Improved pseudocapacitive charge storage in highly ordered mesoporous TiO2/carbon nanocomposites as high-performance Li-ion hybrid supercapacitor anodes

A Li-ion hybrid supercapacitor (Li-HSCs), an integrated system of a Li-ion battery and a supercapacitor, is an important energy-storage device because of its outstanding energy and power as well as long-term cycle life. In this work, we propose an attractive material (a mesoporous anatase titanium dioxide/carbon hybrid material, m-TiO₂-C) as a rapid and stable Li⁺ storage anode material for Li-HSCs. m-TiO₂-C exhibits high specific capacity (∼198 mA h g⁻¹ at 0.05 A g⁻¹) and promising rate performance (∼90 mA h g⁻¹ at 5 A g⁻¹) with stable cyclability, resulting from the well-designed porous structure with nanocrystalline anatase TiO₂ and conductive carbon. Thereby, it is demonstrated that a Li-HSC system using a m-TiO₂-C anode provides high energy and power (∼63 W h kg⁻¹, and ∼4044 W kg⁻¹).

A mesoporous TiO₂/carbon nanocomposite prepared by block copolymer self-assembly improves pseudocapacitive behavior and achieves high energy/power density Li-ion hybrid supercapacitors.     

Substantially enhanced rate capability of lithium storage in Na2Ti6O13 with self-doping and carbon-coating

Na₂Ti₆O₁₃ (NTO) has recently been reported for lithium ion storage and showed very promising results. In this work, we report substantially enhanced rate capability in NTO nanowires by Ti(iii) self-doping and carbon-coating. Ti(iii) doping and carbon coating were found to work in synergy to increase the electrochemical performances of the material. For 300 cycles at 1C (1C = 200 mA g⁻¹) the charge capacity of the electrode is 206 mA h g⁻¹, much higher than that (89 mA h g⁻¹) of the pristine NTO electrode. For 500 cycles at 5C the electrode can still deliver a charge capacity of 180.5 mA h g⁻¹ with a high coulombic efficiency of 99%. At 20C the capacity of the electrode is 2.6 times that of the pristine NTO. These results clearly demonstrate that the Ti(iii) self-doping and uniform carbon coating significantly enhanced the kinetic processes in the NTO nanowire crystal, making it possible for fast charge and discharge in Li-ion batteries.

Ti³⁺ self-doping and carbon-coating are efficient approaches to simultaneously improve the rate capability and cyclability of Na₂Ti₆O₁₃ nanowires for lithium storage.     

An investigation of Li2TiO3–coke composite anode material for Li-ion batteries

Anode material Li₂TiO₃–coke was prepared and tested for lithium-ion batteries. The as-prepared material exhibits excellent cycling stability and outstanding rate performance. Charge/discharge capacities of 266 mA h g⁻¹ at 0.100 A g⁻¹ and 200 mA h g⁻¹ at 1.000 A g⁻¹ are reached for Li₂TiO₃–coke. A cycling life-time test shows that Li₂TiO₃–coke gives a specific capacity of 264 mA h g⁻¹ at 0.300 A g⁻¹ and a capacity retention of 92% after 1000 cycles of charge/discharge.

Anode material Li₂TiO₃–coke was prepared and tested for lithium-ion batteries. The as-prepared material exhibits excellent cycling stability and outstanding rate performance.     

Development of an efficient CVD technique to prepare TiO2/porous–carbon nanocomposites for high rate lithium-ion capacitors

Titanium dioxide is a promising electrode material for lithium-ion capacitors. When using TiO₂ as an electrode material, it is necessary to combine it with carbon at the nanometer level to improve its low electrical conductivity and low reactivity with Li⁺. However, preparation methods of reported TiO₂/porous–carbon nanocomposites are generally not cost-effective, and their productivities are low. In this study, the vacuum liquid-pulse chemical vapor deposition (VLP-CVD) technique was developed to easily prepare TiO₂/porous–carbon nanocomposites, where TiO₂ nanoparticles with a diameter of ∼4 nm could be homogeneously deposited inside the pores of meso- or macroporous carbons. Because the deposited TiO₂ nanoparticles had access to effective electrically conductive paths formed by the porous–carbon substrate, they showed a high discharge capacity of ∼200 mA h g⁻¹-TiO₂ (based on TiO₂ weight). In particular, the composite prepared from macroporous carbon showed an extremely high rate performance, where 50% of the discharge capacity was retained at a current density of 15 000 mA g⁻¹ when compared to that measured at 50 mA g⁻¹. In addition, the composite also showed very high cyclability, where 80% of the discharge capacity was retained at the 10 000^th cycle. Because the VLP-CVD technique can be performed using simple apparatus and commercially available starting materials, it can be expected to boost industrial production of TiO₂/porous–carbon for lithium-ion capacitors.

