Realizing Efficient Activity and High Conductivity of Perovskite Symmetrical Electrode by Vanadium Doping for CO2 Electrolysis.

Solid oxide electrolysis cells (SOECs) show significant promise in converting CO2 to valuable fuels and chemicals, yet exploiting efficient electrode materials poses a great challenge. Perovskite oxides, known for their stability as SOEC electrodes, require improvements in electrocatalytic activity and conductivity. Herein, vanadium(V) cation is newly introduced into the B-site of Sr2Fe1.5Mo0.5O6-δ perovskite to promote its electrochemical performance. The substitution of variable valence V5+ for Mo6+ along with the creation of oxygen vacancies contribute to improved electronic conductivity and enhanced electrocatalytic activity for CO2 reduction. Notably, the Sr2Fe1.5Mo0.4V0.1O6-δ based symmetrical SOEC achieves a current density of 1.56 A cm-2 at 1.5 V and 800 °C, maintaining outstanding durability over 300 h. Theoretical analysis unveils that V-doping facilitates the formation of oxygen vacancies, resulting in high intrinsic electrocatalytic activity for CO2 reduction. These findings present a viable and facile strategy for advancing electrocatalysts in CO2 conversion technologies.

Construction of hierarchical In2O3/In2S3-ZnCdS ternary microsphere heterostructures for efficient photocatalytic nitrogen fixation.

Photocatalytic ammonia production holds immense promise as an environmentally sustainable approach to nitrogen fixation. In this study, In2O3/In2S3-ZnCdS ternary heterostructures were successfully constructed through an innovative in situ anion exchange process, coupled with a low-temperature hydrothermal method for ZnCdS (ZCS) incorporation. The resulting In2O3/In2S3-ZCS photocatalyst was proved to be highly efficient in converting N2 to NH3 under mild conditions, eliminating the need for sacrificial agents or precious metal catalysts. Notably, the NH4+ yield of In2O3/In2S3-0.5ZCS reached a significant level of 71.2 µmol g-1 h-1, which was 10.47 times higher than that of In2O3 (6.8 µmol g-1 h-1) and 3.22 times higher than that of In2O3/In2S3 (22.1 µmol g-1 h-1). This outstanding performance can be attributed to the ternary heterojunction configuration, which significantly extends the lifetime of photogenerated carriers and enhances the spatial separation of electrons and holes. The synergistic interplay between CdZnS, In2S3, and In2O3 in the heterojunction facilitates electron transport, thereby boosting the rate of the photocatalytic nitrogen fixation reaction. Our study not only validates the efficacy of ternary heterojunctions in photocatalytic nitrogen fixation but also offers valuable insights for the design and construction of such catalysts for future applications.

A Dual-Carbon Potassium-Ion Capacitor Enabled by Hollow Carbon Fibrous Electrodes with Reduced Graphitization.

The large size of K+ ions (1.38 Å) sets a challenge in achieving high kinetics and long lifespan of potassium storage devices. Here, a fibrous ZrO2 membrane is utilized as a reactive template to construct a dual-carbon K-ion capacitor. Unlike graphite, ZrO2-catalyzed graphitic carbon presents a relatively disordered layer arrangement with an expanded interlayer spacing of 0.378 nm to accommodate K+ insertion/extraction. Pyridine-derived nitrogen sites can locally store K-ions without disrupting the formation of stage-1 graphite intercalation compounds (GICs). Consequently, N-doped hollow graphitic carbon fiber achieves a K+-storage capacity (primarily below 1 V), which is 1.5 time that of commercial graphite. Potassium-ion hybrid capacitors are assembled using the hollow carbon fiber electrodes and the ZrO2 nanofiber membrane as the separator. The capacitor exhibits a high power of 40 000 W kg-1, full charge in 8.5 s, 93% capacity retention after 5000 cycles at 2 A g-1, and a low self-discharge rate of 8.6 mV h-1. The scalability and high performance of the lattice-expanded tubular carbon electrodes underscores may advance the practical potassium-ion capacitors.

Attapulgite-intercalated g-C3N4/ZnIn2S4 3D hierarchical Z-scheme heterojunction for boosting photocatalytic hydrogen production.

