Sonochemistry-enabled uniform coupling of SnO2 nanocrystals with graphene sheets as anode materials for lithium-ion batteries

SnO₂/graphene nanocomposite was successfully synthesized by a facile sonochemical method from SnCl₂ and graphene oxide (GO) precursors. In the sonochemical process, the Sn²⁺ is firstly dispersed homogeneously on the GO surface, then in situ oxidized to SnO₂ nanoparticles on both sides of the graphene nanosheets (RGO) obtained by the reduction of GO under continuous ultrasonication. Graphene not only provides a mechanical support to alleviate the volume changes of the SnO₂ anode and prevent nanoparticle agglomeration, but also serves as a conductive network to facilitate charge transfer and Li⁺ diffusion. When used as a lithium ion battery (LIB) anode, the SnO₂/graphene nanocomposite exhibits significantly improved specific capacity (1610 mA h g⁻¹ at 100 mA g⁻¹), good cycling stability (retaining 87% after 100 cycles), and competitive rate performance (273 mA h g⁻¹ at 500 mA g⁻¹) compared to those of bare SnO₂. This sonochemical method can be also applied to the synthesis of other metal-oxide/graphene composites and this work provides a large-scale preparation route for the practical application of SnO₂ in lithium ion batteries.

SnO₂/graphene nanocomposite was successfully synthesized by a facile sonochemical method from SnCl₂ and graphene oxide (GO) precursors.     

Design and synthesis of graphene/SnO2/polyacrylamide nanocomposites as anode material for lithium-ion batteries

Tin dioxide (SnO₂) is a promising anode material for lithium-ion batteries owing to its large theoretical capacity (1494 mA h g⁻¹). However, its practical application is hindered by these problems: the low conductivity, which restricts rate performance of the electrode, and the drastic volume change (400%). In this study, we designed a novel polyacrylamide/SnO₂ nanocrystals/graphene gel (PAAm@SnO₂NC@GG) structure, in which SnO₂ nanocrystals anchored in three-dimensional graphene gel network and the polyacrylamide layers could effectively prevent the agglomeration of SnO₂ nanocrystals, presenting excellent cyclability and rate performance. A capacity retention of over 90% after 300 cycles of 376 mA h g⁻¹ was achieved at a current density of 5 A g⁻¹. In addition, a stable capacity of about 989 mA h g⁻¹ at lower current density of 0.2 A g⁻¹ was achieved.

Tin dioxide (SnO₂) is a promising anode material for lithium-ion batteries owing to its large theoretical capacity (1494 mA h g⁻¹).     

Porous SnO2 nanostructure with a high specific surface area for improved electrochemical performance

Tin oxide (SnO₂) has been attractive as an alternative to carbon-based anode materials because of its fairly high theoretical capacity during cycling. However, SnO₂ has critical drawbacks, such as poor cycle stability caused by a large volumetric variation during the alloying/de-alloying reaction and low capacity at a high current density due to its low electrical conductivity. In this study, we synthesized a porous SnO₂ nanostructure (n-SnO₂) that has a high specific surface area as an anode active material using the Adams fusion method. From the Brunauer–Emmett–Teller analysis and transmission electron microscopy, the as-prepared SnO₂ sample was found to have a mesoporous structure with a fairly high surface area of 122 m² g⁻¹ consisting of highly-crystalline nanoparticles with an average particle size of 5.5 nm. Compared to a commercial SnO₂, n-SnO₂ showed significantly improved electrochemical performance because of its increased specific surface area and short Li⁺ ion pathway. Furthermore, during 50 cycles at a high current density of 800 mA g⁻¹, n-SnO₂ exhibited a high initial capacity of 1024 mA h g⁻¹ and enhanced retention of 53.6% compared to c-SnO₂ (496 mA h g⁻¹ and 23.5%).

A porous SnO₂ nanostructure as an anode active material showed significantly improved electrochemical performance.     

Crystal-seeds induced construction of ZnO–ZnFe2O4 micro-cubic composites as excellent anode materials for lithium ion battery

This work aims at designing a fine assembly of two different transition metal oxides with a distinct band-gap energy into a bi-component-active hetero-structure to enhance the hetero-interface interactions and synergetic functionalities of bi-components to improve electrochemical performance. Herein, a facile marriage of crystal-seeds induction and hydrothermal reactions has been utilized to fabricate ZnO–ZnFe₂O₄ micro-cubic composites. Benefiting from the synergetic effects of the bi-functional components and their unique hetero-junction structure, the ZnO–ZnFe₂O₄ micro-cubic composites exhibit a significant improvement in lithium storage performance. The reversible capacity is retained at a value of 811 mA h g⁻¹ after 200 cycles at a current density of 100 mA g⁻¹. Even at high current densities of 1 and 5 A g⁻¹, the electrodes are still able to deliver capacities of 584 and 430 mA h g⁻¹ after 200 cycles, respectively.

