Atomically thin sheets of two‐dimensional (2D) transition metal dichalcogenides (TMDs) have attracted interest as high capacity electrode materials for electrochemical energy storage devices owing to their unique properties (high surface area, high strength and modulus, faster ion diffusion, and so on), which arise from their layered morphology and diversified chemistry. Nevertheless, low electronic conductivity, poor cycling stability, large structural changes during metal‐ion insertion/extraction along with high cost of manufacture are challenges that require further research in order for TMDs to find use in commercial batteries and supercapacitors. Here, a systematic review of cutting‐edge research focused on TMD materials beyond the widely studied molybdenum disulfide or MoS2 electrode is reported. Accordingly, a critical overview of the recent progress concerning synthesis methods, physicochemical and electrochemical properties is given. Trends and opportunities that may contribute to state‐of‐the‐art research are also discussed.

The development of feasible, scalable, and environmentally-safe electrode materials that provide stable cycling performance are critical for success of beyond lithium rechargeable batteries and supercapacitors. With respect to the sodium-ion battery (SIB) anodes constituting of transition metal dichalcogenides such as molybdenum disulfide (MoS 2 ), poor cycle stability and fast capacity degradation, due to low electronic conductivity and dissolution of chemical species in the electrolyte, hinders use of these promising layered materials as SIB anodes. Herein we report chemical functionalization in MoS 2 nanosheets with polymer-derived silicon oxycarbide or SiOC with the aim to preserve MoS 2 from dissolution in the SIB organic electrolyte, without compromising its role in sodiation and desodiation processes. Our results suggest that a MoS 2 -SiOC composite electrode is effective in bringing improved cycle stability to sodium-ion cycling over neat MoS 2 even after 100 cycles.

Sodium ion batteries (SIBs) are being billed as an economical and environmental alternative to lithium ion batteries (LIBs), especially for medium and large-scale stationery and grid storage. However, SIBs suffer from lower capacities, energy density and cycle life performance. Therefore, in order to be more efficient and feasible, novel high-performance electrodes for SIBs need to be developed and researched. This review aims to provide an exhaustive discussion about the state-of-the-art in novel high-performance anodes and cathodes being currently analyzed, and the variety of advantages they demonstrate in various critically important parameters, such as electronic conductivity, structural stability, cycle life, and reversibility.

Growing concerns regarding the safety, flammability and hazards posed by Li-ion systems have led to research on alternative rechargeable metal-ion electrochemical storage technologies. Among the most notable of these are Na-ion supercapacitors and batteries, motivated, in part, by the similar electrochemistry of Li and Na ions. However, sodium ion batteries (SIBs) come with their own set of issues, especially the large size of the Na + ion, its relatively sluggish kinetics and low energy densities. This makes the development of novel materials and appropriate electrode architecture of absolute significance. Transition metal dichalcogenides (TMDs) have attracted a lot of attention in this regard due to their relative ease of exfoliation, diverse morphologies and architectures with superior electronic properties. Here, we study the electrochemical performance of Mo-based two-dimensional (2D) layered TMDs (e.g. MoS 2 , MoSe 2 and MoTe 2 ), exfoliated in a superacid, for battery and supercapacitor applications. The exfoliated TMD flakes were interfaced with reduced graphene oxide (rGO) to be used as composite electrodes. Electron microscopy, elemental mapping and Raman spectra were used to analyse the exfoliated material and confirm the formation of 2D TMD/rGO layer morphology. For supercapacitor applications in aqueous electrolyte, the sulfide-based TMD (MoS 2 ) exhibited the best performance, providing an areal capacitance of 60.25 mF cm −2 . For SIB applications, TMD electrodes exhibited significantly higher charge capacities than the neat rGO electrode. The initial desodiation capacities for the composite electrodes are 468.84 mAh g −1 (1687.82 C g −1 ), 399.10 mAh g −1 (1436.76 C g −1 ) and 387.36 mAh g −1 (1394.49 C g −1 ) for MoS 2 , MoSe 2 and MoTe 2 , respectively. Also, the MoS 2 and MoSe 2 composite electrodes provided a coulombic efficiency of near 100 % after a few initial cycles.

Potassium-ion batteries or KIBs are prominent candidates among research involving post lithium-ion batteries due to abundant availability, low-cost, and low standard reduction potential of potassium metal. Although some chemistry correlation with other monovalent alkali metal-ion batteries may exist, research on KIB chemistry is still in its infancy. A relevant research aspect of KIB is the development of a stable anode material that can efficiently cycle the large K + ions in its crystal structure within the 0 to 3 V potential window range; providing reasonable charge capacity and high reversibility. To this end, transition metal dichalcogenides or TMDs are promising electrode materials because of their favorable electrochemical properties. In this work, we study electrochemical performance of tungsten ditelluride (WTe 2 ) TMD as working electrode in a KIB half-cell. Results show that WTe 2 , a telluride-based TMD, has high first cycle specific charge capacity-with up to 3.3 K + stored per WTe 2 molecule (at least 4 times that of WS 2 electrode)-stable capacity of 143 mAh g −1 at 10th cycle number-outperforming WS 2 (66 mAh g −1 ) and graphite (95 mAh g −1 )-good reversibility, reasonable cycling stability, and low charge transfer resistance.