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1.
    
An overview of fast charging materials for high power applications is given. The behavior at high current density of several anodic and cathodic materials that have been utilized in lithium‐, sodium‐, and potassium‐ion batteries is considered. Furthermore, the behavior of capacitive and pseudocapacitive materials suitable for electrochemical capacitors and, also, of those that have been utilized for the realization of hybrid‐ion capacitors, which are nowadays an interesting reality in the field of high power devices, is discussed. The advantages and limitations of all these materials are critically analyzed with the aim of understanding their impact on real devices. On the basis of this analysis, the most important aspects are identified, which should be addressed in the future for the realization of advanced high power devices.  相似文献   

2.
    
A rationally designed “air chargeable” energy storage device is demonstrated, which can be effectively charged by harvesting pervasive energy from the ambient environment. For an “air chargeable” zinc‐ion capacitor system, the system simply consists of a flexible bifunctional “U” shaped electrode (with the functions of energy harvesting and storage), a zinc metal electrode in middle, and two different polyelectrolytes (polyacrylamide and sodium polyacrylate) sandwiched between the zinc metal and “U” shaped electrode. When the zinc‐ion capacitor is exhausted, it can be quickly charged to 88% within 10 min by simply opening the sealing tape and allowing the air diffuse in. The capacitor exhausting‐air charging processes are repeated 60 times and the whole system works well. When the external power supplier is available, both the zinc‐ion capacitor and “air charging” component can be fully recovered. A large capacity (≈1000 mAh) “air chargeable” zinc‐vanadium battery is also demonstrated. The zinc‐vanadium battery can be fully charged by air in 1 h. This work offers a usage scenario independent reliable self‐chargeable power supply system as a promising approach to solve the intermittent and unpredictable nature of currently developed self‐chargeable devices.  相似文献   

3.
    
The reliability and durability of lithium‐ion capacitors (LICs) are severely hindered by the kinetic imbalance between capacitive and Faradaic electrodes. Efficient charge storage in LICs is still a huge challenge, particularly for thick electrodes with high mass loading, fast charge delivery, and harsh working conditions. Here, a unique thermally durable, stable LIC with high energy density from all‐inorganic hydroxyapatite nanowire (HAP NW)‐enabled electrodes and separators is reported. Namely, the LIC device is designed and constructed with the electron/ion dual highly conductive and fire‐resistant composite Li4Ti5O12‐based anode and activated carbon‐based cathode, together with a thermal‐tolerant HAP NW separator. Despite the thick‐electrode configuration, the as‐fabricated all HAP NW‐enabled LIC exhibits much enhanced electrochemical kinetics and performance, especially at high current rates and temperatures. Long cycling lifetime and state‐of‐the‐art areal energy density (1.58 mWh cm?2) at a high mass loading of 30 mg cm?2 are achieved. Benefiting from the excellent fire resistance of HAP NWs, such an unusual LIC exhibits high thermal durability and can work over a wide range of temperatures from room temperature to 150 °C. Taking full advantage of synergistic configuration design, this work sets the stage for designing advanced LICs beyond the research of active materials.  相似文献   

4.
    
High energy density at high power density is still a challenge for the current Li‐ion capacitors (LICs) due to the mismatch of charge‐storage capacity and electrode kinetics between capacitor‐type cathode and battery‐type anode. In this work, B and N dual‐doped 3D porous carbon nanofibers are prepared through a facile method as both capacitor‐type cathode and battery‐type anode for LICs. The B and N dual doping has profound effect in tuning the porosity, functional groups, and electrical conductivity for the porous carbon nanofibers. With rational design, the developed B and N dual‐doped carbon nanofibers (BNC) exhibit greatly improved electrochemical performance as both cathode and anode for LICs, which greatly alleviates the mismatch between the two electrodes. For the first time, a 4.5 V “dual carbon” BNC//BNC LIC device is constructed and demonstrated, exhibiting outstanding energy density and power capability compared to previously reported LICs with other configurations. In specific, the present BNC//BNC LIC device can deliver a large energy density of 220 W h kg?1 and a high power density of 22.5 kW kg?1 (at 104 W h kg?1) with reasonably good cycling stability (≈81% retention after 5000 cycles).  相似文献   

5.
    
