Activating Selenium Cathode Chemistry for Aqueous Zinc-Ion Batteries.

Aqueous rechargeable zinc-ion batteries (ARZIBs) are a promising next-generation energy-storage device by virtue of the superior safety and low cost of both the aqueous electrolyte and zinc-metal anode. However, their development is hindered by the lack of suitable cathodes with high volumetric capacity that can provide both lightweight and compact size. Herein, a novel cathode chemistry based on amorphous Se doped with transition metal Ru that mitigates the resistive surface layer produced by the side reactions between the Se cathode and aqueous electrolyte is reported. This improvement can permit high volumetric capacity in this system. Distinct from the conventional conversion mechanisms between Se and ZnSe in Se||Zn cells, this strategy realizes synchronous proton and Zn2+ intercalation/deintercalation in the Ru-doped amorphous Se||Zn half cells. Moreover, an unanticipated Zn2+ deposition/stripping process in this system further contributes to the superior electrochemical performance of this new cathode chemistry. Consequently, the Ru-doped amorphous Se||Zn half cells are found to deliver a record-high capacity of 721 mAh g-1 /3472 mAh cm-3 , and superior cycling stability of over 800 cycles with only 0.015% capacity decay per cycle. This reported work opens the door for new chemistries that can further improve the gravimetric and volumetric capacity of ARZIBs.

High-Entropy Solid-State Na-Ion Conductor for Stable Sodium-Metal Batteries.

Solid-state sodium-metal batteries (SSBs) hold great promise for their merits in low-cost, high energy density, and safety. However, developing solid electrolyte (SE) materials for SSBs with high performance is still a great challenge. In this study, high-entropy Na4.9 Sm0.3 Y0.2 Gd0.2 La0.1 Al0.1 Zr0.1 Si4 O12 was synthesized at comparatively low sintering temperature of 950 °C with high room-temperature ionic conductivity of 6.7×10-4  S cm-1 and a low activation energy of 0.22 eV. More importantly, the Na symmetric cells using high-entropy SE show a high critical current density of 0.6 mA cm-2 , outstanding rate performance with fairly flat potential profiles at 0.5 mA cm-2 and steady cycling over 700 h under 0.1 mA cm-2 . Solid-state Na3 V2 (PO4 )3 ||high-entropy SE||Na batteries are further assembled manifesting a desirable cycling stability with almost no capacity decay after 600 cycles and high Columbic efficiency over 99.9 %. The findings present opportunities for the design of high-entropy Na-ion conductors toward the development of SSBs.

Joint Enhancement in the Electrochemical Reversibility and Cycle Lives for Copper Sulfide for Sodium- and Potassium-Ion Storage via Selenium Substitution.

Transition metal sulfides have received considerable interest as the anodes for sodium-ion (SIBs) and potassium-ion batteries (PIBs) owing to their high theoretical capacity and suitable working potential. However, they suffer from poor electrochemical reversibility and limited cycle lives. Herein, we design and synthesize a Se-substituted CuS material, which demonstrates superior electrochemical properties for both potassium and sodium storage because of the enhanced electronic conductivity, lowered diffusion barrier, and shortened diffusion pathway. The anode delivers a specific capacity of 374 mA h g-1 at a current density of 5 A g-1 in SIBs and 341 mA h g-1 at 2 A g-1 in PIBs and nearly 100% capacity retention over 2000 cycles (SIBs) and 600 cycles (PIBs), respectively. Moreover, a combined measurement including X-ray diffraction, Raman, and transmission electron microscopy reveals an interesting discharge product of Na2S0.8Se0.2, which could accelerate the conversion reaction and enhance the electrochemical reversibility.

Boosting potassium-storage performance via the functional design of a heterostructured Bi2S3@RGO composite.

Potassium-ion batteries (PIBs) are considered a promising alternative to lithium-ion batteries (LIBs) for next-generation energy storage due to the abundance and competitive cost of potassium resources. However, the excavation and the development of proper electrodes for PIBs are still confronted with great challenges. Herein, a self-assembled bismuth sulfide microsphere wrapped with reduced graphene oxide was fabricated to form a heterostructured Bi2S3@RGO composite via a visible-light-assisted method and served as the anode for PIBs. The as-prepared Bi2S3@RGO composite presented a high reversible specific capacity of 538 mA h g-1 at 0.2 A g-1 and superior rate capability of 237 mA h g-1 at a high current density of 2 A g-1 after 300 cycles. In particular, the high capacity could be ascribed to the synergistic effect of the conversion and alloying reactions during the electrochemical processes, which was validated by ex situ X-ray diffraction. The fabrication of a unique heterostructure combining the self-assembled Bi2S3 microspheres and flexible RGO boosted the facile charge transfer, leading to the enhanced cyclic stability and rate performance.