Interlayer Entropy Engineering Inducing the Symmetry-Broken Layered Oxide Cathodes to Activate Reversible High-Voltage Redox Reaction.

The as-reported doping entropy engineering of electrode materials that are usually realized by the sharing of multiple metal elements with the metal element from the lattice body, potentially has three shortages of stringent synthesis conditions, large active element loss, and serious lattice distortion. Herein, an interlayer entropy engineering of layered oxide cathodes is proposed, where the multiple metal ions are simultaneously intercalated into the same interlayer sites, thus avoiding the three shortages. Concretely, a novel interlayer medium-entropy V2O5 ((MnCoNiMgZn)0.26V2O5∙0.84H2O) is successfully constructed by a one-step hydrothermal method. The interlayer medium-entropy effect is revealed to be that five metal ions pre-intercalation induces the local symmetry-broken [VO6] octahedra in bilayer V2O5, thus activating the reversible high-voltage redox reaction, inhibiting the layer slip and following phase transformation by its pinning effect, and enhancing the charge transfer kinetics. As a result, the medium-entropy cathode realizes the trade-off between specific capacity and structural stability with a discharge capacity of 152 mAh g-1 at 0.1 A g-1 after 100 cycles, and a capacity retention rate of 98.7% at 0.5 A g-1 after 150 cycles for Li+ storage. This engineering provides a new guideline for the rational design of high-performance layered oxide cathodes.

Enabling Quasi-Zero-Strain Behavior of Layered Oxide Cathodes via Multiple-cations Induced Order-to-Disorder Transition.

The chemically pre-intercalated lattice engineering is widely applied to elevate the electronic conductivity, expand the interlayer spacing, and improve the structural stability of layered oxide cathodes. However, the mainstream unitary metal ion pre-intercalation generally produces the cation/vacancy ordered superstructure, which astricts the further improvement of lattice respiration and charge-carrier ion storage and diffusion. Herein, a multiple metal ions pre-intercalation lattice engineering is proposed to break the cation/vacancy ordered superstructure. Taking the bilayer V2O5 as an example, Ni, Co, and Zn ternary ions are simultaneously pre-intercalated into its interlayer space (NiCoZnVO). It is revealed that the Ni─Co neighboring characteristic caused by Ni(3d)-O(2p)-Co(3d) orbital coupling and the Co-Zn/Ni-Zn repulsion effect due to chemical bond incompatibility, endow the NiCoZnVO sample with the cation/vacancy disordered structure. This not only reduces the Li+ diffusion barrier, but also increases the diffusion dimension of Li+ (from one-dimension to two-dimension). Particularly, Ni, Co, and Zn ions co-pre-intercalation causes a prestress, which realizes a quasi-zero-strain structure at high-voltage window upon charging/discharging process. The functions of Ni ion stabilizing the lattice structure and Co or Zn ions activating more Li+ reversible storage reaction of V5+/V4+ are further revealed. The cation/vacancy disordered structure significantly enhances Li+ storage properties of NiCoZnVO cathode.

Tuning Redox Behavior of Sulfur Cathodes Via Ternary-Coordinated Single Fe Atom in Lithium-Sulfur Batteries.

Modulating the coordination configuration of single Fe atom has been an efficient strategy to strengthen the redox dynamics for lithium-sulfur batteries (LSBs) but remains challenging. Herein, the single Fe atom is functioned with nitrogen and carbon atoms in the first shell, and simultaneously, oxidized sulfur (─SOx) in the second shell, which presents a lower antibonding state and well address the redox activity of sulfur cathodes. In the ternary-coordinated single Fe atom catalyst (FeN2C2-SOx-NC), the binary structure of FeN2C2 provides a lower Fe-S bonding strength and d-p orbital hybridization, which obviously optimizes the adsorption and desorption behavior of sulfur species during the reduction and oxidation reaction processes. Simultaneously, the ─SOx redistributes the electron density of the coordinating nitrogen atoms, which possesses high electron-withdrawing ability and develops electrocatalytic activity. As a result, the sulfur cathodes with FeN2C2-SOx-NC present an excellent high-rate cyclic performance, accompanied by a capacity decay rate of 0.08% per cycle for 500 cycles at 4.0 C. This study provides new insights for optimizing the redox dynamics of sulfur cathodes in LSBs at the atomic level.

