Mixed transition metal oxides (MTMOs) have received intensive attention as promising anode materials for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). In this work, we demonstrate a facile one-step water-bath method for the preparation of graphene oxide (GO) decorated Fe2(MoO4)3 (FMO) microflower composite (FMO/GO), in which the FMO is constructed by numerous nanosheets. The resulting FMO/GO exhibits excellent electrochemical performances in both LIBs and SIBs. As the anode material for LIBs, the FMO/GO delivers a high capacity of 1,220 mAh·g–1 at 200 mA·g–1 after 50 cycles and a capacity of 685 mAh·g–1 at a high current density of 10 A·g–1. As the anode material for SIBs, the FMO/GO shows an initial discharge capacity of 571 mAh·g–1 at 100 mA·g–1, maintaining a discharge capacity of 307 mAh·g–1 after 100 cycles. The promising performance is attributed to the good electrical transport from the intimate contact between FMO and graphene oxide. This work indicates that the FMO/GO composite is a promising anode for high-performance lithium and sodium storage.
Scrupulous design and fabrication of advanced electrode materials are vital for developing high-performance sodium ion batteries. Herein, we report a facile one-step hydrothermal strategy for construction of a C-MoSe2/rGO composite with both high porosity and large surface area. Double modification of MoSe2 nanosheets is realized in this composite by introducing a reduced graphene oxide (rGO) skeleton and outer carbon protective layer. The MoSe2 nanosheets are well wrapped by a carbon layer and also strongly anchored on the interconnected rGO network. As an anode in sodium ion batteries, the designed C-MoSe2/rGO composite delivers noticeably enhanced sodium ion storage, with a high specific capacity of 445 mAh·g-1 at 200 mA·g-1 after 350 cycles, and 228 mAh·g-1 even at 4 A·g-1; these values are much better than those of C-MoSe2 nanosheets (258 mAh·g-1 at 200 mA·g-1 and 75 mAh·g-1 at 4 A·g-1). Additionally, the sodium ion storage mechanism is investigated well using ex situ X-ray diffraction and transmission electron microscopy methods. Our proposed electrode design protocol and sodium storage mechanism may pave the way for the fabrication of other high-performance metal diselenide anodes for electrochemical energy storage.
Rechargeable metal-iodine batteries are an emerging attractive electrochemical energy storage technology that combines metallic anodes with halogen cathodes. Such batteries using aqueous electrolytes represent a viable solution for the safety and cost issues associated with organic electrolytes. A hybrid-electrolyte battery architecture has been adopted in a lithium-iodine battery using a solid ceramic membrane that protects the metallic anode from contacting the aqueous electrolyte. Here we demonstrate an eco-friendly, low-cost zinc-iodine battery with an aqueous electrolyte, wherein active I2 is confined in a nanoporous carbon cloth substrate. The electrochemical reaction is confined in the nanopores as a single conversion reaction, thus avoiding the production of I3? intermediates. The cathode architecture fully utilizes the active I2, showing a capacity of 255 mAh·g?1 and low capacity cycling fading. The battery provides an energy density of ～ 151 Wh·kg?1 and exhibits an ultrastable cycle life of more than 1,500 cycles.
The assembly of hybrid nanomaterials has opened up a new direction for the construction of high-performance anodes for lithium-ion batteries (LIBs). In this work, we present a straightforward, eco-friendly, one-step hydrothermal protocol for the synthesis of a new type of Fe2O3-SnO2/graphene hybrid, in which zero-dimensional (0D) SnO2 nanoparticles with an average diameter of 8 nm and one-dimensional (1D) Fe2O3 nanorods with a length of ~150 nm are homogeneously attached onto two-dimensional (2D) reduced graphene oxide nanosheets, generating a unique point-line-plane (0D-1D-2D) architecture. The achieved Fe2O3-SnO2/graphene exhibits a well-defined morphology, a uniform size, and good monodispersity. As anode materials for LIBs, the hybrids exhibit a remarkable reversible capacity of 1,530 mA·g?1 at a current density of 100 mA·g?1 after 200 cycles, as well as a high rate capability of 615 mAh·g?1 at 2,000 mA·g?1. Detailed characterizations reveal that the superior lithium-storage capacity and good cycle stability of the hybrids arise from their peculiar hybrid nanostructure and conductive graphene matrix, as well as the synergistic interaction among the components.