TiO₂ nanoparticles with a diameter of around 5 nm were homogeneously deposited inside the pores of meso-macroporous carbons.     

Rigid TiO2−x coated mesoporous hollow Si nanospheres with high structure stability for lithium-ion battery anodes

Rigid oxygen-deficient TiO_2−x coated mesoporous hollow Si nanospheres with a mechanically and electrically robust structure have been constructed through a facile method for high-performance Li-ion battery anodes. The mesoporous hollow structure provides enough inner void space for the expansion of Si. The oxygen-deficient TiO_2−x coating has functions in three aspects: (1) avoiding direct contact between Si and the electrolyte; (2) suppressing the outward expansion of the mesoporous hollow Si nanospheres; (3) improving the conductivity of the composite. The combined effect leads to high interfacial stability and structural integrity of both the material nanoparticles and the whole electrode. By virtue of the rational design, the composite yields a high reversible specific capacity of 1750.4 mA h g⁻¹ at 0.2 A g⁻¹, an excellent cycling stability of 1303.1 mA h g⁻¹ at 2 A g⁻¹ with 84.5% capacity retention after 500 cycles, and a high rate capability of 907.6 mA h g⁻¹ even at 4 A g⁻¹.

A conductive TiO_2−x shell suppresses the outward expansion of Si to maintain high interfacial stability and structural integrity.     

Suppressing self-discharge of Li–B/CoS2 thermal batteries by using a carbon-coated CoS2 cathode

Thermal batteries with molten salt electrolytes are used for many military applications, primarily as power sources for guided missiles. The Li–B/CoS₂ couple is designed for high-power, high-voltage thermal batteries. However, their capacity and safe properties are influenced by acute self-discharge that results from the dissolved lithium anode in molten salt electrolytes. To solve those problems, in this paper, carbon coated CoS₂ was prepared by pyrolysis reaction of sucrose at 400 °C. The carbon coating as a physical barrier can protect CoS₂ particles from damage by dissolved lithium and reduce the self-discharge reaction. Therefore, both the discharge efficiency and safety of Li–B/CoS₂ thermal batteries are increased remarkably. Discharge results show that the specific capacity of the first discharge plateau of carbon-coated CoS₂ is 243 mA h g⁻¹ which is 50 mA h g⁻¹ higher than that of pristine CoS₂ at a current density of 100 mA cm⁻². The specific capacity of the first discharge plateau at 500 mA cm⁻² for carbon-coated CoS₂ and pristine CoS₂ are 283 mA h g⁻¹ and 258 mA h g⁻¹ respectively. The characterizations by XRD and DSC indicate that the carbonization process has no noticeable influence on the intrinsic crystal structure and thermal stability of pristine CoS₂.

Suppressing self-discharge of Li–B/CoS₂ thermal batteries through modifying the CoS₂ cathode with a protective carbon coating layer.     

TiO2–Au composite nanofibers for photocatalytic hydrogen evolution

TiO₂-based materials for photocatalytic hydrogen (H₂) evolution have attracted much interest as a renewable approach for clean energy applications. TiO₂–Au composite nanofibers (NFs) with an average fiber diameter of ∼160 nm have been fabricated by electrospinning combined with calcination treatment. In situ reduced gold nanoparticles (NPs) with uniform size (∼10 nm) are found to disperse homogenously in the TiO₂ NF matrix. The TiO₂–Au composite NFs catalyst can significantly enhance the photocatalytic H₂ generation with an extremely high rate of 12 440 μmol g⁻¹ h⁻¹, corresponding to an adequate apparent quantum yield of 5.11% at 400 nm, which is 25 times and 10 times those of P25 (584 μmol g⁻¹ h⁻¹) and pure TiO₂ NFs (1254 μmol g⁻¹ h⁻¹), respectively. Furthermore, detailed studies indicate that the H₂ evolution efficiency of the TiO₂–Au composite NF catalyst is highly dependent on the gold content. This work provides a strategy to develop highly efficient catalysts for H₂ evolution.