Crystal phase engineering of nanoflower-like hollow MoSe2boosting polysulfide conversion for lithium-sulfur batteries.

The battery performance of sulfur cathode has obviously depended on the redox reaction kinetics of polysulfides upon cycling. Herein, an effective strategy was proposed to achieve the conversion from 2H (semiconductor phase) to 1T (metal phase) in hollow nano-flowered molybdenum selenide sphere (HFSMS) through crystal phase engineering. The HFSMS with different phase ratio was realized by regulating the proportion of reducing agents. Specifically, the 1T phase content can reach up to 60.8%, and then subsequently decreased to 59.1% with the further increase of the reducing agent. The as-prepared HFSMS with the 1T phase content of 60.8% showed a smallest Tafel slopes (49.99 and 79.65 mV/dec in reduction and oxidation process, respectively), fastest response time and highest response current (520 s, 0.459 mA in Li2S deposition test), which further exhibited excellent catalytic activity and faster reaction kinetics. This result was verified by electrochemical performance, which manifested as stable cycle life with only 0.112% capacity decay per cycle. It was found that the hollow structure can ensures a rich sulfur storage space, and effectually buffer the volume changes of the active substance. More importantly, the improved performance is attributed to the introduction of the 1T phase, which significantly improves the catalytic activity of MoSe2with promoting the polysulfide conversion.

Fabrication of a flexible porous polypyrrole film with a 3D micro-nanostructure and its electrochemical properties.

Flexible energy storage systems have become attractive alternatives for applications in wearable energy storage and sensor devices. This study reports a simple electro-polymerization method for the fabrication of PPy films coated on PPy nanotubes (PPy NTs), which are binding-free, self-standing, and could be used as a flexible electrode for supercapacitors. With optimized kinetics for ion transportation, the mass specific capacitance of the flexible porous PPy films can be elevated to 1.36 F cm-2 at a charging/discharging rate of 2 mA cm-2 (0.45 A g-1). The mass specific capacitance of the flexible porous PPy films reaches 6.5 times as large as that of compact PPy films at a scan rate of 20 mV s-1. Furthermore, due to the large free space for volume change, the capacitance fading of the flexible porous PPy films is less than 3% after 10 000 cycles. This novel design provides an efficient method to synthesize high-performance, flexible and low-cost materials used in supercapacitors.

Additive Manufacturing of Two-Dimensional Conductive Metal-Organic Framework with Multidimensional Hybrid Architectures for High-Performance Energy Storage.

Two-dimensional conductive metal-organic frameworks (2D CMOFs) can be regarded as high-performance electrode substances owing to their rich hierarchical porous architecture and excellent electrical conductivity. However, the sluggish kinetics behavior of electrodes within the bulk structure restricts their advances in energy storage fields. Herein, a series of graphene-based mixed-dimensional composite aerogels are achieved by incorporating the 2D M-tetrahydroxy-1,4-quinone (M-THQ) (M = Cu, Cu/Co, or Cu/Ni) into CNTs@rGO aerogel electrodes using a 3D-printing direct ink writing (DIW) technique. Benefiting from the high capacity of M-THQ and abundant porosity of the 3D-printed microlattice electrodes, an excellent capacitive performance of the M-THQ@CNTs@rGO cathodes is achieved based on the fast electron/ion transport. Furthermore, the 3D-printed lithium-ion hybrid supercapacitor (LIHCs) device assembled with Cu/Co-THQ@CNTs@rGO cathode and C60@VNNWs@rGO anode delivers a remarkable electrochemical performance. More importantly, this work manifests the practicability of printing 2D CMOFs electrodes, which provides a substantial research basis for 3D printing energy storage.

Engineering p-Band Center of Oxygen Boosting H+ Intercalation in δ-MnO2 for Aqueous Zinc Ion Batteries.

In aqueous zinc ion batteries (ZIBs), the H+ intercalation possesses superior electrochemical kinetics with excellent rate capability, however, precisely modulating H+ intercalation has been still challenging. Herein, a critical modification of pre-intercalating metal ions in the MnO2 interlayer (M-MnO2 ) with controllable p-band center (ϵp ) of O is reported to modulate the H+ intercalation. The modulation of metal-O bond type and covalency degree on the average charge of O atom results in optimized ϵp and H+ adsorption energy for M-MnO2 , thus promoting the balance between H+ adsorption and desorption, which plays a determinant role on H+ intercalation. The optimized Cu-MnO2 delivers superior rate capability with the capacity of 153 mAh g-1 at a high rate of 3 A g-1 after 1000 cycles. This work demonstrates that ϵp could be a significant descriptor for H+ intercalation, and tuning ϵp effectively increases H+ intercalation contribution with excellent rate capability in ZIBs.