This work aims at designing a fine assembly of two different transition metal oxides with a distinct band-gap energy into a bi-component-active hetero-structure to improve electrochemical performance.     

Highly crystalline nickel hexacyanoferrate as a long-life cathode material for sodium-ion batteries

Prussian blue analogs (PBAs) are attractive cathode candidates for high energy density, including long life-cycle rechargeable batteries, due to their non-toxicity, facile synthesis techniques and low cost. Nevertheless, traditionally synthesized PBAs tend to have a flawed crystal structure with a large amount of [Fe(CN)₆]⁴⁻ openings and the presence of crystal water in the framework; therefore the specific capacity achieved has continuously been low with poor cycling stability. Herein, we demonstrate low-defect and sodium-enriched nickel hexacyanoferrate nanocrystals synthesized by a facile low-speed co-precipitation technique assisted by a chelating agent to overcome these problems. As a consequence, the prepared high-quality nickel hexacyanoferrate (HQ-NiHCF) exhibited a high specific capacity of 80 mA h g⁻¹ at 15 mA g⁻¹ (with a theoretical capacity of ∼85 mA h g⁻¹), maintaining a notable cycling stability (78 mA h g⁻¹ at 170 mA g⁻¹ current density) without noticeable fading in capacity retention after 1200 cycles. This low-speed synthesis strategy for PBA-based electrode materials could be also extended to other energy storage materials to fabricate high-performance rechargeable batteries.

A low-speed synthesis strategy was designed to fabricate Prussian blue analog based electrode materials for high-performance rechargeable batteries.     

A nanostructured SnO2/Ni/CNT composite as an anode for Li ion batteries

A SnO₂/Ni/CNT nanocomposite was synthesized using a simple one-step hydrothermal method followed by calcination. A structural study via XRD shows that the tetragonal rutile structure of SnO₂ is maintained. Further, X-ray photoelectron spectroscopy (XPS) and Raman studies confirm the existence of SnO₂ along with CNTs and Ni nanoparticles. The electrochemical performance was investigated via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge–discharge measurements. The nanocomposite has been used as an anode material for lithium-ion batteries. The SnO₂/Ni/CNT nanocomposite exhibited an initial discharge capacity of 5312 mA h g⁻¹ and a corresponding charge capacity of 2267 mA h g⁻¹ during the first cycle at 50 mA g⁻¹. Pristine SnO₂ showed a discharge/charge capacity of 1445/636 mA h g⁻¹ during the first cycle at 50 mA g⁻¹. This clearly shows the effects of the optimum concentrations of CNTs and Ni. Further, the nanocomposite (SnNiCn) shows a discharge capacity as high as 919 mA h g⁻¹ after 210 cycles at a current density of 400 mA g⁻¹ in a Li-ion battery set-up. Thus, the obtained capacity from the nanocomposite is much higher compared to pristine SnO₂. The higher capacity in the nanoheterostructure is due to the well-dispersed nanosized Ni-decorated stabilized SnO₂ along with the CNTs, avoiding pulverization as a result of the volumetric change of the nanoparticles being minimized. The material accommodates huge volume expansion and avoids the agglomeration of nanoparticles during the lithiation and delithiation processes. The Ni nanoparticles can successfully inhibit Sn coarsening during cycling, resulting in the enhancement of stability during reversible conversion reactions. They ultimately enhance the capacity, giving stability to the nanocomposite and improving performance. Additionally, the material exhibits a lower Warburg coefficient and higher Li ion diffusion coefficient, which in turn accelerate the interfacial charge transfer process; this is also responsible for the enhanced stable electrochemical performance. A detailed mechanism is expressed and elaborated on to provide a better understanding of the enhanced electrochemical performance.

SnO₂/Ni/CNT nanocomposite approach has been demonstrated which confers shielding against volume expansion due to the use of optimum % of Ni & CNT exhibiting superior cycling stability and rate capabilities of the stable electrode structure.     

