resistivity of the ball-milled powders gradually decreased with increasing milling duration, despite the increased oxide film thickness, and the capacitive response disappeared in Al-60 and WC-30 via metal–insulator transition. This could be due to the accumulation of strain and defects on the oxide film via mechanical stimulation. The smoke mechanism of ball-milled powders was discussed based on the percolation theory. In the smoke experiment, smoke was more suppressed for WC-10 and WC-20 than that for Al-40 and Al-50, respectively, despite the longer charge dissipation time. This could be due to the high probability of contact with conductive particles. For the Al-60 and WC-30 powders, smoke was further restricted by the formation of a percolation cluster with metal-like electrical conductivity. We believe that this study will contribute to a better understanding of the smoke mechanism and process optimization of the PBF-EB.

MXene-based flexible sensors: A review

MXenes are an emerging family of two-dimensional (2D) materials which exhibits unique characteristics such as metal-like thermal and electrical conductivity, huge surface area, biocompatibility, low toxicity, excellent electrochemical performance, remarkable chemical stability, antibacterial activity, and hydrophilicity. Initially, MXene materials were synthesized by selectively etching metal layers from MAX phases, layered transition metal carbides, and carbonitrides with hydrofluoric acid. Multiple novel synthesis methods have since been developed for the creation of MXenes with improved surface chemistries using non-aqueous etchants, molten salts, fluoride salts, and various acid halogens. Due to the promising potential of MXenes, they have emerged as attractive 2D materials with applications in various fields such as energy storage, sensing, and biomedical. This review provides a comprehensive overview of MXenes and discusses the synthesis and properties of MXenes, including the methods of etching, delamination, and modification/functionalization, as well as the electrical properties of MXenes. Following this, the recent advances in the development of various MXene-based sensors are presented. Finally, the challenges and opportunities for future research on the development of MXenes-based sensors are discussed.

Fibril-Type Textile Electrodes Enabling Extremely High Areal Capacity through Pseudocapacitive Electroplating onto Chalcogenide Nanoparticle-Encapsulated Fibrils.

Effective incorporation of conductive and energy storage materials into 3D porous textiles plays a pivotal role in developing and designing high-performance energy storage devices. Here, a fibril-type textile pseudocapacitor electrode with outstanding capacity, good rate capability, and excellent mechanical stability through controlled interfacial interaction-induced electroplating is reported. First, tetraoctylammonium bromide-stabilizedcopper sulfidenanoparticles (TOABr-CuS NPs) are uniformly assembled onto cotton textiles. This approach converts insulating textiles to conductive textiles preserving their intrinsically porous structure with an extremely large surface area. For the preparation of textile current collector with bulk metal-like electrical conductivity, Ni is additionally electroplated onto the CuS NP-assembled textiles (i.e., Ni-EPT). Furthermore, a pseudocapacitive NiCo-layered double hydroxide (LDH) layer is subsequently electroplated onto Ni-EPT for the cathode. The formed NiCo-LDH electroplated textiles (i.e., NiCo-EPT) exhibit a high areal capacitance of 12.2 F cm-2 (at 10mA cm-2 ), good rate performance, and excellent cycling stability. Particularly, the areal capacity of NiCo-EPT can be further increased through their subsequent stacking. The 3-stack NiCo-EPT delivers an unprecedentedly high areal capacitance of 28.8 F cm-2 (at 30mA cm-2 ), which outperforms those of textile-based pseudocapacitor electrodes reported to date.

Tough and Fatigue Resistant Cellulose Nanocrystal Stitched Ti3 C2 Tx MXene Films.

Ti3 C2 Tx MXene (or "MXene" for simplicity) has gained noteworthy attention for its metal-like electrical conductivity and high electrochemical capacitance-a unique blend of properties attractive toward a wide range of applications such as energy storage, healthcare monitoring, and electromagnetic interference shielding. However, processing MXene architectures using conventional methods often deals with the presence of defects, voids, and isotropic flake arrangements, resulting in a trade-off in properties. Here, a sequential bridging (SB) strategy is reported to fabricate dense, freestanding MXene films of interconnected flakes with minimal defects, significantly enhancing its mechanical properties, specifically tensile strength (≈285MPa) and breaking energy (≈16.1MJm-3 ), while retaining substantial values of electrical conductivity (≈3050Scm-1 ) and electrochemical capacitance (≈920Fcm-3 ). This SB method first involves forming a cellulose nanocrystal-stitched MXene framework, followed by infiltration with structure-densifying calcium cations (Ca2+ ), resulting in tough and fatigue resistant films with anisotropic, evenly spaced, and strongly interconnected flakes - properties essential for developing high-performance energy-storage devices. It is anticipated that the knowledge gained in this work will be extended toward improving the robustness and retaining the electronic properties of 2D nanomaterial-based macroarchitectures.