The H₂ production rate of TiO₂–Au nanofibers is dramatically improved to 12 440 μmol g⁻¹ h⁻¹, 10 times that of pure TiO₂.     

Flexible C–Mo2C fiber film with self-fused junctions as a long cyclability anode material for sodium-ion battery

Electrospun carbon fiber films have high contact resistance at the fiber junctions, which causes poor cycling stability and limits their further improvement in energy storage performances. To eliminate the contact resistance of the film, we provide a new strategy to fuse the fiber junctions by introducing MoO₂ in the fibers, which replaces the C–C interface by a more active C–MoO₂–C interface at the fiber junction to promote mass transfer. MoO₂ reacts with C matrix to generate Mo₂C and form self-fused junctions during the carbonization process. Due to much lower charge transfer and sodium diffusion resistance, the C–Mo₂C fiber film with self-fused junctions shows much better cyclability with capacity retention of 90% after 2000 cycles at a constant current density of 1 A g⁻¹. Moreover, the Mo₂C particles provide many electrochemically active sites, leading to additional improvement in sodium storage. The C–Mo₂C fiber film has a capacity of 134 mA h g⁻¹ at 1 A g⁻¹ and a high capacity of 99 mA h g⁻¹ even at 5 A g⁻¹.

Fiber junctions were fused by introducing MoO₂, that eliminates the contact resistance at fiber junctions, and significantly improves the cyclability.     

Nanostructured diatom earth SiO2 negative electrodes with superior electrochemical performance for lithium ion batteries

Diatomaceous earth (DE) is a naturally occurring silica source constituted by fossilized remains of diatoms, a type of hard-shelled algae, which exhibits a complex hierarchically nanostructured porous silica network. In this work, we analyze the positive effects of reducing DE SiO₂ particles to the sub-micrometer level and implementing an optimized carbon coating treatment to obtain DE SiO₂ anodes with superior electrochemical performance for Li-ion batteries. Pristine DE with an average particle size of 17 μm is able to deliver a specific capacity of 575 mA h g⁻¹ after 100 cycles at a constant current of 100 mA g⁻¹, and reducing the particle size to 470 nm enhanced the reversible specific capacity to 740 mA h g⁻¹. Ball-milled DE particles were later subjected to a carbon coating treatment involving the thermal decomposition of a carbohydrate precursor at the surface of the particles. Coated ball-milled silica particles reached stable specific capacities of 840 mA h g⁻¹ after 100 cycles and displayed significantly improved rate capability, with discharge specific capacities increasing from 220 mA h g⁻¹ (uncoated ball-milled SiO₂) to 450 mA h g⁻¹ (carbon coated ball-milled SiO₂) at 2 A g⁻¹. In order to trigger SiO₂ reactivity towards lithium, all samples were subjected to an electrochemical activation procedure prior to electrochemical testing. XRD measurements on the activated electrodes revealed that the initial crystalline silica was completely converted to amorphous phases with short range ordering, therefore evidencing the effective role of the activation procedure.

Diatomaceous earth SiO₂ anodes with superior electrochemical performance are obtained by ball milling, carbon coating and electrochemical activation of SiO₂ particles.     

Rational synthesis of a hierarchical Mo2C/C nanosheet composite with enhanced lithium storage properties

Transition metal carbides have been studied extensively as anode materials for lithium-ion batteries (LIBs), but they suffer from sluggish lithium reaction kinetics and large volume expansion. Herein, a hierarchical Mo₂C/C nanosheet composite has been synthesized through a rational pyrolysis strategy, and evaluated as an anode material with enhanced lithium storage properties for LIBs. In the hierarchical Mo₂C/C nanosheet composite, large numbers of Mo₂C nanosheets with a thickness of 40–100 nm are uniformly anchored onto/into carbon nanosheet matrices. This unique hierarchical architecture can provide favorable ion and electron transport pathways and alleviate the volume change of Mo₂C during cycling. As a consequence, the hierarchical Mo₂C/C nanosheet composite exhibits high-performance lithium storage with a reversible capacity of up to 868.6 mA h g⁻¹ after 300 cycles at a current density of 0.2 A g⁻¹, as well as a high rate capacity of 541.8 mA h g⁻¹ even at 5.0 A g⁻¹. More importantly, this hierarchical composite demonstrates impressive cyclability with a capacity retention efficiency of 122.1% over 5000 successive cycles at 5.0 A g⁻¹, which surpasses the cycling properties of most other Mo₂C-based materials reported to date.