Proton Intercalation/De-intercalation Chemistry in Phenazine-based Anode for Hydronium-ion Batteries.

Hydronium-ion batteries have received significant attention owing to the merits of extraordinary sustainability and excellent rate abilities. However, achieving high-performance hydronium-ion batteries remains a challenge due to the inferior properties of anode materials in strong acid electrolyte. Herein, a hydronium-ion battery is constructed which is based on a diquinoxalino [2,3-a:2',3'-c] phenazine (HATN) anode and a MnO2 @graphite felt cathode in a hybrid acidic electrolyte. The fast kinetics of hydronium-ion insertion/extraction into HATN electrode endows the HATN//MnO2 @GF battery with enhanced electrochemical performance. This battery exhibits an excellent rate performance (266 mAh g-1 at 0.5 A g-1 , 97 mAh g-1 at 50 A g-1 ), attractive energy density (182.1 Wh kg-1 ) and power density (31.2 kW kg-1 ), along with long-term cycle stability. These results shed light on the development of advanced hydronium-ion batteries.

Confining ZnS/SnS2 Ultrathin Heterostructured Nanosheets in Hollow N-Doped Carbon Nanocubes as Novel Sulfur Host for Advanced Li-S Batteries.

Hollow nanostructured hosts are important scaffolds to achieve high sulfur loading, fast charge transfer, and conspicuous restraint of lithium polysulfides (LiPSs) shuttling in lithium-sulfur (Li-S) batteries. However, developing high-efficiency hollow hosts for improving utilization and conversion of aggregated sulfur in the hollow chamber remains a longstanding challenge. Herein, hollow N-doped carbon nanocubes confined petal-like ZnS/SnS2 heterostructures (ZnS/SnS2 @NC) as a conceptually novel host for Li-S batteries are reported. Specifically, compared to consubstantial hollow double-shelled hosts, the ZnS/SnS2 @NC with higher effective active surface area brings dense contact with sulfur and enhances efficient adsorption sites for binding LiPSs and accelerating their conversion. Benefiting from the unique structure and sophisticated composition, the resulting S@ZnS/SnS2 @NC cathodes exhibit 1294 mAh g-1 at 0.2 C, an ultralow capacity decay of 0.016% per cycle over 500 cycles at 1.0 C, and a high area capacity of 4.77 mAh cm-2 at 0.5 C (5.9 mg cm-2 ). Meanwhile, the performance evolution of S@ZnS/SnS2 @NC cathodes under various sulfur loadings is further investigated by using EIS, which provides the beneficial guidance to explore viable strategies further optimizing their performance. This work sheds new insights into the design of hollow nanostructured hosts with a distinguished ability to regulate LiPSs in Li-S batteries.

Flexible core/shelled PPy@PANI nanotube porous films for hybrid supercapacitors.

Flexibility of the films and the limited ion transport in the vertical direction of film highly restrict the development of flexible supercapacitors. Herein, we have developed hybrid porous films consisting of N-doped holey graphene nanosheets (NHGR) with abundant in-plane nanopores and the vertically aligned polyaniline nanowires arrays on polypyrrole nanotubes (PPy@PANI) via a two-step oxidative polymerization strategy and vacuum filtration. The rational design can efficiently shorten the diffusion path of electrons/ions, alleviate volume variation of electrodes during cycling, enhance electric conductivity of the hybrids, and while offer abundant active interfacial sites for electrochemical reaction. Benefiting from the distinctive structural and compositional merits, the obtained PPy@PANI/NHGR film electrode manifests an excellent electrochemical properties in terms of specific capacity (1348 mF cm-2at a current density of 1 mA cm-2), rate capability (81.2% capacitance retention from 1 to 30 mA cm-2), and cycling stability (capacitance retention of 73.7% at 20 mA cm-2after 7000 cycles). Matched with NHGR negative electrode, the assembled flexible all-solid-state asymmetric supercapacitor displays a remarkable areal capacitance of 359 mF cm-2at 5 mA cm-2, maximum areal energy density of 112.2µWh cm-2at 3.747 mW cm-2, and good flexibility at various bending angles while preserving stable cycling performance. The result shows the PPy@PANI/NHGR film with high flexibility and 3D ions transport channels is highly attractive for flexible energy storage devices.