Ten Years of Progress in the Synthesis and Development of MXenes.

Since their discovery in 2011, the number of 2D transition metal carbides and nitrides (MXenes) has steadily increased. Currently more than 40 MXene compositions exist. The ultimate number is far greater and in time they may develop into the largest family of 2D materials known. MXenes' unique properties, such as their metal-like electrical conductivity reaching ≈20000 S cm-1 , render them quite useful in a large number of applications, including energy storage, optoelectronic, biomedical, communications, and environmental. The number of MXene papers and patents published has been growing quickly. The first MXene generation is synthesized using selective etching of metal layers from the MAX phases, layered transition metal carbides and carbonitrides using hydrofluoric acid. Since then, multiple synthesis approaches have been developed, including selective etching in a mixture of fluoride salts and various acids, non-aqueous etchants, halogens, and molten salts, allowing for the synthesis of new MXenes with better control over their surface chemistries. Herein, a brief historical overview of the first 10 years of MXene research and a perspective on their synthesis and future development are provided. The fact that their production is readily scalable in aqueous environments, with high yields bodes well for their commercialization.

Sensing with MXenes: Progress and Prospects.

Various fields of study consider MXene a revolutionary 2D material. Particularly in the field of sensors, the metal-like high electrical conductivity and large surface area of MXenes are desirable characteristics as an alternative sensor material that can transcend the boundaries of existing sensor technology. This critical review provides a comprehensive overview of recent advances in MXene-based sensor technology and a roadmap for commercializing MXene-based sensors. The existing sensors are systematically categorized as chemical, biological, and physical sensors. Each category is then classified into various subcategories depending on the electrical, electrochemical, structural, or optical sensing mechanism, which are the four fundamental working mechanisms of sensors. Representative structural and electrical approaches for boosting the performance of each category are presented. Finally, factors that hinder commercializing MXene-based sensors are discussed, and several breakthroughs in realizing commercially available MXene-based sensors are suggested. This review provides broad insights pertaining to previous and existing MXene-based sensor technology and perspectives on the future generation of low-cost, high-performance, and multimodal sensors for soft-electronics applications.

Superposition of semiconductor and semi-metal properties of self-assembled 2D SnTiS3 heterostructures

Two-dimensional metal dichalcogenide/monochalcogenide thin flakes have attracted much attention owing to their remarkable electronic and electrochemical properties; however, chemical instability limits their applications. Chemical vapor transport (CVT)-synthesized SnTiS3 thin flakes exhibit misfit heterojunction structure and are highly stable in ambient conditions, offering a great opportunity to exploit the properties of two distinct constituent materials: semiconductor SnS and semi-metal TiS2. We demonstrated that in addition to a metal-like electrical conductivity of 921 S/cm, the SnTiS3 thin flakes exhibit a strong bandgap emission at 1.9 eV, owing to the weak van der Waals interaction within the misfit-layer stackings. Our work shows that the misfit heterojunction structure preserves the electronic properties and lattice vibrations of the individual constituent monolayers and thus holds the promise to bridge the bandgap and carrier mobility discrepancy between graphene and recently established 2D transition metal dichalcogenide materials. Moreover, we also present a way to identify the top layer of SnTiS3 misfit compound layers and their related work function, which is essential for deployment of van der Waals misfit layers in future optoelectronic devices.