The hierarchical Mo₂C/C nanosheet composite exhibits excellent cyclability owing to its structural and kinetic advantages.     

Highly crystalline anatase TiO2 nanocuboids as an efficient photocatalyst for hydrogen generation

Highly crystalline anatase titanium dioxide (TiO₂) nanocuboids were synthesized via a hydrothermal method using ethylenediamine tetraacetic acid as a capping agent. The structural study revealed the nanocrystalline nature of anatase TiO₂ nanocuboids. Morphological study indicates the formation of cuboid shaped particles with thickness of ∼5 nm and size in the range of 10–40 nm. The UV-visible absorbance spectra of TiO₂ nanocuboids showed a broad absorption with a tail in the visible-light region which is attributed to the incorporation of nitrogen atoms into the interstitial positions of the TiO₂ lattice as well as the formation of carbonaceous and carbonate species on the surface of TiO₂ nanocuboids. The specific surface areas of prepared TiO₂ nanocuboids were found to be in the range of 85.7–122.9 m² g⁻¹. The formation mechanism of the TiO₂ nanocuboids has also been investigated. Furthermore, the photocatalytic activities of the as-prepared TiO₂ nanocuboids were evaluated for H₂ generation via water splitting under UV-vis light irradiation and compared with the commercial anatase TiO₂. TiO₂ nanocuboids obtained at 200 °C after 48 h exhibited higher photocatalytic activity (3866.44 μmol h⁻¹ g⁻¹) than that of commercial anatase TiO₂ (831.30 μmol h⁻¹ g⁻¹). The enhanced photoactivity of TiO₂ nanocuboids may be due to the high specific surface area, good crystallinity, extended light absorption in the visible region and efficient charge separation.

Highly crystalline TiO₂ nanocuboids have been prepared and their photocatalytic hydrogen generation activity was evaluated via water splitting.     

Ultrafast-charging and long cycle-life anode materials of TiO2-bronze/nitrogen-doped graphene nanocomposites for high-performance lithium-ion batteries

Emerging technologies demand a new generation of lithium-ion batteries that are high in power density, fast-charging, safe to use, and have long cycle lives. This work reports charging rates and specific capacities of TiO₂(B)/N-doped graphene (TNG) composites. The TNG composites were prepared by the hydrothermal method in various reaction times (3, 6, 9, 12, and 24 h), while the N-doped graphene was synthesized using the modified Hummer''s method followed by a heat-treatment process. The different morphologies of TiO₂ dispersed on the N-doped graphene sheet were confirmed as anatase-nanoparticles (3, 6 h), TiO₂(B)-nanotubes (9 h), and TiO₂(B)-nanorods (12, 24 h) by XRD, TEM, and EELS. In electrochemical studies, the best battery performance was obtained with the nanorods TiO₂(B)/N-doped graphene (TNG-24h) electrode, with a relatively high specific capacity of 500 mA h g⁻¹ at 1C (539.5 mA g⁻¹). In long-term cycling, excellent stability was observed. The capacity retention of 150 mA h g⁻¹ was observed after 7000 cycles, at an ultrahigh current of 50C (27.0 A g⁻¹). The synthesized composites have the potential for fast-charging and have high stability, showing potential as an anode material in advanced power batteries for next-generation applications.

The TiO₂-bronze/nitrogen-doped graphene nanocomposites have the potential for fast-charging and have high stability, showing potential as an anode material in advanced power batteries for next-generation applications.     