Sodium‐based energy storage technologies are potential candidates for large‐scale grid applications owing to the earth abundance and low cost of sodium resources. Transition metal phosphides, e.g. MoP, are promising anode materials for sodium‐ion storage, while their detailed reaction mechanisms remain largely unexplored. Herein, the sodium‐ion storage mechanism of hexagonal MoP is systematically investigated through experimental characterizations, density functional theory calculations, and kinetics analysis. Briefly, it is found that the naturally covered surface amorphous molybdenum oxides layers on the MoP grains undergo a faradaic redox reaction during sodiation and desodiation, while the inner crystalline MoP remains unchanged. Remarkably, the MoP anode exhibits a pseudocapacitive‐dominated behavior, enabling the high‐rate sodium storage performance. By coupling the pseudocapacitive anode with a high‐rate‐battery‐type Na3V2O2(PO4)2F@rGO cathode, a novel sodium‐ion full cell delivers a high energy density of 157 Wh kg?1 at 97 W kg?1 and even 52 Wh kg?1 at 9316 W kg?1. These findings present the deep understanding of the sodium‐ion storage mechanism in hexagonal MoP and offer a potential route for the design of high‐rate sodium‐ion storage materials and devices.  相似文献   

6.
    
Sodium‐ion capacitors (SICs) can effectively combine high energy density with high power density, and are especially appropriate for high‐power demanding applications of large‐scale stationary energy storage. Surface‐induced pseudocapacitive charge storage based on porous or nano carbon materials is regarded as the most promising candidate for SICs. Unfortunately, their ultralow packing densities severely restrict their practical applications. A novel approach toward ultrafast high‐volumetric SICs based on folded‐graphene electrodes has already been demonstrated and showed quite competitive performance. In this work, it is further proved that oxygen functional groups and folded texture are two key elements for high‐volumetric sodium storage of folded‐graphene electrodes. Through a simple and controllable method, of thermal treatment in inert atmosphere, both the oxygen functional groups and folded texture can be quantitatively manipulated to better investigate the individual contribution and mutual interplay. It is illustrated that oxygen functional groups are crucial to superior capacitive sodium storage while folded texture is not only the origin for high‐volumetric sodium storage but also beneficial for both capacitive and additional diffusion‐controlled sodium storage. Inspired by above‐mentioned conclusion, more rational designs and effective preparation of advanced structure and novel materials can be realized to better promote the development of high‐volumetric SICs.  相似文献   

7.
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8.
    
Phosphorene, monolayer or few‐layer black phosphorus (BP), has recently triggered strong scientific interest for lithium/sodium ion batteries (LIBs/SIBs) applications. However, there are still challenges regarding large‐scale fabrication, poor air stability. Herein, we report the high‐yield synthesis of phosphorene with good crystallinity and tunable size distributions via liquid‐phase exfoliation of bulk BP in formamide. Afterwards, a densely packed phosphorene–graphene composite (PG‐SPS, a packing density of 0.6 g cm?3) is prepared by a simple and easily up‐scalable spark plasma sintering (SPS) process. When working as anode materials of LIBs, PG‐SPS exhibit much improved first‐cycle Coloumbic efficiency (60.2%) compared to phosphorene (11.5%) and loosely stacked phosphorene–graphene composite (34.3%), high specific capacity (1306.7 mAh g?1) and volumetric capacity (256.4 mAh cm?3), good rate capabilities (e.g., 415.0 mAh g?1 at 10 A g?1) as well as outstanding long‐term cycling life (91.9% retention after 800 cycles at 10 A g?1). Importantly, excellent air stability of PG‐SPS over the 60 days observation in maintaining its high Li storage properties can be achieved. On the contrary, 95.2% of BP in PG sample was oxidized after only 10 days exposure to ambience, leading to severe degradation of electrochemical properties.  相似文献   

9.
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10.
    