Towards excellent electrical conductivity and high-rate capability: A degenerate superlattice Ni3(S)1.1(S2)0.9 micropyramids electrode

Degenerate semiconductor is very highly desired in energy conversion and storage technologies due to its metal-like conduction behaviors. This is the first time the doping S2 in Ni3S2 lattice into chemically homogeneous Ni3(S)1.1(S2)0.9 superlattice structure is proposed to induce a degenerate characteristic towards excellent electrical conductivity and high-rate capability. In this study, a series of the chemically homogeneous S2-doped Ni3(S)1.8(S2)0.2, Ni3(S)1.6(S2)0.4, Ni3(S)1.3(S2)0.7, and Ni3(S)1.1(S2)0.9 micropyramid arrays on Ni foam were synthesized by reacting the Ni foam and alkaline sulfur aqueous solution in different S22- concentrations. The perfect Ni3(S)1.1(S2)0.9 superlattice structure corresponds to the periodic S–Ni–S2 atom arrangements in whole crystal lattice, which endows a degenerate characteristic of metal-like electrical conductivity to significantly improve the electrochemical performance. The bulk series resistance (Rs) value is only 0.62 Ω, while the charge-transfer resistance (Rct) is nearly 0 Ω in the superlattice Ni3(S)1.1(S2)0.9 electrode. As a cathode material for application in lithium ion batteries (LIBs), a very high specific capacity of 874 mAh g−1 is achieved at current density of 200 mA g−1. Remarkably, it still holds a high capacity of 565 mAh g−1 at current density of 500 mA g−1, indicating its superior high-rate capability. This study reveals that the periodic S–Ni–S2 atom arrangements in crystal lattice is a key factor in determining the superlattice structure, high specific capacity, and the dynamic behaviors of electron/ion transport.

Understanding the Structure and Properties of Sesqui‐Chalcogenides (i.e., V2VI3 or Pn2Ch3 (Pn = Pnictogen, Ch = Chalcogen) Compounds) from a Bonding Perspective

A number of sesqui-chalcogenides show remarkable properties, which make them attractive for applications as thermoelectrics, topological insulators, and phase-change materials. To see if these properties can be related to a special bonding mechanism, seven sesqui-chalcogenides (Bi2 Te3 , Bi2 Se3 , Bi2 S3 , Sb2 Te3 , Sb2 Se3 , Sb2 S3 , and β-As2 Te3 ) and GaSe are investigated. Atom probe tomography studies reveal that four of the seven sesqui-chalcogenides (Bi2 Te3 , Bi2 Se3 , Sb2 Te3 , and β-As2 Te3 ) show an unconventional bond-breaking mechanism. The same four compounds evidence a remarkable property portfolio in density functional theory calculations including large Born effective charges, high optical dielectric constants, low Debye temperatures and an almost metal-like electrical conductivity. These results are indicative for unconventional bonding leading to physical properties distinctively different from those caused by covalent, metallic, or ionic bonding. The experiments reveal that this bonding mechanism prevails in four sesqui-chalcogenides, characterized by rather short interlayer distances at the van der Waals like gaps, suggestive of significant interlayer coupling. These conclusions are further supported by a subsequent quantum-chemistry-based bonding analysis employing charge partitioning, which reveals that the four sesqui-chalcogenides with unconventional properties are characterized by modest levels of charge transfer and sharing of about one electron between adjacent atoms. Finally, the 3D maps for different properties reveal discernible property trends and enable material design.

Multifunctional Nanocomposites with High Strength and Capacitance Using 2D MXene and 1D Nanocellulose.

The family of two-dimensional (2D) metal carbides and nitrides, known as MXenes, are among the most promising electrode materials for supercapacitors thanks to their high metal-like electrical conductivity and surface-functional-group-enabled pseudocapacitance. A major drawback of these materials is, however, the low mechanical strength, which prevents their applications in lightweight, flexible electronics. A strategy of assembling freestanding and mechanically robust MXene (Ti3 C2 Tx ) nanocomposites with one-dimensional (1D) cellulose nanofibrils (CNFs) from their stable colloidal dispersions is reported. The high aspect ratio of CNF (width of ≈3.5 nm and length reaching tens of micrometers) and their special interactions with MXene enable nanocomposites with high mechanical strength without sacrificing electrochemical performance. CNF loading up to 20%, for example, shows a remarkably high mechanical strength of 341 MPa (an order of magnitude higher than pristine MXene films of 29 MPa) while still maintaining a high capacitance of 298 F g-1 and a high conductivity of 295 S cm-1 . It is also demonstrated that MXene/CNF hybrid dispersions can be used as inks to print flexible micro-supercapacitors with precise dimensions. This work paves the way for fabrication of robust multifunctional MXene nanocomposites for printed and lightweight structural devices.