Construction of hierarchical architecture with suitable band alignment for graphitic carbon nitride (g-C3N4) played a pivotal role in enhancing the efficiency of photocatalysts. In this study, a novel attapulgite-intercalated g-C3N4/ZnIn2S4 nanocomposite material (ZIS/CN/ATP, abbreviated as ZCA) was successfully synthesized using the freeze-drying technique, thermal polymerization, and a simple low-temperature hydrothermal method. Attapulgite (ATP) was intercalated into g-C3N4 to effectively regulate its interlayer structure. The results reveal a substantial enlargement of its internal space, thereby facilitating the provision of additional active sites for improved dispersibility of ZnIn2S4. Notably, the optimized photocatalyst, comprising a mass ratio of ATP, g-C3N4, and ZnIn2S4 at 1:1:2.5 respectively, achieves an outstanding hydrogen evolution rate of 3906.15 µmol g-1h-1, without the need for a Pt co-catalyst. This rate surpasses that of pristine g-C3N4 by a factor of 475 and ZnIn2S4 by a factor of 5, representing a significant improvement in performance. This significant enhancement can be primarily attributed to the higher specific surface area, richer active sites, broadened light response range, and efficient interfacial charge transfer channels of the ZCA composite photocatalyst. Furthermore, the Z-scheme photocatalytic mechanism for the sandwich-like layered structure heterojunction was thoroughly investigated using diverse characterization techniques. This work offers new insights for enhancing photocatalytic performance through the expanded utilization of natural minerals, paving the way for future advancements in this field.

Ultrasensitive monitoring of PCB77 in environmental samples using a visible-driven photoelectrochemical sensing platform coupling with exonuclease I assisted in target recycling.

Due to the urgent need for detecting trace amounts of 3,3',4,4'-tetrachlorobiphenyl (PCB77) in the environment, we have developed an efficient and visible-driven photoelectrochemical (PEC) sensing platform based on carbon quantum dots (CQDs) modified titanium dioxide nanorods (TiO2 NRs), coupling with exonuclease I (Exo I) assisted in target recycling for significant signal amplification. CQDs/TiO2 NRs with high visible-light absorption ability and electron-hole separation efficiency is used as photoactive substrate for anchoring anti-PCB77 aptamer and its complementary DNA (cDNA). With the addition of PCB77, the specific interaction between PCB77 and its aptamer forces aptamer to separate from the electrode surface, resulting in an increase in photocurrent density. Adding Exo I in the test system, a self-catalytic target cycle was motivated, which significantly increased the PEC signal by more than twice, achieving signal amplification. The relationship between the photocurrent density changes and the concentrations of PCB77 are utilized to achieve quantitative detection of PCB77. The designed PEC sensing platform has good analytical performance with a detection limit as low as 0.33 pg L-1, high selectivity and stability. Moreover, the PEC sensor is successfully used to evaluate the content of PBC77 in the environment samples. The established sensing platform provides a simple and efficient method for detecting trace amounts of PCB77 in the environment.

Recent Advancements of Graphene-Based Materials for Zinc-Based Batteries: Beyond Lithium-Ion Batteries.

Graphene-based materials (GBMs) possess a unique set of properties including tunable interlayer channels, high specific surface area, and good electrical conductivity characteristics, making it a promising material of choice for making electrode in rechargeable batteries. Lithium-ion batteries (LIBs) currently dominate the commercial rechargeable battery market, but their further development has been hampered by limited lithium resources, high lithium costs, and organic electrolyte safety concerns. From the performance, safety, and cost aspects, zinc-based rechargeable batteries have become a promising alternative of rechargeable batteries. This review highlights recent advancements and development of a variety of graphene derivative-based materials and its composites, with a focus on their potential applications in rechargeable batteries such as LIBs, zinc-air batteries (ZABs), zinc-ion batteries (ZIBs), and zinc-iodine batteries (Zn-I2 Bs). Finally, there is an outlook on the challenges and future directions of this great potential research field.

Atomistic Insights into Medium-Entropy Perovskites for Efficient and Robust CO2 Electrolysis.