Building Fast Diffusion Channel by Constructing Metal Sulfide/Metal Selenide Heterostructures for High-Performance Sodium Ion Batteries Anode.

Heterostructure engineering is one of the most promising modification strategies toward improving sluggish kinetics for the anode of sodium ion batteries (SIBs). Herein, we report a systemic investigation on the different types of heterostructure interfaces' effects of discharging products (Na2O, Na2S, Na2Se) on the rate performance. First-principle calculations reveal that the Na2S/Na2Se interface possesses the lowest diffusion energy barrier (0.39 eV) of Na among three kinds of interface structures (Na2O/Na2S, Na2O/Na2Se, and Na2S/Na2Se) due to its smallest recorded interface deformation, similar electronegativity, and lattice constant. The experimental evidence confirms that the metal sulfide/metal selenide (SnS/SnSe2) hierarchical anode exhibits outstanding rate performance, where the normalized capacity at 10 A g-1 compared to 0.1 A g-1 is 45.6%. The proposed design strategy in this work is helpful to design high rate performance anodes for advanced battery systems.

Uniform ß-Na0.33V2O5 nanorod cathode providing superior rate capability for lithium ion batteries.

A vanadium bronze nanomaterial, ß-Na0.33V2O5, was synthesized using a facile sol-gel method followed by annealing at high temperature. The morphology of the sample was observed using a scanning electron microscope (SEM) and a transmission electron microscope (TEM), and the crystal phase was determined by x-ray diffraction (XRD) spectroscopy. The as-prepared sample displays a morphology of nanorods, and has a pure phase with a high crystallinity. When used as the cathode material for rechargeable lithium batteries, the ß-Na0.33V2O5 nanorods fired at 400 °C exhibit better electrochemical properties at a 2.0 V cutoff voltage than those at a 1.5 V cutoff voltage. Over the voltage range of 2.0-4.0 V, they can deliver an initial capacity of 221 mAh g-1 at a 0.5 C rate, and retain 212 mAh g-1 after 200 cycles, accounting for a capacity fading of only 0.02% per cycle. At a 5 C rate, the discharge capacity still reaches 146 mAh g-1, displaying an outstanding rate capability. Control of the electrochemical window is proved to be an effective strategy in boosting the cycling stability of the ß-Na0.33V2O5 cathode in this work in spite of a discounted capacity. Results suggest the as-prepared ß-Na0.33V2O5 nanorods are promising for use as high-performance cathode materials for rechargeable lithium batteries.

Unique Double-Interstitialcy Mechanism and Interfacial Storage Mechanism in the Graphene/Metal Oxide as the Anode for Sodium-Ion Batteries.

Graphene/metal oxides (G/MO) composite materials have attracted much attention as the anode of sodium ion batteries (SIBs), because of the high theoretical capacity. However, most metal oxides operate based on the conversion mechanism and the alloying mechanism has changed to Na2O after the first cycle. The influence of G/Na2O (G/N) on the subsequent sodiation process has never been clearly elucidated. In this work, we report a systematic investigation on the G/N interface from both aspects of theoretical simulation and experiment characterization. By applied first-principles simulations, we find that the sluggish kinetics in the G/MO materials is mainly caused by the high diffusion barrier (0.51 eV) inside the Na2O bulk, while the G/N interface shows a much faster transport kinetics (0.25 eV) via unique double-interstitialcy mechanism. G/N interface possesses an interfacial storage of Na atom through the charge separation mechanism. The experimental evidence confirms that high interfacial ratio structure of G/N greatly improves the rate performance and endows G/MO materials the interfacial storage. Furthermore, the experimental investigation finds that the high interfacial ratio structure of G/N also benefits from the reversible reaction between SnO2 and Sn during cycling. Lastly, the effects of (N, O, S) doping in graphene systems at the G/N interface were also explored. This work provides a fundamental comprehension on the G/MO interface structure during the sodiation process, which is helpful to design energy storage materials with high rate performance and large capacity.

Three-Dimensional Ordered Macroporous Metal-Organic Framework Single Crystal-Derived Nitrogen-Doped Hierarchical Porous Carbon for High-Performance Potassium-Ion Batteries.