Na‐ion capacitors have attracted extensive interest due to the combination of the merits of high energy density of batteries and high power density as well as long cycle life of capacitors. Here, a novel Na‐ion capacitor, utilizing TiO2@CNT@C nanorods as an intercalation‐type anode and biomass‐derived carbon with high surface area as an ion adsorption cathode in an organic electrolyte, is reported. The advanced architecture of TiO2@CNT@C nanorods, prepared by electrospinning method, demonstrates excellent cyclic stability and outstanding rate capability in half cells. The contribution of extrinsic pseudocapacitance affects the rate capability to a large extent, which is identified by kinetics analysis. A key finding is that ion/electron transfer dynamics of TiO2@CNT@C could be effectively enhanced due to the addition of multiwalled carbon nanotubes. Also, the biomass‐derived carbon with high surface area displays high specific capacity and excellent rate capability. Owing to the merits of structures and excellent performances of both anode and cathode materials, the assembled Na‐ion capacitors provide an exceptionally high energy density (81.2 W h kg?1) and high power density (12 400 W kg?1) within 1.0–4.0 V. Meanwhile, the Na‐ion capacitors achieve 85.3% capacity retention after 5000 cycles tested at 1 A g?1.  相似文献   

11.
    
Spinel‐layered composites, where a high‐voltage spinel is incorporated in a layered lithium‐rich (Li‐rich) cathode material with a nominal composition x{0.6Li2MnO3 · 0.4[LiCo0.333Mn0.333Ni0.333]O2} · (1 – x) Li[Ni0.5Mn1.5]O4 (x = 0, 0.3, 0.5, 0.7, 1) are synthesized via a hydroxide assisted coprecipitation route to generate high‐energy, high‐power cathode materials for Li‐ion batteries. X‐ray diffraction patterns and the cyclic voltammetry investigations confirm the presence of both the parent components in the composites. The electrochemical investigations performed within a wide potential window show an increased structural stability of the spinel component when incorporated into the composite environment. All the composite materials exhibit initial discharge capacities >200 mAh g–1. The compositions with x = 0.5 and 0.7 show excellent cycling stability among the investigated materials. Moreover, the first cycle Coulombic efficiency achieve a dramatic improvement with the incorporation of the spinel component. More notably, the composite materials with increased spinel component exhibit superior rate capability compared with the parent Li‐rich material especially together with the highest capacity retention for x = 0.5 composition, making this as the optimal high‐energy high‐power material. The mechanisms involved in the symbiotic relationship of the spinel and layered Li‐rich components in the above composites are discussed.  相似文献   

12.
    
Ongoing interest is focused on aqueous zinc ion batteries (ZIBs) for mass‐production energy storage systems as a result of their affordability, safety, and high energy density. Ensuring the stability of the electrode/electrolyte interface is of particular importance for prolonging the cycling ability to meet the practical requirements of rechargeable batteries. Zinc anodes exhibit poor cycle life and low coulombic efficiency, stemming from the severe dendrite growth, and irreversible byproducts such as H2 and inactive ZnO. Great efforts have recently been devoted to zinc anode protection for designing high‐performance ZIBs. However, the intrinsic origins of zinc plating/striping are poorly understood, which greatly delay its potential applications. Rather than focusing on battery metrics, this review delves deeply into the underlying science that triggers the deposition/dissolution of zinc ions. Furthermore, recent advances in modulating the zinc coordination environment, uniforming interfacial electric fields, and inducing zinc deposition are highlighted and summarized. Finally, perspectives and suggestions are provided for designing highly stable zinc anodes for the industrialization of the aqueous rechargeable ZIBs in the near future.  相似文献   

13.
    
