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• The partial S-doping NiFe 2 O 4 was obtained through a facile hydrothermal method. • The d-spacing of NiFe 2 O 4 was expended caused by partial S-doping. • The impact of partial S-doping to NiFe 2 O 4 is exposed by VASP analysis. • The optimal electrode exhibited the highest specific capacitance of 284 F/g. Nickel ferrite exhibits many advantages as electrode materials in the application of supercapacitor, such as high energy capacity and excellent cycle stability. Whereas, compared with identical-metal sulfides, the specific capacitance of NiFe 2 O 4 is still insufficient. Hence, to combine the superiorities of oxides and sulfides, partial sulfur doping NiFe 2 O 4 is obtained through hydrothermal synthesis method. Analyzed by Vienna Ab-initio Simulation Package (VASP) software and high-resolution transmission electron microscopy, the lattice parameters of NiFe 2 O 4 are confirmed to be expanded by introducing sulfur atoms, which is beneficial to electrochemical performances. At a current density of 1 A/g, the specific capacitance of partial sulfur doping NiFe 2 O 4 is calculated to be 284 F/g, higher than that of the original NiFe 2 O 4 of 182.2 F/g. Moreover, a maximum energy density of 21.14 Wh/kg is achieved at a power density of 375 W/kg. This work shows that partial sulfur doping could improve the electrochemical performance of NiFe 2 O 4. To sum up, this work provides an effective way to enhance the poor electrochemical performance of oxides, greatly encouraging the application of oxides in energy storage field. [Display omitted] [ABSTRACT FROM AUTHOR]

Morphology of transition metal oxide largely affects its electrochemical energy storage properties. This also applies to its composites. In this paper, NiFe 2 O 4 /Graphene nanosheets composites (NFO/GNSs) are successfully prepared by a facile hydrothermal method. NiFe 2 O 4 (NFO) in the sample exhibits a unique nanosheet morphology, vertically arranging on the graphene nanosheets (GNSs). Microscopically, NFO nanosheets interpenetrate on the surface of graphene to form a continuous network structure. The sample exhibits excellent specific capacitance and rate performance. It is worth mentioning that the specific capacitance increases to 140% after 5000 cycles, showing superior cycle stability. This may be due to the conductive network formed by NFO nanosheets and GNSs. Excellent electrochemical performance indicates excellent application prospects of materials in supercapacitor electrodes. Image 1 • Unique NiFe 2 O 4 nanosheets structure with graphene nanosheets was successfully prepared by a hydrothermal method. • NiFe 2 O 4 nanosheets/graphene performed a better specific capacitance, arriving at 464.15 F/g at current density of 1 A/g. • The network structure formed between NiFe 2 O 4 nanosheets and graphene nanosheets provides excellent cycle performance. [ABSTRACT FROM AUTHOR]

The new inorganic material known as "high-entropy oxides" (HEOs) has a single-phase structure and is made up of several different main metal elements. It has many useful properties, including a high specific capacity, excellent cycling performance, high structural stability, and super-electronic conductivity. For lithium-ion batteries, it is viewed as a promising electrode material (LIBs). It is significant to develop high entropy oxides with different components and study their properties. Herein, Mg, Ni and Li are added to the quaternary medium entropy (CrFeMnCo)3O4. Four new spinel high entropy oxides were synthesized by glycine-nitrate SCS method at 750 °C and their material characterization and electrochemical properties were investigated respectively. The experimental results show that the four obtained samples have uniform particle size distribution. As for the electrochemical test, the capacities of the (CrFeMnCoMg)3O4 and (CrFeMnCoNi)3O4 do not decrease significantly after 800 cycles at 2000 mA·g−1. They have better cycle stability than the (CrFeMnCoMgLi)3O4 and (CrFeMnCoNiLi)3O4. As the anode of LIBs, all HEOs show excellent cycle stability and rate capability. This work provides a new strategy for designing high-entropy energy storage materials. [ABSTRACT FROM AUTHOR]

The layered transition metal oxides are an essential class of cathode materials in sodium-ion batteries. However, the capacity decay mechanisms of many materials at a wide voltage window are still ambiguous. Therefore, research on the intrinsic structure of materials at the electronic or atomic level is of great significance to unlock the potential of more materials. In this study, a new family of layered NaNi 0.45 Mn 0.3 Ti 0.2 M 0.05 O 2 (M = Nb/Mo/Cr) has been demonstrated to combine high specific capacity (NaNi 0.45 Mn 0.3 Ti 0.2 Cr 0.05 O 2 , 12 mA g−1, 185.7 mAh g−1, 2-4.2 V) with preferable Na+ insertion/extraction activity (1920 mA g−1, 111.2 mAh g−1). The participation of Ni2+/Ni3+ and Cr3+/Cr4+/Cr6+ in the redox reaction upon cycling significantly contributes to the superior specific capacity, and the diffusion kinetics calculation indicates that the substitution of Cr for Ni can create a more suitable path with a low energy barrier for Na+ movement, which is particularly crucial for the rate performance. Besides, the unfavorable cycling stability is affected by the distortion of the crystal structure, suggesting that the Jahn-Teller effect of Mn3+/Ni3+ and the second-order Jahn-Teller effect of Nb5+/Mo6+ (d0 transition metal) together with Cr6+ migration caused by disproportionation of Cr4+ have inescapable responsibilities. Additionally, the reversible phase transition between the O3 and P3 phases upon Na+ insertion/extraction at a wide voltage window is identified by in situ XRD measurements and verified to be the key factor of the high coulombic efficiency for NMTCr. An in-depth understanding of NMTNb and NMTMo can provide new insights for material design and exploitation. The composition-structure-property relationships behind the electrochemical performance can be comprehended profoundly by coupling the experimental verification with density functional theory calculations. • A new family of layered NaNi 0.45 Mn 0.3 Ti 0.2 M 0.05 O 2 (M = Nb/Mo/Cr) has been prepared. • The participation of Ni2+/Ni3+ and Cr3+/Cr4+/Cr6+ contributes greatly to the capacity. • The substitution of Cr provided a suitable path with low energy barrier for Na+ movement. • The Jahn-Teller effect of Mn3+/Ni3+ and second-order JT effect of Nb5+/Mo6+ are discussed. [ABSTRACT FROM AUTHOR]