Rapid fabrication of porous silicon/carbon microtube composites as anode materials for lithium-ion batteries

Herein, we present a simple and rapid method to synthesize porous silicon/carbon microtube composites (PoSi/CMTs) by adopting a unique configuration of acid etching solution. The CMTs can act as both conductive agent and buffer for Si volume change during the charge and discharge process. The highly reversible capacity and excellent rate capability can be ascribed to the structure, where porous silicon powders are wrapped by a network of interwoven carbon microtubes. The composites show specific capacities of more than 1712 mA h g⁻¹ at a current density of 100 mA g⁻¹, 1566 mA h g⁻¹ at 200 mA g⁻¹, 1407 mA h g⁻¹ at 400 mA g⁻¹, 1177 mA h g⁻¹ at 800 mA g⁻¹, 1107 mA h g⁻¹ at 1000 mA g⁻¹, 798 mA hg⁻¹ at 2000 mA g⁻¹, and 581 mA h g⁻¹ at 3000 mA g⁻¹ and maintain a value of 1127 mA h g⁻¹ after 100 cycles at a current density of 200 mA g⁻¹. Electrochemical impedance spectroscopy (EIS) measurements prove that charge transfer resistance of PoSi/CMT composites is smaller than that of pure PoSi. In this study, we propose a quick, economical and feasible method to prepare silicon-based anode materials for lithium-ion batteries.

We added additives to the acid etching solution and prepared the silicon/carbon microtubes composites using a simple and fast method.     

Facile synthesis of Camellia oleifera shell-derived hard carbon as an anode material for lithium-ion batteries

A comparatively facile and ecofriendly process has been developed to synthesize porous carbon materials from Camellia oleifera shells. Potassium carbonate solution (K₂CO₃) impregnation is introduced to modify the functional groups on the surface of Camellia oleifera shells, which may play a role in promoting the development of pore structure during carbonization treatment. Moreover, a small amount of naturally embedded nitrogen and sulfur in the Camellia oleifera shells can also bring about the formation of pores. The Camellia oleifera shell-derived carbon has a large specific surface area of 1479 m² g⁻¹ with a total pore volume of 0.832 cm³ g⁻¹ after being carbonized at 900 °C for 1 h. Furthermore, when used as an anode for lithium-ion batteries, the sample shows superior electrochemical performance with a specific capacity of 483 mA h g⁻¹ after 100 cycles measured at 200 mA g⁻¹ current density. Surprisingly, the specific capacity is even gradually increased with cycling. In addition, this sample exhibits almost 100% retention capacity after 250 cycles at a current density of 200 mA g⁻¹.

Bio-waste Camellia oleifera shells (COS) are converted into porous carbon by a two-step method.     

Carbon-coated SnO2 riveted on a reduced graphene oxide composite (C@SnO2/RGO) as an anode material for lithium-ion batteries

The research on graphene-based anode materials for high-performance lithium-ion batteries (LIBs) has been prevalent in recent years. In the present work, carbon-coated SnO₂ riveted on a reduced graphene oxide sheet composite (C@SnO₂/RGO) was fabricated using GO solution, SnCl₄, and glucose via a hydrothermal method after heat treatment. When the composite was exploited as an anode material for LIBs, the electrodes were found to exhibit a stable reversible discharge capacity of 843 mA h g⁻¹ at 100 mA g⁻¹ after 100 cycles with 99.5% coulombic efficiency (CE), and a specific capacity of 485 mA h g⁻¹ at 1000 mA g⁻¹ after 200 cycles; these values were higher than those for a sample without glucose (SnO₂/RGO) and a pure SnO₂ sample. The favourable electrochemical performances of the C@SnO₂/RGO electrodes may be attributed to the special double-carbon structure of the composite, which can effectively suppress the volume expansion of SnO₂ nanoparticles and facilitate the transfer rates of Li⁺ and electrons during the charge/discharge process.

The combined action of GO and glucose makes the SnO₂ dispersed uniformly. The synergistic effect of the unique double-carbon structure can effectively improve the electrical conductivity of the SnO₂ and strengthen lithium storage capability.     