3D batteries continue to be of widespread interest for flexible energy storage where the 3D nanostructured cathode is the key component to achieve both high energy and power densities. While current work on flexible cathodes tends to emphasize the use of flexible scaffolds such as graphene and/or carbon nanotubes, this approach is often limited by poor electrical contact and structural stability. This communication presents a novel synthetic approach to form 3D array cathode for the first time, the single‐crystalline Na3(VO)2(PO4)2F (NVOPF) by using VO2 array as a seed layer. The NVOPF cathode exhibits both high‐rate capability (charge/discharge in 60 s) and long‐term durability (10,000 cycles at 50 C) for Na ion storage. Utilizing in situ X‐ray diffraction and first principles calculations, the high‐rate properties are correlated with the small volume change, 2D fast ion transport, and the array morphology. A novel all‐array flexible Na+ hybrid energy storage device based on pairing the intercalation‐type NVOPF array cathode with a cogenetic pseudocapacitive VO2 nanosheet array anode is demonstrated.  相似文献   

14.
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15.
    
Interface engineering is of great concern in photovoltaic devices. For the solution‐processed perovskite solar cells, the modification of the bottom surface of the perovskite layer is a challenge due to solvent incompatibility. Herein, a Cl‐containing tin‐based electron transport layer; SnOx‐Cl, is designed to realize an in situ, spontaneous ion‐exchange reaction at the interface of SnOx‐Cl/MAPbI3. The interfacial ion rearrangement not only effectively passivates the physical contact defects, but, at the same time, the diffusion of Cl ions in the perovskite film also causes longitudinal grain growth and further reduces the grain boundary density. As a result, an efficiency of 20.32% is achieved with an extremely high open‐circuit voltage of 1.19 V. This versatile design of the underlying carrier transport layer provides a new way to improve the performance of perovskite solar cells and other optoelectronic devices.  相似文献   

16.
    
Lithium‐ion hybrid supercapacitors (LICs) are considered as a promising candidate in energy storage systems. Taking the factor of sluggish kinetics behavior, battery‐type anode plays a significant role in improving the performance of LICs. Here, onion‐shaped graphene‐like derivatives are synthesized via carbonization of metalorganic quantum dots (MQDs) accompanied with in situ catalytic graphitization by reduced metal. Notably MQDs, exhibiting water‐soluble character and ultrafine particles (2.5–5.5 nm) morphology, are prepared by the amidation reaction. The carbonized sample exhibits highly graphitic tendency with graphitization degree up to 95.6%, and shows graphene‐like porous structure, appropriate amorphous carbon decoration characteristic, as well as N‐doping and defective nature. When employed as anode material in LICs, it shows high energy density of 83.7 Wh kg–1 and high power density of 6527 W kg–1 when the mass ratio of cathode to anode is 1:1 and the operating voltage ranges from 2.0 to 4.0 V. It also possesses the long cyclic stability with the energy density retention maintains at 97.3% after 10 000 cycles at 5.0 A g–1. In addition, the energy density is further increased by altering cathode/anode mass ratio and extending working voltage. This work provides a novel strategy to develop unique carbon materials for energy storage.  相似文献   

17.
    
Design and synthesis of metal oxide‐based pseudocapacitive materials to simultaneously achieve high mass loading (e.g., up to 10 mg cm?2) and excellent rate capability for electrochemical capacitors is a long‐lasting challenge. These two characteristics are usually mutually exclusive due to the poor ion diffusion kinetics of most metal oxides. Here, a glucose‐assisted hydrothermal method to prepare thick hematite film (>1 µm) with engineerable mesopore size through controlled variation of glucose concentration is demonstrated. The capability of controlling the size of mesopores offers a unique opportunity to investigate for the first time the interplay between mesopore size and electrochemical performance of hematite films. The hematite film with an average mesopore size of 3 nm at an ultrahigh loading of 10 mg cm?2 exhibits an areal capacitance of 1502 mF cm?2 at 1 mA cm?2, and retains 871.2 mF cm?2 at 50 mA cm?2. Such performance, to the best of the authors' knowledge, is at the top of the reported hematite electrodes with comparable or even lower mass loadings. The strategy demonstrated herein may be extended to fabricate diverse types of mesoporous metal oxide architectures with improved ion diffusion kinetics, which is critical for a broad range of devices for energy storage and conversion.  相似文献   

18.
    
