Shuangshuang Tan

Porous One‐Dimensional Nanomaterials: Design, Fabrication and Applications in Electrochemical Energy Storage

Electrochemical energy storage technology is of critical importance for portable electronics, transportation and large-scale energy storage systems. There is a growing demand for energy storage devices with high energy and high power densities, long-term stability, safety and low cost. To achieve these requirements, novel design structures and high performance electrode materials are needed. Porous 1D nanomaterials which combine the advantages of 1D nanoarchitectures and porous structures have had a significant impact in the field of electrochemical energy storage. This review presents an overview of porous 1D nanostructure research, from the synthesis by bottom-up and top-down approaches with rational and controllable structures, to several important electrochemical energy storage applications including lithium-ion batteries, sodium-ion batteries, lithium-sulfur batteries, lithium-oxygen batteries and supercapacitors. Highlights of porous 1D nanostructures are described throughout the review and directions for future research in the field are discussed at the end.

Pseudocapacitive titanium oxynitride mesoporous nanowires with iso-oriented nanocrystals for ultrahigh-rate sodium ion hybrid capacitors

Titanium oxynitride mesoporous nanowires (Ti(O,N)-MP-NWs) composed of iso-oriented interconnected nanocrystals with [100] preferred orientation and tunable O/N ratios are synthesized, based on an anion exchange process. By investigating the electrochemical performance, it is found to exhibit high pseudocapacitive sodium storage performance, demonstrated by kinetic analysis and experimental characterizations. Subsequently, the assembled asymmetric hybrid sodium ion capacitor (AC//Ti(O,N)) exhibits high energy and power densities. Our work proposes the high pseudocapacitance in non-aqueous sodium ion system is very promising for high-power and low-cost energy storage applications.

VO2 Nanoflakes as the Cathode Material of Hybrid Magnesium–Lithium-Ion Batteries with High Energy Density

The hybrid magnesium-lithium-ion batteries (MLIBs) combining the dendrite-free deposition of the Mg anode and the fast Li intercalation cathode are better alternatives to Li-ion batteries (LIBs) in large-scale power storage systems. In this article, we reported hybrid MLIBs assembled with the VO2 cathode, dendrite-free Mg anode, and the Mg-Li dual-salt electrolyte. Satisfactorily, the VO2 cathode delivered a stable plateau at about 1.75 V, and a high specific discharge capacity of 244.4 mA h g-1. To the best of our knowledge, the VO2 cathode displays the highest energy density of 427 Wh kg-1 among reported MLIBs in coin-type batteries. In addition, an excellent rate performance and a wide operating temperature window from 0 to 55 °C have been obtained. The combination of VO2 cathode, dual-salt electrolyte, and Mg anode would pave the way for the development of high energy density, safe, and low-cost batteries.

H2V3O8 Nanowires as High-Capacity Cathode Materials for Magnesium-Based Battery

Magnesium-based batteries have received much attention as promising candidates to next-generation batteries because of high volumetric capacity, low price, and dendrite-free property of Mg metal. Herein, we reported H2V3O8 nanowire cathode with excellent electrochemical property in magnesium-based batteries. First, it shows a satisfactory magnesium storage ability with 304.2 mA h g-1 capacity at 50 mA g-1. Second, it possesses a high-voltage platform of ∼2.0 V vs Mg/Mg2+. Furthermore, when evaluated as a cathode material for magnesium-based hybrid Mg2+/Li+ battery, it exhibits a high specific capacity of 305.4 mA h g-1 at 25 mA g-1 and can be performed in a wide working temperature range (-20 to 55 °C). Notably, the insertion-type ion storage mechanism of H2V3O8 nanowires in hybrid Mg2+/Li+ batteries are investigated by ex situ X-ray diffraction and Fourier transform infrared. This research demonstrates that the H2V3O8 nanowire cathode is a potential candidate for high-performance magnesium-based batteries.

Multidimensional Synergistic Nanoarchitecture Exhibiting Highly Stable and Ultrafast Sodium‐Ion Storage

Conversion-type anodes with multielectron reactions are beneficial for achieving a high capacity in sodium-ion batteries. Enhancing the electron/ion conductivity and structural stability are two key challenges in the development of high-performance sodium storage. Herein, a novel multidimensionally assembled nanoarchitecture is presented, which consists of V2 O3 nanoparticles embedded in amorphous carbon nanotubes that are then coassembled within a reduced graphene oxide (rGO) network, this materials is denoted V2 O3 ⊂C-NTs⊂rGO. The selective insertion and multiphase conversion mechanism of V2 O3 in sodium-ion storage is systematically demonstrated for the first time. Importantly, the naturally integrated advantages of each subunit synergistically provide a robust structure and rapid electron/ion transport, as confirmed by in situ and ex situ transmission electron microscopy experiments and kinetic analysis. Benefiting from the synergistic effects, the V2 O3 ⊂C-NTs⊂rGO anode delivers an ultralong cycle life (72.3% at 5 A g-1 after 15 000 cycles) and an ultrahigh rate capability (165 mAh g-1 at 20 A g-1 , ≈30 s per charge/discharge). The synergistic design of the multidimensionally assembled nanoarchitecture produces superior advantages in energy storage.