Nanomaterials with electrochemical activity are always suffering from aggregations, particularly during the high-temperature synthesis processes, which will lead to decreased energy-storage performance. Here, hierarchically structured lithium titanate/nitrogen-doped porous graphene fiber nanocomposites were synthesized by using confined growth of Li4Ti5O12 (LTO) nanoparticles in nitrogen-doped mesoporous graphene fibers (NPGF). NPGFs with uniform pore structure are used as templates for hosting LTO precursors, followed by high-temperature treatment at 800 °C under argon (Ar). LTO nanoparticles with size of several nanometers are successfully synthesized in the mesopores of NPGFs, forming nanostructured LTO/NPGF composite fibers. As an anode material for lithium-ion batteries, such nanocomposite architecture offers effective electron and ion transport, and robust structure. Such nanocomposites in the electrodes delivered a high reversible capacity (164 mAh·g–1 at 0.3 C), excellent rate capability (102 mAh·g–1 at 10 C), and long cycling stability.
We report the synthesis and electrochemical sodium storage of cobalt disulfide (CoS2) with various micro/nano-structures. CoS2 with microscale sizes are either assembled by nanoparticles (P-CoS2) via a facile solvothermal route or nanooctahedrons constructed solid (O-CoS2) and hollow microstructures (H-CoS2) fabricated by hydrothermal methods. Among three morphologies, H-CoS2 exhibits the largest discharge capacities and best rate performance as anode of sodium-ion batteries (SIBs). Furthermore, H-CoS2 delivers a capacity of 690 mA·h·g?1 at 1 A·g?1 after 100 cycles in a potential range of 0.1–3.0 V, and ～240 mA·h·g?1 over 800 cycles in the potential window of 1.0–3.0 V. This cycling difference mainly lies in the two discharge plateaus observed in 0.1–3.0 V and one discharge plateau in 1.0–3.0 V. To interpret the reactions, X-ray diffraction (XRD) and transmission electron microscopy (TEM) are applied. The results show that at the first plateau around 1.4 V, the insertion reaction (CoS2 + xNa+ + xe? → NaxCoS2) occurs; while at the second plateau around 0.6 V, the conversion reaction (NaxCoS2 + (4 ? x) Na+ + (4 ? x)e? → Co + 2Na2S) takes place. This provides insights for electrochemical sodium storage of CoS2 as the anode of SIBs.
T-Nb2O5/reduced graphene oxide nanohybrids were fabricated via the hydrothermal attachment of Nb2O5 nanowires to dispersed graphene oxide nanosheets followed by a high-temperature phase transformation. Electrochemical measurements showed that the nanohybrid anodes possessed enhanced reversible capacity and superior cycling stability compared to those of a pristine T-Nb2O5 nanowire electrode. Owing to the strong bonds between graphene nanosheets and T-Nb2O5 nanowires, the nanohybrids achieved an initial capacity of 227 mAh·g?1. Additionally, non-aqueous asymmetric supercapacitors (ASCs) were fabricated with the synthesized nanohybrids as the anode and activated carbon as the cathode. The 3 V Li-ion ASC with a LiPF6-based organic electrolyte achieved an energy density of 45.1 Wh·kg?1 at 715.2 W·kg?1. The working potential could be further enhanced to 4 V when a polymer ionogel separator (PVDF-HFP/LiTFSI/EMIMBF4) and formulated ionic liquid electrolyte were employed. Such a quasi-solid state ASC could operate at 60 °C and delivered a maximum energy density of 70 Wh·kg?1 at 1 kW·kg?1.