The biggest challenge of potassium-ion batteries (KIBs) application is to develop high-performance electrode materials to accommodate the potassium ions large size. Herein, by rational design, we carbonize three-dimensional (3D) ordered macroporous ZIF-8 to fabricate 3D interconnected nitrogen-doped hierarchical porous carbon (N-HPC) that shows excellent rate performance (94 mAh g-1 at 10.0 A g-1), unprecedented cycle stability (157 mA g-1 after 12000 cycles at 2.0 A g-1), and superior reversible capacity (292 mAh g-1 at 0.1 A g-1). The 3D hierarchical porous structure diminishes the diffusion distance for both ions/electrons, while N-doping improves the reactivity and electronic conductivity via producing more defects. In addition, the bicontinuous structure possesses a large specific surface area, decreasing the current density, again improving the rate performance. In situ Raman spectra analysis confirms the potassiation and depotassiation in the N-HPC are highly reversible processes. The galvanostatic intermittent titration measurement and first-principles calculations reveal that the interconnected macropores are more beneficial to the diffusion of the K+. This 3D interpenetrating structure demonstrates a superiority for energy storage applications.

Mesoporous ZnCo2O4/rGO nanocomposites enhancing sodium storage.

In this study, mesoporous ZnCo2O4/rGO nanocomposites were favorably synthesized via a simple solvothermal technique. As a prospective anode material for sodium-ion batteries, the resulting ZnCo2O4/rGO-II nanocomposite exhibited superior electrochemical sodium storage performance with predominant specific capacity, favorable cyclability and ascendant rate capability. For example, an outstanding discharge capacity of 210.5 mAh g-1 was delivered at a current density of 200 mA g-1. Notably, the nanocomposite could yield a discharge capacity of 101.7 mAh g-1 at a current density of 1000 mA g-1 after 500 loops, which certifies its superior capacity retention and predominant cycling stability. The boosted performance of the anode materials is due to the mutual synergistic effect resulting from a combination of the mesoporous ZnCo2O4 nanospheres and conducting reduced graphene oxide nanosheets.

Recent Advances in Layered Ti3 C2 Tx MXene for Electrochemical Energy Storage.

Ti3 C2 Tx , a typical representative among the emerging family of 2D layered transition metal carbides and/or nitrides referred to as MXenes, has exhibited multiple advantages including metallic conductivity, a plastic layer structure, small band gaps, and the hydrophilic nature of its functionalized surface. As a result, this 2D material is intensively investigated for application in the energy storage field. The composition, morphology and texture, surface chemistry, and structural configuration of Ti3 C2 Tx directly influence its electrochemical performance, e.g., the use of a well-designed 2D Ti3 C2 Tx as a rechargeable battery anode has significantly enhanced battery performance by providing more chemically active interfaces, shortened ion-diffusion lengths, and improved in-plane carrier/charge-transport kinetics. Some recent progresses of Ti3 C2 Tx MXene are achieved in energy storage. This Review summarizes recent advances in the synthesis and electrochemical energy storage applications of Ti3 C2 Tx MXene including supercapacitors, lithium-ion batteries, sodium-ion batteries, and lithium-sulfur batteries. The current opportunities and future challenges of Ti3 C2 Tx MXene are addressed for energy-storage devices. This Review seeks to provide a rational and in-depth understanding of the relation between the electrochemical performance and the nanostructural/chemical composition of Ti3 C2 Tx , which will promote the further development of 2D MXenes in energy-storage applications.

Selective Etching Induced Synthesis of Hollow Rh Nanospheres Electrocatalyst for Alcohol Oxidation Reactions.

The hollow noble metal nanostructures have attracted wide attention in catalysis/electrocatalysis. Here a two-step procedure for constructing hollow Rh nanospheres (Rh H-NSs) with clean surface is described. By selectively removing the surfactant and Au core of Au-core@Rh-shell nanostructures (Au@Rh NSs), the surface-cleaned Rh H-NSs are obtained, which contain abundant porous channels and large specific surface area. The as-prepared Rh H-NSs exhibit enhanced inherent activity for the methanol oxidation reaction (MOR) compared to state-of-the-art Pt nanoparticles in alkaline media. Further electrochemical experiments show that Rh H-NSs also have high activity for the electrooxidation of formaldehyde and formate (intermediate species in the course of the MOR) in alkaline media. Unfortunately, Rh H-NSs have low electrocatalytic activity for the ethanol and 1-propanol oxidation reactions in alkaline media. All electrochemical results indicate that the order of electrocatalytic activity of Rh H-NSs for alcohol oxidation reaction is methanol (C1 ) > ethanol (C2 ) > 1-propanol (C3 ). This work highlights the synthesis route of Rh hollow nanostructures, and indicates the promising application of Rh nanostructures in alkaline direct methanol fuel cells.