High-Performance Na–O2 Batteries Enabled by Oriented NaO2 Nanowires as Discharge Products

Na-O2 batteries are emerging rechargeable batteries due to their high theoretical energy density and abundant resources, but they suffer from sluggish kinetics due to the formation of large-size discharge products with cubic or irregular particle shapes. Here, we report the unique growth of discharge products of NaO2 nanowires inside Na-O2 batteries that significantly boosts the performance of Na-O2 batteries. For this purpose, a high-spin Co3O4 electrocatalyst was synthesized via the high-temperature oxidation of pure cobalt nanoparticles in an external magnetic field. The discharge products of NaO2 nanowires are 10-20 nm in diameter and ∼10 μm in length, characteristics that provide facile pathways for electron and ion transfer. With these nanowires, Na-O2 batteries have surpassed 400 cycles with a fixed capacity of 1000 mA h g-1, an ultra-low over-potential of ∼60 mV during charging, and near-zero over-potential during discharging. This strategy not only provides a unique way to control the morphology of discharge products to achieve high-performance Na-O2 batteries but also opens up the opportunity to explore growing nanowires in novel conditions.

Pseudocapacitive layered birnessite sodium manganese dioxide for high-rate non-aqueous sodium ion capacitors

Layered transition metal oxides are promising cathodes for sodium ion capacitors due to their high specific capacity. In this work, we present a layered birnessite sodium manganese dioxide (Na0.77MnO2·0.5H2O) supported by a two-dimensional conductive network (denoted as b-NMO/C) as a cathode for non-aqueous sodium ion capacitor (SIC). The interlayer crystal water and carbon networks promote the ion/electron transport kinetics and overcome the structural instability, leading to largely enhanced electrochemical performance. As a result, the as-synthesized b-NMO/C cathode delivers a capacity of 192 mA h g−1 at 0.25C and 43 mA h g−1 even at a high rate of 100C. The attained performance is compared favorably with those of state-of-the-art Mn-based cathodes for sodium ion storage. Furthermore, the assembled asymmetric SIC (b-NMO/C//graphite) exhibits the highest energy (91 W h kg−1 achieved at ∼84 W kg−1) and power (5816 W kg−1 achieved at ∼37 W h kg−1) densities within the voltage range of 0.5–3.8 V.

Interlayer-Spacing-Regulated VOPO4 Nanosheets with Fast Kinetics for High-Capacity and Durable Rechargeable Magnesium Batteries

Owing to the low-cost, safety, dendrite-free formation, and two-electron redox properties of magnesium (Mg), rechargeable Mg batteries are considered as promising next-generation secondary batteries with high specific capacity and energy density. However, the clumsy Mg2+ with high polarity inclines to sluggish Mg insertion/deinsertion, leading to inadequate reversible capacity and rate performance. Herein, 2D VOPO4 nanosheets with expanded interlayer spacing (1.42 nm) are prepared and applied in rechargeable magnesium batteries for the first time. The interlayer expansion provides enough diffusion space for fast kinetics of MgCl+ ion flux with low polarization. Benefiting from the structural configuration, the Mg battery exhibits a remarkable reversible capacity of 310 mAh g-1 at 50 mA g-1 , excellent rate capability, and good cycling stability (192 mAh g-1 at 100 mA g-1 even after 500 cycles). In addition, density functional theory (DFT) computations are conducted to understand the electrode behavior with decreased MgCl+ migration energy barrier compared with Mg2+ . This approach, based on the regulation of interlayer distance to control cation insertion, represents a promising guideline for electrode material design on the development of advanced secondary multivalent-ion batteries.

Sodium Ion Capacitor Using Pseudocapacitive Layered Ferric Vanadate Nanosheets Cathode

Summary Sodium ion capacitors (SICs) are designed to deliver both high energy and power densities at low cost. Electric double-layer capacitive cathodes are typically used in these devices, but they lead to very limited capacity. Herein, we apply a pseudocapacitive layered ferric vanadate (Fe-V-O) as cathode to construct non-aqueous SICs with both high energy and power densities. The Fe-V-O nanosheets cathode displays remarkable rate capability and cycling stability. The pseudocapacitive sodium storage mechanism of Fe-V-O, with over 83% of total capacity from capacitive contribution, is confirmed by kinetics analysis and ex situ characterizations. The capacitive-adsorption mechanism of hard carbon (HC) anode is demonstrated, and it delivers excellent rate capability. Based on as-synthesized materials, the assembled HC//Fe-V-O SIC delivers a maximum energy density of 194 Wh kg−1 and power density of 3,942 W kg−1. Our work highlights the advantages of pseudocapacitive cathodes for achieving both high energy and power densities in sodium storage devices.

Amine-assisted synthesis of FeS@N-C porous nanowires for highly reversible lithium storage

Iron sulfide is an attractive anode material for lithium-ion batteries (LIBs) due to its high specific capacity, environmental benignity, and abundant resources. However, its application is hindered by poor cyclability and rate performance, caused by a large volume variation and low conductivity. Herein, iron sulfide porous nanowires confined in an N-doped carbon matrix (FeS@N-C nanowires) are fabricated through a simple amine-assisted solvothermal reaction and subsequent calcination strategy. The as-obtained FeS@N-C nanowires, as an LIB anode, exhibit ultrahigh reversible capacity, superior rate capability, and long-term cycling performance. In particular, a high specific capacity of 1,061 mAh·g−1 can be achieved at 1 A·g−1 after 500 cycles. Most impressively, it exhibits a high specific capacity of 433 mAh·g−1 even at 5 A·g−1. The superior electrochemical performance is ascribed to the synergistic effect of the porous nanowire structure and the conductive N-doped carbon matrix. These results demonstrate that the synergistic strategy of combining porous nanowires with an N-doped carbon matrix holds great potential for energy storage.