Triangular Ni(HCO3)2 nanosheets were synthesized via a template-free solvothermal method. The phase transition and formation mechanism were explored systematically. Further investigation indicated that the reaction time and pH have significant effects on the morphology and size distribution of the triangular Ni(HCO3)2 nanosheets. More interestingly, the resulting product had an ultra-thin structure and high specific surface area, which can effectively accelerate the charge transport during charge–discharge processes. As a result, the triangular Ni(HCO3)2 nanosheets not only exhibited high specific capacitance (1,797 F·g-1 at 5 A·g-1 and 1,060 F·g-1 at 50 A·g-1), but also showed excellent cycling stability with a high current density (~80% capacitance retention after 5,000 cycles at the current density of 20 A·g-1).
Iron oxides have attracted considerable interest as abundant materials for high-capacity Li-ion battery anodes. However, their fast capacity fading owing to poorly controlled reversibility of the conversion reactions greatly hinders their application. Here, a sandwich-structured nanocomposite of N-doped graphene and nearly monodisperse Fe3O4 nanoparticles were developed as high-performance Li-ion battery anode. N-doped graphene serves as a conducting framework for the self-assembled structure and controls Fe3O4 nucleation through the interaction of N dopants, surfactant molecules, and iron precursors. Fe3O4 nanoparticles were well dispersed with a uniform diameter of ~15 nm. The unique sandwich structure enables good electron conductivity and Li-ion accessibility and accommodates a large volume change. Hence, it delivers good cycling reversibility and rate performance with a capacity of ~1,227 mA·h·g–1 and 96.8% capacity retention over 1,000 cycles at a current density of 3 A·g–1. Our work provides an ideal structure design for conversion anodes or other electrode materials requiring a large volume change.
The construction of metal sulfides-carbon nanocomposites with a hollow structure is highly attractive for various energy storage and conversion technologies. Herein, we report a facile two-step method for preparing a nanocomposite with CoS2 nanoparticles in N-doped carbon nanotube hollow frameworks (NCNTFs). Starting from zeolitic imidazolate framework-67 (ZIF-67) particles, in situ reduced metallic cobalt nanocrystals expedite the formation of the hierarchical hollow frameworks from staggered carbon nanotubes via a carbonization process. After a follow-up sulfidation reaction with sulfur powder, the embedded cobalt crystals are transformed into CoS2 nanoparticles. Benefitting from the robust hollow frameworks made of N-doped carbon nanotubes and highly active CoS2 ultrafine nanoparticles, this advanced nanocomposite shows greatly enhanced lithium storage properties when evaluated as an electrode for lithium-ion batteries. Impressively, the resultant CoS2/NCNTF material delivers a high specific capacity of ～937 mAh·g–1 at a current density of 1.0 A·g–1 with a cycle life longer than 160 cycles.
We report the facile, one-pot synthesis of 3-D urchin-like W18O49 nanostructures (U-WO) via a simple solvothermal approach. An excellent supercapacitive performance was achieved by the U-WO because of its large Brunauer–Emmett–Teller (BET) specific surface area (ca. 123 m2·g–1) and unique morphological and structural features. The U-WO electrodes not only exhibit a high rate-capability with a specific capacitance (Csp) of ~235 F·g–1 at a current density of 20 A·g–1, but also superior long-life performance for 1,000 cycles, and even up to 7,000 cycles, showing ~176 F·g–1 at a high current density of 40 A·g–1.
This is the first report on the thermoelectric properties of a catalyst-free polyol method used to prepare stoichiometric Bi2?xCuxS3 samples, x = 0.1, 0.2, 0.3, 0.4, via hot pressing. Various systematic approaches to arrive at in their stoichiometric compositions are explored precisely with introduction of excess precursor of S. X-ray diffraction data analysis using Rietveld refinement confirms a polyhedral orthorhombic crystal structure with a space group Pnma, in contrast to Pbnm reported earlier. Raman data further substantiates this. X-ray photoelectron spectroscopy confirms the valence states of the constituent elements (Bi3+, Cu2+, and S2?) and energy dispersive X-ray analysis corroborates their compositions. The particle sizes of the pure Bi2S3 nanoparticles were 20, 35, and 82 nm as determined from the Scherrer formula, atomic force microscopy, and dynamic light scattering, respectively. Their transmission electron microscopy image shows rod-like nanostructures elongated in the 〈010〉 direction with an average diameter of 23 nm and a length of several hundreds of nanometers. A 34% improvement in the thermoelectric figure of merit is observed for Bi1.6Cu0.4S3 as compared to pure Bi2S3 at 300 K.