The rapid development of smart wearable and integrated electronic products has urgently increased the requirement for high‐performance microbatteries. Although few lithium ion microbatteries based on organic electrolytes have been reported so far, the problems, such as undesirable energy density, poor flexibility, inflammability, volatility toxicity, and high cost restrict their practical applications in the above‐mentioned electronic products. In order to overcome these problems, a low cost quasi‐solid‐state aqueous zinc ion microbattery (ZIMB) assembled by a vanadium dioxide (B)‐multiwalled carbon nanotubes (VO2 (B)‐MWCNTs) cathode, a zinc nanoflakes anode, and a zinc trifluoromethanesulfonate‐polyvinyl alcohol (Zn(CF3SO3)2‐PVA) hydrogel electrolyte is exploited. As expected, the ZIMB exhibits excellent electrochemical performance, e.g., a high capacity of 314.7 µAh cm?2, an ultrahigh energy density of 188.8 µWh cm?2, and a high power density of 0.61 mW cm?2. Furthermore, the ZIMB also shows high flexibility and excellent high temperature stability: the capacity has no obvious decay when the bending angle is up to 150° and the temperature reaches 100 °C. The ZIMB provides a way to develop next‐generation miniature energy storage devices with high performance.  相似文献   

19.
    
Room‐temperature rechargeable sodium‐ion batteries are considered as a promising alternative technology for grid and other storage applications due to their competitive cost benefit and sustainable resource supply, triumphing other battery systems on the market. To facilitate the practical realization of the sodium‐ion technology, the energy density of sodium‐ion batteries needs to be boosted to the level of current commercial Li‐ion batteries. An effective approach would be to elevate the operating voltage of the battery, which requires the use of electrochemically stable cathode materials with high voltage versus Na+/Na. This review summarizes the recent progress with the emerging high‐voltage cathode materials for room‐temperature sodium‐ion batteries, which include layered transitional‐metal oxides, Na‐rich materials, and polyanion compounds. The key challenges and corresponding strategies for these materials are also discussed, with an emphasis placed on the intrinsic structural properties, Na storage electrochemistry, and the voltage variation tendency with respect to the redox reactions. The insights presented in this article can serve as a guide for improving the energy densities of room‐temperature Na‐ion batteries.  相似文献   

20.
    
The volume expansion and dendrite growth of metallic Li anode during charge/discharge processes hinder its practical application in energy storage. Seeking an appropriate host for distributing bulk Li in a 3D manner is an effective way to solve these problems. Here, a novel porous graphene scaffold with cellular chambers for incorporating Li metal is presented. Using such a unique host, ultrathin Li layers of 3 µm in thickness are anchored on graphene to form porous microstructures, which provides much more reaction sites for Li ions compared with that of bulk Li, significantly promoting the reversibility of Li stripping and plating. Also the high current density can be effectively dissipated by the graphene scaffold to remarkably improve the rate capability of Li anode. The symmetrical Li cell using such a Li anode can run stably for 200 cycles at 5 mA cm?2 and even 70 cycles at 10 mA cm?2 in an unmodified carbonate‐based electrolyte, which has rarely been achieved in such aggressive working conditions. Lithium‐ion capacitor cells using this anode also show outstanding rate capability and cycling stability, which can work at an ultrahigh current density of 30 A g?1 and keep steady for over 4000 cycles at 3.75 A g?1.  相似文献   

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