TiO2-decorated porous carbon nanofiber interlayer for Li–S batteries

Lithium–sulfur (Li–S) batteries are the most promising energy storage systems owing to their high energy density. However, shuttling of polysulfides detracts the electrochemical performance of Li–S batteries and thus prevents the commercialization of Li–S batteries. Here, TiO₂@porous carbon nanofibers (TiO₂@PCNFs) are fabricated via combining electrospinning and electrospraying techniques and the resultant TiO₂@PCNFs are evaluated for use as an interlayer in Li–S batteries. TiO₂ nanoparticles on PCNFs are observed from SEM and TEM images. A high initial discharge capacity of 1510 mA h g⁻¹ is achieved owing to the novel approach of electrospinning the carbon precursor and electrospraying TiO₂ nanoparticles simultaneously. In this approach TiO₂ nanoparticles capture polysulfides with strong interaction and the PCNFs with high conductivity recycle and re-use the adsorbed polysulfides, thus leading to high reversible capacity and stable cycling performance. A high reversible capacity of 967 mA h g⁻¹ is reached after 200 cycles at 0.2C. The cell with the TiO₂@PCNF interlayer also delivers a reversible capacity of around 1100 mA h g⁻¹ at 1C, while the cell without the interlayer exhibits a lower capacity of 400 mA h g⁻¹. Therefore, this work presents a novel approach for designing interlayer materials with exceptional electrochemical performance for high performance Li–S batteries.

Lithium–sulfur (Li–S) batteries are the most promising energy storage systems owing to their high energy density.     

TiO2-coated LiCoO2 electrodes fabricated by a sputtering deposition method for lithium-ion batteries with enhanced electrochemical performance

We fabricated lithium cobalt oxide (LiCoO₂, LCO) electrodes in the absence and presence of TiO₂ layers as cathodes for lithium-ion batteries (LIBs) using a sputtering deposition method under an Ar atmosphere. In particular, TiO₂ coating layers on sputtered LCO electrodes were directly deposited in a layer-by-layer form with varying TiO₂ sputtering times from 60 to 120 s. These sputtered electrodes were heated at 600 °C in an air atmosphere for 3 h. The thicknesses of TiO₂ layers in TiO₂-coated LCO electrodes were controlled from ∼2 to ∼10 nm. These TiO₂-coated LCO electrodes exhibited superior electrochemical performance, i.e. high capacities (93–107 mA h g⁻¹@0.5C), improved retention of >60% after 100 cycles, and high-rate cycling properties (64 mA h g⁻¹@1C after 100 cycles). Such an improved performance of TiO₂-coated LCO electrodes was found to be attributed to relieved volumetric expansion of LCO and protection of LCO electrodes against HF generated during cycling.

We fabricated lithium cobalt oxide (LiCoO₂, LCO) electrodes in the absence and presence of TiO₂ layers as cathodes for lithium-ion batteries (LIBs) using a sputtering deposition method under an Ar atmosphere.     

Dendritic nanostructured FeS2-based high stability and capacity Li-ion cathodes

Here we show that dendritic architectures are attractive as the basis of hierarchically structured battery electrodes. Dendritically structured FeS₂, synthesized via simple thermal sulfidation of electrodeposited dendritic α-Fe, was formed into an electrode and cycled vs. lithium. The reversible capacities of the dendritic FeS₂ cathode were 560 mA h g⁻¹ at 0.5C and 533 mA h g⁻¹ at 1.0C after 50 cycles over 0.7–3.0 V. Over 0.7–2.4 V, where the electrode is more stable, the reversible capacities are 348 mA h g⁻¹ at 0.2C and 179 mA h g⁻¹ at 1.0C after 150 cycles. The good cycling performance and high specific capacities of the dendritic FeS₂ cathodes are attributed to the ability of a dendritic structure to provide good ion and electron conducting pathways, and a large surface area. Importantly, the dendritic structure appears capable of accommodating volume changes imposed by the lithiation and delithiation process. The presence of a Li_2−xFeS₂ phase is indicated for the first time by high-resolution transmission electron microscopy (HRTEM) and scanning transmission electron microscopy (STEM) electron energy loss spectroscopy (EELS). We suspect this phase is what enables electrochemical cycling to possess high reversibility over 0.7–2.4 V.

High performance dendritically structured FeS₂ cathodes are systemically studied. The dendritic structure is resistant to volume changes during cycling, increasing cyclability. The presence of Li_2–xFeS₂, which also enhances cyclability, is confirmed.     