Sodium-ion batteries (SIBs) and potassium-ion batteries (PIBs) have been considered as attractive alternatives for next-generation battery systems, which have promising application potential due to their earth abundance of potassium and sodium, high capacity and suitable working potential, however, the design and application of bi-functional high-performance anode still remain a great challenge up to date. Bismuth sulfide is suitable as anode owing to its unique laminar structure with relatively large interlayer distance to accommodate larger radius ions, high theoretical capacity and high volumetric capacity etc. In this study, dandelion-like Bi2S3/rGO hierarchical microspheres as anode material for PIBs displayed reversible capacity, and 206.91 mAh·g−1 could be remained after 1,200 cycles at a current density of 100 mA·g−1. When applied as anode materials for SIBs, 300 mAh·g−1 could be retained after 300 cycles at 2 A·g−1 and its initial Coulombic efficiency is as high as 97.43%. Even at high current density of 10 A·g−1, 120.3 mAh·g−1 could be preserved after 3,400 cycles. The Na3V2(PO4)3@rGO//Bi2S3/rGO sodium ion full cells were successfully assembled which displays stable performance after 60 cycles at 100 mA·g−1. The above results demonstrate that Bi2S3/rGO has application potential as high performance bi-functional anode for PIBs and SIBs.
A highly active and stable oxygen evolution reaction (OER) electrocatalyst is critical for hydrogen production from water splitting. Herein, three-dimensional Ni3S2@graphene@Co92S8 (Ni3S2@G@Co9S8), a sandwich-structured OER electrocatalyst, was grown in situ on nickel foam; it afforded an enhanced catalytic performance when highly conductive graphene is introduced as an intermediary for enhancing the electron transfer rate and stability. Serving as a free-standing electrocatalytic electrode, Ni3S2@G@Co9S8 presents excellent electrocatalytic activities for OER: A low onset overpotential (2 mA·cm?2 at 174 mV), large anode current density (10 mA·cm?2 at an overpotential of 210 mV), low Tafel slope (66 mV·dec?1), and predominant durability of over 96 h (releasing a current density of ～14 mA·cm?2 with a low and constant overpotential of 215 mV) in a 1 M KOH solution. This work provides a promising, cost-efficient electrocatalyst and sheds new light on improving the electrochemical performance of composites through enhancing the electron transfer rate and stability by introducing graphene as an intermediary.
Spinel LiMn2O4 is a widely utilized cathode material for Li-ion batteries. However, its applications are limited by its poor energy density and power density. Herein, a novel hierarchical porous onion-like LiMn2O4(LMO) was prepared to shorten the Li+ diffusion pathway with the presence of uniform pores and nanosized primary particles. The growth mechanism of the porous onion-like LiMn2O4 was analyzed to control the morphology and the crystal structure so that it forms a polyhedral crystal structure with reduced Mn dissolution. In addition, graphene was added to the cathode (LiMn2O4/graphene) to enhance the electronic conductivity. The synthesized LiMn2O4/graphene exhibited an ultrahigh-rate performance of 110.4 mAh·g–1 at 50 C and an outstanding energy density at a high power density, maintaining 379.4 Wh·kg–1 at 25,293 W·kg–1. Besides, it shows durable stability, with only 0.02% decrease in the capacity per cycle at 10 C. Furthermore, the (LiMn2O4/graphene)/graphite full-cell exhibited a high discharge capacity. This work provides a promising method for the preparation of outstanding, integrated cathodes for potential applications in lithium ion batteries.
