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The cycling stability of O3‐type NaNi1/3Fe1/3Mn1/3O2 (NFM) as a commercial cathode material for sodium ion batteries (SIBs) is still a challenge. In this study, the Ni/Fe/Mn elements are replaced successfully with tantalum (Ta) in the NFM lattice, which generated additional delocalized electrons and enhanced the binding ability between the transition metal and oxygen, resulting in suppressed lattice distortion during charging and discharging. This caused significant mitigation of voltage decay and improved cycle stability within the potential range of 2.0–4.2 V. The optimized Na(Ni1/3Fe1/3Mn1/3)0.97Ta0.03O2 sample achieved a reversible capacity of 162.6 mAh g−1 at a current rate of 0.1 C and 73.2 mAh g−1 at a high rate of 10 C. Additionally, the average charge/discharge potential retention reached 98% after 100 cycles, significantly mitigating the voltage decay. This work demonstrates a significant contribution towards the practical utilization of NFM cathodes in the SIBs energy storage field. [ABSTRACT FROM AUTHOR]

The practical application of sodium (Na) metal anode has been seriously hindered by the uncontrolled Na dendrite growth and severe volume expansion inducing short battery lifespan and safety concerns. Here, highly sodiophilic and ultrafine ZnS‐modified carbon fibers have been rationally constructed as a scaffold to obviate these drawbacks. The in situ generated Na2S‐reinforced fast ion transport interphase and the effective space confinement synergistically facilitate the fast sodium ion interfacial transfer and the homogeneous and dendrite‐free Na deposition, thus enabling high‐rate and dendrite‐free Na metal anode. The modified Na metal demonstrates ultrahigh rate capability (15 mA cm−2) and ultralong cycling life (5300 cycles). Moreover, the Na|Na3V2(PO4)3 (NVP) cell delivers ultrahigh rate capability (80 C) and extraordinarily ultralong lifespan cycling durability (2980 cycles). The Na|NVP pouch cell also exhibits an extraordinarily ultralong‐term cycle life of over 1070 cycles with an extremely low capacity decay rate of 0.0088% per cycle at 10 C. This work provides a facile and efficient strategy to propel the Na metal anode towards practicability. [ABSTRACT FROM AUTHOR]

The practical utilization of Li metal anodes has been significantly plagued by the challenges of uncontrollable dendritic Li growth and poor interphase instability. Here, the study reports a novel strategy to strengthen interphase and give highly efficient active seeds concurrently to stabilize Li metal via a highly lithiophilic In2O3 decorated porous scaffold. In situ configurated fast‐ion‐transport Li2O‐strengthened interphase layer cooperatively with highly efficient Li13In3 nucleation induction can endow the uniform Li nucleation/growth and high Li utilization efficiency. As a result, the achieved modified Li metal manifests high Coulombic efficiency, ultrahigh rate performance (5 mA cm−2), and ultra‐long lifespan cycling durability (7975 cycles). Importantly, the established Li|LiFePO4 cells exhibit long‐term cycling durability over 600 cycles at 1 C with an ultralow decay rate of ca. 0.017% per cycle. Moreover, the Li|LiCoO2 pouch cells with ultrahigh areal capacity of ca. 3.89 mAh cm−2 also exhibit extraordinarily prolonged cycling performance with excellent capacity retention despite extremely harsh cycling conditions of low negative‐to‐positive‐capacity (N/P) ratio of ca. 1.7 and lean electrolyte of ca. 4.9 g Ah−1. This work enlightens a facile and effective avenue toward highly stable Li metal anode toward reliable practicability. [ABSTRACT FROM AUTHOR]

Searching for novel solid electrolytes is of great importance and challenge for all‐solid‐state Mg batteries. In this work, we develop an amorphous Mg borohydride ammoniate, Mg(BH4)2·2NH3, as a solid Mg electrolyte that prepared by a NH3 redistribution between 3D framework‐γ‐Mg(BH4)2 and Mg(BH4)2·6NH3. Amorphous Mg(BH4)2·2NH3 exhibits a high Mg‐ion conductivity of 5 × 10−4 S cm−1 at 75 °C, which is attributed to the fast migration of abundant Mg vacancies according to the theoretical calculations. Moreover, amorphous Mg(BH4)2·2NH3 shows an apparent electrochemical stability window of 0–1.4 V with the help of in‐situ formed interphases, which can prevent further side reactions without hindering the Mg‐ion transfer. Based on the above superiorities, amorphous Mg(BH4)2·2NH3 enables the stable cycling of all‐solid‐state Mg cells, as the critical current density reaches 3.2 mA cm−2 for Mg symmetrical cells and the reversible specific capacity reaches 141 mAh g−1 with a coulombic efficiency of 91.7% (first cycle) for Mg||TiS2 cells. [ABSTRACT FROM AUTHOR]

Boosting the ultralow temperature (below −30 °C) performance of Na‐ion hybrid capacitors (SIHCs), which integrate the high energy density of batteries with the high output power and long life of supercapacitors, is critical for the application of advanced electronics in extreme environments. However, their low‐temperature performance, especially fast charging capability, is hindered by difficult desolvation and slow pass solid electrolyte interphase (SEI) together with sluggish diffusion within the electrode. Herein, a "single‐solute–single‐solvent" electrolyte is developed and a through‐hole hollow carbon sphere (TH‐HCS) is constructed, and it is demonstrated through theoretical calculations and experimental investigations that the weakly solvated structure and high ionic conductivity facilitate the Na+ transportation at low temperatures, the highly fluorinated SEI facilitates the Na+ migration, and the through‐hole hollow structure alleviates the volume expansion during sodiation, thus ensuring fast kinetics and structural stability. As expected, TH‐HCS using this electrolyte exhibits a high specific capacity of 87.5 mAh g−1 after 11 000 cycles at 1.0 A g−1 and −40 °C. Coupled with activated carbon, the assembled SIHC displays an energy density of 106.1 and 52.0 Wh kg−1 at 25 and −40 °C, respectively, far exceeding the performance of commercial energy storage systems at low temperature. [ABSTRACT FROM AUTHOR]

A new Fe-substituted TiFeNb10O29−δ (TFNO) anode is proposed. TFNO possesses a defective and polycrystalline ReO3 Roth–Wadsley shear structure with a slightly larger lattice volume. Electrochemical behavior results and density functional theory (DFT) calculations show that TFNO can facilitate the kinetics of electron/Li+ transportation and demonstrates pseudocapacitive behavior. Consequently, TFNO exhibits superior high rate capacity and cycling stability compared to pristine TNO, offering 100 mA h g−1 at an ultrahigh rate of 50C and a high capacity retention of 86.7% over 1000 cycles at 10C. This work reveals that TFNO could be a promising anode material for fast-charging, stable, and safe LIBs. [ABSTRACT FROM AUTHOR]