Self-assembled hierarchical porous NiMn2O4 microspheres as high performance Li-ion battery anodes

Hierarchical structured porous NiMn₂O₄ microspheres assembled with nanorods are synthesized through a simple hydrothermal method followed by calcination in air. As anode materials for lithium ion batteries (LIBs), the NiMn₂O₄ microspheres exhibit a high specific capacity. The initial discharge capacity is 1126 mA h g⁻¹. After 1000 cycles, the NiMn₂O₄ demonstrates a reversible capacity of 900 mA h g⁻¹ at a current density of 500 mA g⁻¹. In particular, the porous NiMn₂O₄ microspheres still could deliver a remarkable discharge capacity of 490 mA h g⁻¹ even at a high current density of 2 A g⁻¹, indicating their potential application in Li-ion batteries. This excellent electrochemical performance is ascribed to the unique hierarchical porous structure which can provide sufficient contact for the transfer of Li⁺ ion and area for the volume change of the electrolyte leading to enhanced Li⁺ mobility.

Hierarchical structured porous NiMn₂O₄ microspheres assembled with nanorods are synthesized through a simple hydrothermal method followed by calcination in air.     

Constructing high-performance electrode materials using core–shell ZnCo2O4@PPy nanowires for hybrid batteries and water splitting

Heterogeneity can be used as a promising method to improve the electrochemical performance of electrode materials; thus, ZnCo₂O₄@PPy samples were prepared using a facile hydrothermal route and an electrochemical deposition process. The as-prepared products possess a specific capacitance of 605 C g⁻¹ at a current density of 1 A g⁻¹. The asymmetric supercapacitor (ASC) possesses an energy density of 141.3 W h kg⁻¹ at a power density of 2700.5 W kg⁻¹ and capacity retention of 88.1% after 10 000 cycles, indicating its promising potential for energy devices. ZnCo₂O₄@PPy-50 exhibited an excellent OER performance and outstanding HER performance in alkaline media. As an advanced bifunctional electrocatalyst for overall water splitting, a voltage of 1.61 V at a current density of 50 mA cm⁻² outperforms the majority of noble-metal-free electrocatalysts.

Heterogeneity can be used as a promising method to improve the electrochemical performance of electrode materials; thus, ZnCo₂O₄@PPy samples were prepared using a facile hydrothermal route and an electrochemical deposition process.     

Top-down strategy synthesis of fluorinated graphdiyne for lithium ion battery

As a novel carbon allotrope, graphdiyne exhibits excellent electrochemical properties such as high specific capacities, outstanding rate performances, and long cycle lives. These properties are attributed to its sp- and sp²-hybridized bonding and a natural large pore structure. Doping with light elements is a facile way to improve the electrochemical performance of graphdiyne. Herein, we report the preparation of fluorine-doped graphdiyne by exposure to XeF₂ under a mild temperature. Compared to pristine graphdiyne, the capacities are doubled. We obtained reversible capacities of fluorinated graphdiyne up to 1080 mA h g⁻¹ after 600 cycles at a current density of 500 mA g⁻¹. At a higher current density of 1000 mA g⁻¹, it still retained a high specific capacity of 693 mA h g⁻¹ after 1000 cycles. Using in situ quantitative nanomechanical probe atomic force microscopy, we further analyzed the surface morphologies and elastic modulus to understand the mechanism of the electrochemical improvement. The fluorinated graphdiyne elastic modulus is doubled in contrast to pristine graphdiyne. The performance improvements are attributed to the improvement in conductivity and enhancement of the mechanical properties.

Fluorine doped graphdiyne was synthesized by exposure to XeF₂ under mild temperature. Owing to the enhanced conductivity and enhanced mechanical properties, the electrochemical performances are significantly improved.     

Two-dimensional SnO2 anchored biomass-derived carbon nanosheet anode for high-performance Li-ion capacitors

Lithium-ion capacitors (LICs) combine the advantages of both batteries and supercapacitors; they have attracted intensive attention among energy conversion and storage fields, and one of the key points of their research is the exploration of suitable battery-type electrode materials. Herein, a simple and low-cost strategy is proposed, in which SnO₂ particles are anchored on the conductive porous carbon nano-sheets (PCN) derived from coffee grounds. This method can inhibit the grain coarsening of Sn and the volume change of SnO₂ effectively, thus improving the electrochemical reversibility of the materials. In the lithium half cell (0–3.0 V vs. Li/Li⁺), the as-prepared SnO₂/PCN electrode yields a reversible capacity of 799 mA h g⁻¹ at 0.1 A g⁻¹ and decent long-term cyclability of 313 mA h g⁻¹ at 1 A g⁻¹ after 500 cycles. The excellent Li⁺ storage performance of SnO₂/PCN is beneficial from the hierarchical structure as well as the robust carbonaceous buffer layer. Besides, a LIC hybrid device with the as-prepared SnO₂/PCN anode exhibits outstanding energy and power density of 138 W h kg⁻¹ and 53 kW kg⁻¹ at a voltage window of 1.0–4.0 V. These promising results open up a new way to develop advanced anode materials with high rate and long life.