Fabrication of uniform urchin-like N-doped NiCo2O4@C hollow nanostructures for high performance supercapacitors

Transition metal oxides are commonly used in electrochemical energy storage materials, but there are still many drawbacks that impede a wide range of applications. Heteroatom doping can significantly improve its performance. Herein, we have successfully prepared highly uniform N-doped NiCo₂O₄@C hollow nanostructures for supercapacitors by a two-step hydrothermal treatment associated with successive annealing process. Prepared N-doped NiCo₂O₄@C materials exhibited an admirable specific capacitance of 1028 F g⁻¹ at a current density of 3 A g⁻¹, with 625 F g⁻¹ remaining even at high current density of 20 A g⁻¹. Besides, this composite showed good electrochemical stability with capacity retention of 84% after 5000 cycles repetitive galvanostatic charge–discharge test at 10 A g⁻¹. An asymmetric supercapacitor was assembled by the N-doped NiCo₂O₄@C electrode, attached activate carbon (AC) as a counter electrode, exhibiting a high energy density of 26.67 W h kg⁻¹ at a power density of 402 W kg⁻¹. The improvement of electrochemical performance is ascribed to the co-doping of nitrogen and carbon atoms. These results indicate that N-doped NiCo₂O₄@C can be employed as an ideal electrode material for electrochemical energy storage.

Procedure for fabricating N-doped NiCo₂O₄@C hollow nanostructures.     

Lichen-like anchoring of MoSe2 on functionalized multiwalled carbon nanotubes: an efficient electrode for asymmetric supercapacitors

In the present study, we have developed a composite electrode of MSNT using a simple and scalable two-step scheme to synthesize a composite electrode material comprising MoSe₂/multiwalled carbon nanotubes (MoSe₂/MWCNTs) for supercapacitor applications. First, a MWCNT thin film was deposited on a stainless steel substrate by using a “dip and dry” coating technique. Subsequently, MoSe₂ was deposited onto the MWCNT thin film using the successive ionic layer adsorption and reaction method. The lichen-like growth of MoSe₂ on the MWCNT network provided dual charge storage and an effective ion transfer path. The composite electrode of MSNT has been studied systematically with different electrolytes and concentrations of electrolyte. As a result, the MoSe₂/MWCNT (MSNT) electrode exhibited excellent electrochemical properties such as a specific capacity of 192 mA h g⁻¹ and a capacitance retention of 88% after 2000 cycles in 1 M LiCl electrolyte. The results demonstrated the huge potential of the MSNT composite electrode for practical application in supercapacitors. The aqueous symmetric cell fabricated using the MSNT composite as both the anode and cathode showed an energy density of 17.9 W h kg⁻¹. Additionally, the energy density improved by designing an asymmetric device of MSNT//MnO₂ and notably, it reveals two-fold improvement in the energy density compared to a symmetric MSNT cell. The MSNT//MnO₂-based asymmetric cell exhibited a maximum specific capacitance of 112 F g⁻¹ with a high energy density of 35.6 W h kg⁻¹.

Simple and scalable chemical synthesis approach to develop a MoSe₂/MWCNTs composite thin film electrode for a highly efficient asymmetric supercapacitor cell.     

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.     

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).     

Ultradispersed titanium dioxide nanoparticles embedded in a three-dimensional graphene aerogel for high performance sulfur cathodes

Lithium–sulfur (Li–S) batteries are regarded as one of the most promising energy storage technologies, however, their practical application is greatly limited by a series of sulfur cathode challenges such as the notorious “shuttle effect”, low conductivity and large volume change. Here, we develop a facile hydrothermal method for the large scale synthesis of sulfur hosts consisting of three-dimensional graphene aerogel with tiny TiO₂ nanoparticles (5–10 nm) uniformly dispersed on the graphene sheet (GA–TiO₂). The obtained GA–TiO₂ composites have a high surface area of ∼360 m² g⁻¹ and a hierarchical porous structure, which facilitates the encapsulation of sulfur in the carbon matrix. The resultant GA–TiO₂/S composites exhibit a high initial discharge capacity of 810 mA h g⁻¹ with an ultralow capacity fading of 0.054% per cycle over 700 cycles at 2C, and a high rate (5C) performance (396 mA h g⁻¹). Such architecture design paves a new way to synthesize well-defined sulfur hosts to tackle the challenges for high performance Li–S batteries.

GA–TiO₂ composites as a cathode material realize an excellent electrochemical performance in Li–S batteries.