Solid oxide electrolysis cells (SOECs) show great promise in converting CO2 to valuable products. However, their practicality for the CO2 reduction reaction (CO2RR) is restricted by sluggish kinetics and limited durability. Herein, we propose a novel medium-entropy perovskite, Sr2(Fe1.0Ti0.25Cr0.25Mn0.25Mo0.25)O6-δ (SFTCMM), as a potential electrode material for symmetrical SOEC toward CO2RR. Experimental and theoretical results unveil that the configuration entropy of SFTCMM perovskites contributes to the strengthened metal 3d-O 2p hybridization and the reduced O 2p bond center. This variation of electronic structure benefits oxygen vacancy creation and diffusion as well as CO2 adsorption and activation and ultimately accelerates CO2RR and oxygen electrocatalysis kinetics. Notably, the SFTCMM-based symmetrical SOEC delivers an excellent current density of 1.50 A cm-2 at 800 °C and 1.5 V, surpassing the prototype Sr2Fe1.5Mo0.5O6-δ (SFM, 1.04 A cm-2) and most of the state-of-the-art electrodes for symmetrical SOECs. Moreover, the SFTCMM-based symmetrical SOEC demonstrates stable CO2RR operation for 160 h.

Ultrastable Graphite-Potassium Anode through Binder Chemistry.

Graphite with abundant reserves has attracted enormous research interest as an anode of potassium-ion batteries (PIBs) owing to its high plateau capacity of 279 mAh g-1 at ≈0.2 V in conventional carbonate electrolytes. Unfortunately, it suffers from fast capacity decay during K+ storage. Herein, an ultrastable graphite-potassium anode is developed through binder chemistry. Polyvinyl alcohol (PVA) is utilized as a water-soluble binder to generate a uniform and robust KF-rich SEI film on the graphite surface, which can not only inhibit the electrolyte decomposition, but also withstand large volume expansion during K+ -insertion. Compared to the PVDF as binder, PVA-based graphite anode can operate for over 2000 cycles (running time of 406 days at C/3) with 97% capacity retention in KPF6 -based electrolytes. The initial Coulombic efficiency (ICE) of graphite anode is as high as 81.6% using PVA as the binder, higher than that of PVDF (40.1%). Benefiting from the strong adhesion ability of PVA, a graphite||fluorophosphate K-ion full battery is further built through 3D printing, which achieves a record-high areal energy of 8.9 mWh cm-2 at a total mass loading of 38 mg cm-2 . These results demonstrate the important role of binder in developing high-performance PIBs.

3D printing of hierarchically micro/nanostructured electrodes for high-performance rechargeable batteries.

3D printing, also known as additive manufacturing, is capable of fabricating 3D hierarchical micro/nanostructures by depositing a layer-upon-layer of precursor materials and solvent-based inks under the assistance of computer-aided design (CAD) files. 3D printing has been employed to construct 3D hierarchically micro/nanostructured electrodes for rechargeable batteries, endowing them with high specific surface areas, short ion transport lengths, and high mass loading. This review summarizes the advantages and limitations of various 3D printing methods and presents the recent developments of 3D-printed electrodes in rechargeable batteries, such as lithium-ion batteries, sodium-ion batteries, and lithium-sulfur batteries. Furthermore, the challenges and perspectives of the 3D printing technique for electrodes and rechargeable batteries are put forward. This review will provide new insight into the 3D printing of hierarchically micro/nanostructured electrodes in rechargeable batteries and promote the development of 3D printed electrodes and batteries in the future.

Coupling MnS and CoS Nanocrystals on Self-Supported Porous N-doped Carbon Nanofibers to Enhance Oxygen Electrocatalytic Performance for Flexible Zn-Air Batteries.

Seeking highly efficient, stable, and cost-effective bifunctional electrocatalysts of rechargeable Zn-air batteries (ZABs) is the top-priority for developing new generation portable electronic devices. For this, the rational and effective structural design, interface engineering, and electron recombination on electrocatalysts should be taken into account to reduce the reaction overpotential and expedite the kinetics of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Herein, we construct a MnCo-based metal organic framework-derived heterogeneous MnS-CoS nanocrystals, which are anchored on free-standing porous N-doped carbon fibers (PNCFs) by the in situ growth method and vulcanization process. Benefiting from the abundant vacancies and active sites, strong interfacial coupling as well as favorable conductivity, the MnS-CoS/PNCFs composite electrode delivers a mentionable oxygen electrocatalytic activity and stability with a half-wave potential of 0.81 V for ORR and an overpotential of 350 mV for OER in the alkaline medium. Of note, the flexible rechargeable ZAB using MnS-CoS/PNCFs as binder-free air cathode offers high power density of 86.7 mW cm-2, large specific capacity of 563 mA h g-1, and adapts to different bending degree of operation. In addition, the density functional theory calculation clarifies that the heterogeneous MnS-CoS nanocrystals reduces the reaction barrier and enhances the conductivity of the catalyst and the adsorption capacity of the intermediates during the ORR and OER process. This study opens up a new insight to the design of the self-supported air cathode for flexible electronic devices.