In this work, we have fabricated lithium-ion capacitor using SnO₂/PCN as anode and waste coffee grounds derived PCN as cathode, which delivers good combination of high energy and power characteristics.     

Preparation and lithium storage of core–shell honeycomb-like Co3O4@C microspheres

Core–shell honeycomb-like Co₃O₄@C microspheres were synthesized via a facile solvothermal method and subsequent annealing treatment under an argon atmosphere. Owing to the core–shell honeycomb-like structure, a long cycling life was achieved (a high reversible specific capacity of 318.9 mA h g⁻¹ was maintained at 5C after 1000 cycles). Benefiting from the coated carbon layers, excellent rate capability was realized (a reversible specific capacity as high as 332.6 mA h g⁻¹ was still retained at 10C). The design of core–shell honeycomb-like microspheres provides a new idea for the development of anode materials for high-performance lithium-ion batteries.

The reversible specific capacity of CSHCo₃O₄@C microspheres was as high as 332.6 mA h g⁻¹ at 10C, which was significantly higher than that of SCo₃O₄ microspheres (68.7 mA h g⁻¹).     

Engineering NiCo2S4 nanoparticles anchored on carbon nanotubes as superior energy-storage materials for supercapacitors

Fabricating high-capacity electrode materials toward supercapacitors has attracted increasing attention. Here we report a three-dimensional CNTs/NiCo₂S₄ nanocomposite material synthesized successfully by a facile one-step hydrothermal technique. As expected, a CNTs/NiCo₂S₄ electrode shows remarkable capacitive properties with a high specific capacitance of 890 C g⁻¹ at 1 A g⁻¹. It also demonstrates excellent cycle stability with an 83.5% capacitance retention rate after 5000 cycles at 10 A g⁻¹. Importantly, when assembled into a asymmetric supercapacitor, it exhibits a high energy density (43.3 W h kg⁻¹) and power density (800 W kg⁻¹). The exceptional electrochemical capacity is attributed to the structural features, refined grains, and enhanced conductivity. The above results indicate that CNTs/NiCo₂S₄ composite electrode materials have great potential application in energy-storage devices.

A one-step hydrothermal method was used to successfully synthesize NiCo₂S₄ nanocomposites anchored on carbon nanotubes as excellent energy storage materials for supercapacitors.     

Enhanced storage behavior of quasi-solid-state aluminum–selenium battery

The current aluminum batteries with selenium positive electrodes have been suffering from dramatic capacity loss owing to the dissolution of Se₂Cl₂ products on the Se positive electrodes in the ionic liquid electrolyte. For addressing this critical issue and achieving better electrochemical performances of rechargeable aluminum–selenium batteries, here a gel-polymer electrolyte which has a stable and strongly integrated electrode/electrolyte interface was adopted. Quite intriguingly, such a gel-polymer electrolyte enables the solid-state aluminum–selenium battery to present a lower self-discharge and obvious discharging platforms. Meanwhile, the discharge capacity of the aluminum–selenium battery with a gel-polymer electrolyte is initially 386 mA h g⁻¹ (267 mA h g⁻¹ in ionic liquid electrolyte), which attenuates to 79 mA h g⁻¹ (32 mA h g⁻¹ in ionic liquid electrolyte) after 100 cycles at a current density of 200 mA g⁻¹. The results suggest that the employment of a gel-polymer electrolyte can provide an effective route to improve the performance of aluminum–selenium batteries in the first few cycles.

A quasi-solid-state aluminum–selenium battery has been established using gel-polymer electrolyte between the Se positive electrode and Al negative electrode which increasing the utilization of the active materials.     

Preparation of SiO2 nanowire arrays as anode material with enhanced lithium storage performance

SiO₂ nanowire arrays have been prepared by a template-assisted sol gel method and used as a negative electrode material for lithium ion batteries. Amorphous SiO₂ was confirmed by X-ray diffraction and Fourier transform infrared spectroscopy. The results of scanning electron microscopy and transmission electron microscopy confirmed that the SiO₂ nanowire had a diameter of about 100 nm and a length of about 30 μm. Cyclic voltammetry and constant current charge and discharge tests showed the prepared SiO₂ nanowire arrays were electrochemically active at a potential range of 0.05–3.0 V. At a current density of 200 mA g⁻¹, the first discharge specific capacity was as high as 2252.6 mA h g⁻¹ with a coulombic efficiency of 60.7%. Even after about 400 cycles, it still maintained 97.5% of the initial specific capacity. Moreover, a high specific capacity of 315 mA h g⁻¹ was exhibited when the current density was increased to 2500 mA g⁻¹. SiO₂ nanowire array electrodes with high reversible capacity and good cycle performance provide potential anode materials for future lithium-ion batteries.

