Search

Although Mg–Li dual metal-ion batteries are proposed as a superior system that unite safety of Mg-batteries and performance of Li-ion based systems, its practical implantation is limited due to the lack of reliable high-performance cathodes. Herein, we report a high-performance Mg–Li dual metal-ion battery system based on highly pseudocapacitive hierarchical TiO2-B nanosheet assembled spheres (NS) cathode. This 2D cathode displayed exceptional pseudocapacitance (a maximum of 93%) specific capacity (303 mAh g −1 at 25 mA g−1), rate performance (210 mAh g −1 at 1 A g−1), consistent cycling (retain ∼100% capacity for 3000 cycles at 1 A g−1), Coulombic efficiency (nearly 100%) and fast-charging (∼12.1 min). These properties are remarkably dominant to the existing Mg-Li dual metal-ion battery cathodes. Spectroscopic and microscopic mechanistic studies confirmed negligible structural changes during charge-discharge cycles of the TiO2-B nanosheet assembled spheres electrodes. Exceptional electrochemical properties of the 2D electrode is ascribed to remarkable pseudocapacitive Mg–Li dual metal-ion diffusion via the numerous nanointerfaces of TiO2-B caused by its hierarchical microstrucrure. Large surface area, nanosheet morphology, mesoporous structure and ultrathin nature also acted as secondary factors facilitating improved electrode-electrolyte contact. Demonstrated approach of pseudocapacitive type Mg-Li dual metal-ion intercalation through hierarchical nanointerfaces may be further utilized for the designing of numerous top-notch electrode materials for futuristic Mg–Li dual metal-ion batteries. [ABSTRACT FROM AUTHOR]

Disordered carbon is the state of the art anode material for Na‐ion batteries due to their increased interlayer spacing and good electronic conductivity. However, its practical application is hindered by average specific capacity, poor rate performance, low coulombic efficiency and limited cycling stability. Herein, we report the superior pseudocapacitance enhanced Na‐ion storage of in situ surface functionalized carbon nanosheets. Anodes composed of ultrathin (~15 nm) carbon nanosheets demonstrated excellent reversible specific capacity (375 mAh/g at 25 mA/g), rate performance (150 mAh/g at 2 A/g), long‐term cycling performance (1000 cycles at 1 A/g) and coulombic efficiency (~100 %). Considerably higher pseudocapacitance (up to ~78 %) is also identified in this case compared to amorphous carbon particles. Spectroscopic and electrochemical studies proved Na‐ion intercalation in to the disordered carbon and pseudocapacitive storage driven by oxygen‐containing surface functional groups. Outstanding electrochemical performance is credited to the synergy between diffusion limited intercalation and pseudocapacitive surface Na‐ion storage. The demonstrated synthetic method of in situ functionalized carbon nanosheets is inexpensive and scalable. The strategy of functional group and morphology induced pseudocapacitive Na‐ion storage offer new prospects to design high‐performance Na‐ion battery electrodes. [ABSTRACT FROM AUTHOR]

Secondary lithium-ion batteries are restricted in large-scale applications including power grids and long driving electric vehicles owing to the low specific capacity of conventional intercalation anodes possessing sluggish Li-ion diffusion kinetics. Herein, we demonstrate an unusual pseudocapacitive lithium-ion storage on defective Co3O4 nanosheet anodes for high-performance rechargeable batteries. Cobalt-oxide nanosheets presented here composed of various defects including vacancies, dislocations and grain boundaries. Unique 2D holey microstructure enabled efficient charge transport as well as provided room for volume expansions associated with lithiation-delithiation process. These defective anodes exhibited outstanding pseudocapacitance (up to 87%), reversible capacities (1490 mAh gâ€"1 @ 25 mA gâ€"1), rate capability (592 mAh gâ€"1 @ 30 A gâ€"1), stable cycling (85% after 500 cycles @ 1 A gâ€"1) and columbic efficiency (∼100%). Exceptional Li-ion storage phenomena in defective Co3O4 nanosheets is accredited to the pseudocapacitive nature of conversion reaction resulting from ultrafast Li-ion diffusion through various crystal defects. The demonstrated approach of defect-induced pseudocapacitance can also be protracted for various low-cost and/or eco-friendly transition metal-oxides for next-generation rechargeable batteries. [ABSTRACT FROM AUTHOR]

Despite the proposed safety, performance, and cost advantages, practical implementation of Mg−Li hybrid batteries is limited due to the unavailability of reliable cathodes compatible with the dual‐ion system. Herein, a high‐performance Mg−Li dual ion battery based upon cobalt‐doped TiO2 cathode was developed. Extremely pseudocapacitance‐type Ti1‐xCoxO2‐y nanosheets consist of an optimum 3.57 % Co‐atoms. This defective cathode delivered exceptional pseudocapacitance (maximum of 93 %), specific capacities (386 mAh g−1 at 25 mA g−1), rate performance (191 mAh g−1 at 1 A g−1), cyclability (3000 cycles at 1 A g−1), and coulombic efficiency (≈100 %) and fast charging (≈11 min). This performance was superior to the TiO2‐based Mg−Li dual‐ion battery cathodes reported earlier. Mechanistic studies revealed dual‐ion intercalation pseudocapacitance with negligible structural changes. Excellent electrochemical performance of the cation‐doped TiO2 cathode was credited to the rapid pseudocapacitance‐type Mg/Li‐ion diffusion through the disorder generated by lattice distortions and oxygen vacancies. Ultrathin nature, large surface area, 2D morphology, and mesoporosity also contributed as secondary factors facilitating superior electrode‐electrolyte interfacial kinetics. The demonstrated method of pseudocapacitance‐type Mg−Li dual‐ion intercalation by introducing lattice distortions/oxygen vacancies through selective doping can be utilized for the development of several other potential electrodes for high‐performance Mg−Li dual‐ion batteries. [ABSTRACT FROM AUTHOR]

High-performance anodes for rechargeable Li-ion batteries are produced by nanostructuring of transition metal oxides on a conductive support. Here, we demonstrate a hybrid material of MnO2 directly grown onto fabrics of carbon nanotube fibres, which exhibits notable specific capacities over 1100 and 500 mA h g−1 at discharge current densities of 25 mA g−1 and 5 A g−1, respectively, with a coulombic efficiency of 97.5%. Combined with 97% capacity retention after 1500 cycles at a current density of 5 A g−1, both capacity and stability are significantly above literature data. Detailed investigations involving electrochemical and in situ synchrotron X-ray scattering studies reveal that during galvanostatic cycling, MnO2 undergoes an irreversible phase transition to LiMnO2, which stores lithium through an intercalation process, followed by a conversion mechanism and pseudocapacitive processes. This mechanism is further confirmed by Raman spectroscopy and X-ray photoelectron spectroscopy. The fraction of pseudocapacitive charge storage ranges from 27% to 83%, for current densities from 25 mA g−1 to 5 A g−1. The firm attachment of the active material to the built-in current collector makes the electrodes flexible and mechanically robust, and ensures that the low charge transfer resistance and the high electrode surface area remain after irreversible phase transition of the active material and extensive cycling. [ABSTRACT FROM AUTHOR]