Functionalized Halloysite Scaffold Controls Sodium Dendrite Growth.

Sodium metal is one of the most promising anodes for the prospective low-cost rechargeable batteries. Nevertheless, the commercialization of Na metal anodes remains restricted by sodium dendrite growth. Herein, halloysite nanotubes (HNTs) were chosen as the insulated scaffolds, and Ag nanoparticles were introduced as sodiophilic sites to achieve uniform sodium deposition from bottom to top under the synergistic effect. Density functional theory (DFT) calculation results demonstrated that the presence of Ag greatly increased the binding energy of sodium on HNTs/Ag (-2.85 eV) vs HNTs (-0.85 eV). Meanwhile, thanks to the opposite charges on the inner and outer surfaces of HNTs, faster Na+ transfer kinetics and selective adsorption of SO3CF3- on the inner surface of HNTs were achieved, thus avoiding the formation of space charge. Accordingly, the coordination between HNTs and Ag afforded a high Coulombic efficiency (about 99.6% at 2 mA cm-2), long lifespan in a symmetric battery (for over 3500 h at 1 mA cm-2), and remarkable cycle stability in Na metal full batteries. This work offers a novel strategy to design a sodiophilic scaffold by nanoclay for dendrite-free Na metal anodes.

Cross-Linked Sodium Alginate as A Multifunctional Binder to Achieve High-Rate and Long-Cycle Stability for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) hold great promise owing to the naturally abundant sodium resource and high safety. The research focus of SIBs is usually directed toward electrode materials, while the binder as an important component is rarely investigated. Herein, a cross-linked sodium alginate (SA)/graphene oxide (GO) binder is judiciously designed to serve as a robust artificial interphase on the surface of both anode and cathode of SIBs. Benefiting from the cross-linking continuous network structure as well as the highly hydrophilic nature, the SA-GO binder possesses a large tensile strength of 197.7 Mpa and a high ionic conductivity of 0.136 mS cm-1 , superior to pure SA (93.8 Mpa, 0.025 mS cm-1 ). Moreover, the structural design of SA-GO binder exhibits a strong binding ability to guarantee structural integrity during cycling. To demonstrate its effectiveness, polyanion-type phosphates (e.g., Na3 (VO)2 (PO4 )2 F) and chalcogenides (e.g., MoS2 , VS2 ) are adopted as cathode and anode materials of SIBs, respectively. As compared to traditional binders (e.g., PVDF, SA), electrodes with the SA-GO binder exhibits significantly increased rate capability and cycling stability, such as Na3 (VO)2 (PO4 )2 F (40 C fast-charge, 84% capacity retention after 1000 cycles). This work highlights the role of novel aqueous-based binders in developing next-generation sodium-storage devices.

Rationally designing a Ti3C2Tx/CNTs-Co9S8 heterostructure as a sulfur host with multi-functionality for high-performance lithium-sulfur batteries.

Lithium-sulfur (Li-S) batteries have been regarded as potential next-generation batteries owing to their ultrahigh theoretical capacity and abundance of sulfur. However, polysulfide shuttling, poor electronic conductivity, and severe volume expansion limit their commercial prospects. In this work, we rationally constructed a 3D porous Ti3C2Tx/CNTs-Co9S8 heterostructure derived from a zeolite imidazole framework (ZIF)/Ti3C2Tx MXene composite via carbonization and subsequent sulfidation. In this 3D porous Ti3C2Tx/CNTs-Co9S8 heterostructure, the 3D porous Ti3C2Tx MXene structure can provide facilitated ion and electron transport, good structural stability, and polar bonds to anchor sulfur and polysulfides. The formed CNTs can enhance ion diffusion and electron transport. The Co9S8 nanoparticles can accelerate the conversion reaction of polysulfides to Li2S, which can further prevent polysulfide shuttling. The 3D porous structure can buffer the electrode volume change upon cycling. This rationally designed Ti3C2Tx/CNTs-Co9S8/S cathode exhibits a high initial capacity of 1389.8 mA h g-1 at 0.1C, good cyclic stability (730.7 mA h g-1 at 0.2C after 100 cycles), and excellent rate capacities (530.7 mA h g-1 at 1C). When the S loading was 2.5 mg cm-2, the Ti3C2Tx/CNTs-Co9S8/S cathode still exhibited a reversible capacity of 472.8 mA h g-1 at 0.5C after 300 cycles.