SiO₂ nanowire arrays were synthesized using an AAO template-assisted sol–gel method. As a lithium negative electrode material, the sample exhibited excellent electrochemical properties.     

Three-dimensional thiophene-diketopyrrolopyrrole-based molecules/graphene aerogel as high-performance anode material for lithium-ion batteries

Herein, 3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione (TDPP) and di-tert-butyl 2,2′-(1,4-dioxo-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-2,5(1H,4H)-diyl)diacetate (TDPPA) were synthesized, which were then loaded in graphene aerogels. The as-prepared thiophene-diketopyrrolopyrrole-based molecules/reduced graphene oxide composites for lithium-ion battery (LIB) anode composites consist of DPPs nanorods on a graphene network. In relation to the DPPs part, embedding DPPs nanorods into graphene aerogels can effectively reduce the dissolution of DPPs in the electrolyte. It can serve to prevent electrode rupture and improve electron transport and lithium-ion diffusion rate, by partially connecting DPPs nanorods through graphene. The composite not only has a high reversible capacity, but also shows excellent cycling stability and performance, due to the densely distributed graphene nanosheets forming a three-dimensional conductive network. The TDPP₆₀ electrode exhibits high reversible capacity and excellent performance, showing an initial discharge capacity of 835 mA h g⁻¹ at a current density of 100 mA g⁻¹. Even at a current density of 1000 mA g⁻¹, after 500 cycles, it still demonstrates a discharge capacity of 303 mA h g⁻¹ with a capacity retention of 80.7%.

Herein, TDPP and TDPPA were synthesized and then loaded on graphene by hydrothermal method to obtain TDPP/RGO and TDPPA/RGO aerogel, which were applied as anode for LiBs.     

Hierarchical porous ZnMnO3 yolk–shell microspheres with superior lithium storage properties enabled by a unique one-step conversion mechanism

ZnMnO₃ has attracted enormous attention as a novel anode material for rechargeable lithium-ion batteries due to its high theoretical capacity. However, it suffers from capacity fading because of the large volumetric change during cycling. Here, porous ZnMnO₃ yolk–shell microspheres are developed through a facile and scalable synthesis approach. This ZnMnO₃ can effectively accommodate the large volume change upon cycling, leading to an excellent cycling stability. When applying this ZnMnO₃ as the anode in lithium-ion batteries, it shows a remarkable reversible capacity (400 mA h g⁻¹ at a current density of 400 mA g⁻¹ and 200 mA h g⁻¹ at 6400 mA g⁻¹) and excellent cycling performance (540 mA h g⁻¹ after 300 cycles at 400 mA g⁻¹) due to its unique structure. Furthermore, a novel conversion reaction mechanism of the ZnMnO₃ is revealed: ZnMnO₃ is first converted into intermediate phases of ZnO and MnO, after which MnO is further reduced to metallic Mn while ZnO remains stable, avoiding the serious pulverization of the electrode brought about by lithiation of ZnO.

ZnMnO₃ has attracted enormous attention as a novel anode material for rechargeable lithium-ion batteries due to its high theoretical capacity.     

Fabrication of NiO–carbon nanotube/sulfur composites for lithium-sulfur battery application

The practical applications of lithium–sulfur batteries are still a great challenge due to the polysulfide shuttle and capacity decay. Herein, we report a NiO–carbon nanotube/sulfur (NiO–CNT/S) composite by hydrothermal and thermal treatments. This hybrid combines the high conductivity of CNTs and double adsorption of CNTs and NiO (physical and chemical adsorption) to improve the electrochemical performance for the sulfur electrodes. Compared with CNT/S and NiO/S, the developed NiO–CNT/S composites present a preferable initial reversible discharge capacity (1072 mA h g⁻¹) and is maintained at 609 mA h g⁻¹ after 160 cycles at 0.1C.

The NiO–CNT/S composites combine the high conductivity of CNT and double adsorption of CNT and NiO (physical adsorption and chemical adsorption) to enhance electrochemical performance for sulfur electrode materials.