We systematically investigated the development of film morphology and crystallinity of methyl-ammonium bismuth (III) iodide (MA3Bi2I9) through onestep spin-coating on TiO2-deposited indium tin oxide (ITO)/glass. The precursor solution concentration and substrate structure have been demonstrated to be critically important in the active-layer evolution of the MA3Bi2I9-based solar cell. This work successfully improved the cell efficiency to 0.42% (average: 0.38%) with the mesoscopic architecture of ITO/compact-TiO2/mesoscopic-TiO2 (meso-TiO2)/MA3Bi2I9/2,2′,7,7′-tetrakis(N,N-di-4-methoxyphenylamino)-9,9′spiro-bifluorene (spiro-MeOTAD)/MoO3/Ag under a precursor concentration of 0.45 M, which provided the probability of further improving the efficiency of the Bi3+-based lead-free organic–inorganic hybrid solar cells.
Lithium iron silicate (Li2FeSiO4) is capable of affording a much higher capacity than conventional cathodes, and thus, it shows great promise for high-energy battery applications. However, its capacity has often been adversely affected by poor reaction activity due to the extremely low electronic and ionic conductivity of silicates. Here, we for the first time report on a rational engineering strategy towards a highly active Li2FeSiO4 by designing a carbon nanotube (CNT) directed three-dimensional (3D) porous Li2FeSiO4 composite. As the CNT framework enables rapid electron transport, and the rich pores allow efficient electrolyte penetration, this unique 3D Li2FeSiO4-CNT composite exhibits a high capacity of 214 mAh·g?1 and retains 96% of this value over 40 cycles, thus, outstripping many previously reported Li2FeSiO4-based materials. Kinetic analysis reveals a high Li+ diffusivity due to coupling of the migration of electrons and ions. This research highlights the potential for engineering 3D porous structure to construct highly efficient electrodes for battery applications.
Uniform colloidal Bi2S3 nanodots and nanorods with different sizes have been prepared in a controllable manner via a hot injection method. X-ray
diffraction (XRD) results show that the resulting nanocrystals have an orthorhombic structure. Both the diameter and length
of the nanorods increase with increasing concentration of the precursors. All of the prepared Bi2S3 nanostructures show high efficiency in the photodegradation of rhodamine B, especially in the case of small sized nanodots—which
is possibly due to their high surface area. The dynamics of the photocatalysis is also discussed.
相似文献
Sodium-ion batteries (SIBs) have great promise for sustainable and economical energy-storage applications. Nevertheless, it is a major challenge to develop anode materials with high capacity, high rate capability, and excellent cycling stability for them. In this study, FeSe2 clusters consisting of nanorods were synthesized by a facile hydrothermal method, and their sodium-storage properties were investigated with different electrolytes. The FeSe2 clusters delivered high electrochemical performance with an ether-based electrolyte in a voltage range of 0.5–2.9 V. A high discharge capacity of 515 mAh·g–1 was obtained after 400 cycles at 1 A·g–1, with a high initial columbic efficiency of 97.4%. Even at an ultrahigh rate of 35 A·g–1, a specific capacity of 128 mAh·g–1 was achieved. Using calculations, we revealed that the pseudocapacitance significantly contributed to the sodium-ion storage, especially at high current rates, leading to a high rate capability. The high comprehensive performance of the FeSe2 clusters makes them a promising anode material for SIBs.
Herein, hierarchically structured SnO2 microspheres are designed and synthesized as an efficient anode material for lithium-ion batteries using hollow SnO2 nanoplates. Three-dimensionally ordered macroporous (3-DOM) SnOx-C microspheres synthesized by spray pyrolysis are transformed into hierarchically structured SnO2 microspheres by a two-step post-treatment process. Sulfidation produces hierarchically structured SnS-SnS2-C microspheres comprising tin sulfide nanoplate and carbon building blocks. A subsequent oxidation process produces SnO2 microspheres from hollow SnO2 nanoplate building blocks, which are formed by Kirkendall diffusion. The discharge capacity of the hierarchically structured SnO2 microspheres at a current density of 5 A·g?1 for the 600th cycle is 404 mA·h·g?1. The hierarchically structured SnO2 microspheres have reversible discharge capacities of 609 and 158 mA·h·g?1 at current densities of 0.5 and 30 A·g?1, respectively. The ultrafine nanosheets contain empty voids that allow excellent lithium-ion storage performance, even at high current densities.