A montmorillonite-modification strategy enabling long cycling stability of dual-ion batteries.

Lithium‖graphite dual-ion batteries (DIBs) have received widespread attention due to their low cost and high operating voltage (nearly 5 V). However, DIBs face several challenges such as decomposition of the electrolyte under high voltage and structural deterioration of graphite. Herein, montmorillonite (MMT) is employed to generate a favorable and robust cathode electrolyte interface (CEI) layer on the graphite surface. As a result, the DIBs exhibit a 100% capacity retention for 500 cycles at 2C. Even after 1000 cycles at 5C, the capacity retention is still as high as 99%.

Hierarchical MXene/transition metal oxide heterostructures for rechargeable batteries, capacitors, and capacitive deionization.

2D MXenes have attracted considerable attention due to their high electronic conductivity, tunable metal compositions, functional termination groups, low ion diffusion barriers, and abundant active sites. However, MXenes suffer from sheet stacking and partial surface oxidation, limiting their energy storage and water treatment development. To solve these problems and enhance the performance of MXenes in practical applications, various hierarchical MXene/transition metal oxide (MXene/TMO) heterostructures are rationally designed and constructed. The hierarchical MXene/TMO heterostructures can not only prevent the stacking of MXene sheets and improve the electronic conductivity and buffer the volume change of TMOs during the electrochemical reaction process. The synergistic effect of conductive MXenes and active TMOs also makes MXene/TMO heterostructures promising electrode materials for energy storage and seawater desalination. This review mainly introduces and discusses the recent research progress in MXene/TMO heterostructures, focusing on their synthetic strategies, heterointerface engineering, and applications in rechargeable batteries, capacitors, and capacitive deionization (CDI). Finally, the key challenges and prospects for the future development of the MXene/TMO heterostructures in rechargeable batteries, capacitors, and CDI are proposed.

A Mechanically Flexible Necklace-Like Architecture for Achieving Fast Charging and High Capacity in Advanced Lithium-Ion Capacitors.

Integration of fast charging, high capacity, and mechanical flexibility into one electrode is highly desired for portable energy-storage devices. However, a high charging rate is always accompanied by capacity decay and cycling instability. Here, a necklace-structured composite membrane consisting of micron-sized FeSe2 cubes uniformly threaded by carbon nanofibers (CNF) is reported. This unique electrode configuration can not only accommodate the volumetric expansion of FeSe2 during the lithiation/delithiation processes for structural robustness but also guarantee ultrafast kinetics for Li+ entry. At a high mass loading of 6.2 mg cm-2 , the necklace-like FeSe2 @CNF electrode exhibits exceptional rate capability (80.7% capacity retention from 0.1 to 10 A g-1 ) and long-term cycling stability (no capacity decay after 1100 charge-discharge cycles at 2 A g-1 ). The flexible lithium-ion capacitor (LIC) fabricated by coupling a pre-lithiated FeSe2 @CNF anode with a porous carbon cathode delivers impressive volumetric energy//power densities (98.4 Wh L-1 at 157.1 W L-1 , and 58.9 Wh L-1 at 15714.3 W L-1 ). The top performance, long-term cycling stability, low self-discharge rate, and high mechanical flexibility make it among the best LICs ever reported.

Metal organic framework derived perovskite/spinel heterojunction as efficient bifunctional oxygen electrocatalyst for rechargeable and flexible Zn-air batteries.