Vertically Aligned Co9 S8 Nanotube Arrays onto Graphene Papers as High-Performance Flexible Electrodes for Supercapacitors.

Paper-like electrodes are emerging as a new category of advanced electrodes for flexible supercapacitors (SCs). Graphene, a promising two-dimensional material with high conductivity, can be easily processed into papers. Here, we report a rational design of flexible architecture with Co9 S8 nanotube arrays (NAs) grown onto graphene paper (GP) via a facile two-step hydrothermal method. When employed as flexible free-standing electrode for SCs, the proposed architectured Co9 S8 /GPs exhibits superior electrochemical performance with ultrahigh capacitance and outstanding rate capability (469 F g-1 at 10 A g-1 ). These results demonstrate that the new nanostructured Co9 S8 /GPs can be potentially applied in high performance flexible supercapacitors.

Key Roles of Interfaces in Inverted Metal-Halide Perovskite Solar Cells.

Metal-halide perovskite solar cells (PSCs), an emerging technology for transforming solar energy into a clean source of electricity, have reached efficiency levels comparable to those of commercial silicon cells. Compared with other types of PSCs, inverted perovskite solar cells (IPSCs) have shown promise with regard to commercialization due to their facile fabrication and excellent optoelectronic properties. The interlayer interfaces play an important role in the performance of perovskite cells, not only affecting charge transfer and transport, but also acting as a barrier against oxygen and moisture permeation. Herein, we describe and summarize the last three years of studies that summarize the advantages of interface engineering-based advances for the commercialization of IPSCs. This review includes a brief introduction of the structure and working principle of IPSCs, and analyzes how interfaces affect the performance of IPSC devices from the perspective of photovoltaic performance and device lifetime. In addition, a comprehensive summary of various interface engineering approaches to solving these problems and challenges in IPSCs, including the use of interlayers, interface modification, defect passivation, and others, is summarized. Moreover, based upon current developments and breakthroughs, fundamental and engineering perspectives on future commercialization pathways are provided for the innovation and design of next-generation IPSCs.

MXene Key Composites: A New Arena for Gas Sensors.

With the development of science and technology, the scale of industrial production continues to grow, and the types and quantities of gas raw materials used in industrial production and produced during the production process are also constantly increasing. These gases include flammable and explosive gases, and even contain toxic gases. Therefore, it is very important and necessary for gas sensors to detect and monitor these gases quickly and accurately. In recent years, a new two-dimensional material called MXene has attracted widespread attention in various applications. Their abundant surface functional groups and sites, excellent current conductivity, tunable surface chemistry, and outstanding stability make them promising for gas sensor applications. Since the birth of MXene materials, researchers have utilized the efficient and convenient solution etching preparation, high flexibility, and easily functionalize MXene with other materials to prepare composites for gas sensing. This has opened a new chapter in high-performance gas sensing materials and provided a new approach for advanced sensor research. However, previous reviews on MXene-based composite materials in gas sensing only focused on the performance of gas sensing, without systematically explaining the gas sensing mechanisms generated by different gases, as well as summarizing and predicting the advantages and disadvantages of MXene-based composite materials. This article reviews the latest progress in the application of MXene-based composite materials in gas sensing. Firstly, a brief summary was given of the commonly used methods for preparing gas sensing device structures, followed by an introduction to the key attributes of MXene related to gas sensing performance. This article focuses on the performance of MXene-based composite materials used for gas sensing, such as MXene/graphene, MXene/Metal oxide, MXene/Transition metal sulfides (TMDs), MXene/Metal-organic framework (MOF), MXene/Polymer. It summarizes the advantages and disadvantages of MXene composite materials with different composites and discusses the possible gas sensing mechanisms of MXene-based composite materials for different gases. Finally, future directions and inroads of MXenes-based composites in gas sensing are presented and discussed.