Interface engineering strategy has been developed to design efficient catalysts for boosting electrocatalytic performance in past few decades. Herein, heterojunctions of PrCoO3/Co3O4 nanocages (PCO/Co3O4 NCs) with atomic-level engineered interfaces and rich oxygen vacancies are proposed for Zn-air batteries. The synthesized product shows exceptional bifunctional activity and robust stability towards oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The enhanced catalytic capacity is primary attributed to the synergistic effect of PCO/Co3O4, evidenced by the experimental results and theoretical calculations. More importantly, the PCO/Co3O4 NCs assembled liquid Zn-air battery exhibits a power density of 182 mW cm-2 and a long-term operation of 185 h. When assembled into solid-state cable type battery, this newly designed catalyst also reaches a stable open circuit voltage (1.359 V) and a peak power density of 85 mW cm-3. Our findings provide essential guidelines of engineering heterostructured electrocatalysts for future wearable electronic devices.

Natural ore molybdenite as a high-capacity and cheap anode material for advanced lithium-ion capacitors.

Hybrid lithium-ion capacitors (LICs) receive special interests because they work by combining the merits of high-capacity lithium-ion batteries and high-rate capacitors in a Li salt containing electrolyte, so as to bridge the gap between the two devices. One of main challenges for LICs is to develop inexpensive and superior anode materials at high rates. In this work, natural molybdenite was utilized as precursor to achieve the scalable production of cheap MoS2/carbon composites. This molybdenite-derived MoS2/carbon electrode can not only exhibit excellent Li+-storage performances including ultrahigh specific capacity (1427 mAh g-1after 1000 cycles at 1 A g-1) and rate capability (554 mAh g-1at 10 A g-1), but also possess four-times higher tap density than that of commercial graphite. By employing MoS2/carbon as the anode and activated carbon as the cathode, the as-assembled LIC device delivers both high energy//high power density and long cycle lifespan. Furthermore, the price is nearly 200 orders of magnitude lower than the traditional high-purity chemicals, which can be easily scaled up to achieve high-throughput production.

Rational design of all-solid-state TiO2-x/Cu/ZnO Z-scheme heterojunction via ALD-assistance for enhanced photocatalytic activity.

Poor visible light utilization and charge separation efficiency of TiO2 restrict its extensive application in the photocatalytic field. Herein, a specific Z-scheme TiO2-x/Cu/ZnO heterojunction was successfully constructed by atomic layer deposition (ALD) technique and spray pyrolysis technology. Benefited from the surface plasmon resonance (SPR) effect of Cu and Z-scheme heterojunction, the visible light absorption capacity was greatly enhanced. Meanwhile, ZnO nanolayer coating, prepared by ALD technique, protects Cu element to hinder its oxidation, thus enhancing the separation efficiency of photogenerated carriers. Therefore, the photocatalytic hydrogen production performance was significant improved, exhibiting a maximum value of 342.0 µmol·g-1·h-1 for the optimal B-T-0.1C-10Z (black TiO2/0.1Cu/10 nm ZnO) sample without any noble-metal cocatalyst, which is higher than pure TiO2 (310.7 µmol·g-1·h-1, with 3 wt% Pt) synthesized by spray pyrolysis method under equal conditions. In addition, a possible mechanism for the enhanced performance was briefly discussed based on the experimental results.

Hierarchical MXene/transition metal chalcogenide heterostructures for electrochemical energy storage and conversion.

MXenes have gained rapidly increasing attention owing to their two-dimensional (2D) layered structures and unique mechanical and physicochemical properties. However, MXenes have some intrinsic limitations (e.g., the restacking tendency of the 2D structure) that hinder their practical applications. Transition metal chalcogenide (TMC) materials such as SnS, NiS, MoS2, FeS2, and NiSe2 have attracted much interest for energy storage and conversion by virture of their earth-abundance, low costs, moderate overpotentials, and unique layered structures. Nonetheless, the intrinsic poor electronic conductivity and huge volume change of TMC materials during the alkali metal-ion intercalation/deintercalation process cause fast capacity fading and poor-rate and poor-cycling performances. Constructing heterostructures based on metallic conductive MXenes and highly electrochemically active TMCs is a promising and effective strategy to solve these problems and enhance the electrochemical performances. This review highlights and discusses the recent research development of MXenes and hierarchical MXene/TMC heterostructures, with a focus on the synthesis strategies, surface/heterointerface engineering, and potential applications for lithium-ion batteries, sodium-ion batteries, lithium-sulfur batteries, supercapacitors, electrocatalysis, and photocatalysis. The critical challenges and perspectives of the future development of MXenes and hierarchical MXene/TMC heterostructures for electrochemical energy storage and conversion are forecasted.