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1.
Transition metal sulfides, as an important class of inorganics, can be used as excellent electrode materials for various types of electrochemical energy storage, such as lithium‐ion batteries, sodium‐ion batteries, supercapacitors, and others. Recent works have identified that mixing graphene or graphene derivatives with transition metal sulfides can result in novel composites with better electrochemical performance. This review summarizes the latest advances in transition metal sulfide composites with graphene or graphene derivatives. The synthetic strategies and morphologies of these composites are introduced. The authors then discuss their applications in lithium‐ion batteries, sodium‐ion batteries, and supercapacitors. Finally, the authors give their personal viewpoints about the challenges and opportunities for the future development about this direction.  相似文献   

2.
Mixed metal sulfides (MMSs) have attracted increased attention as promising electrode materials for electrochemical energy storage and conversion systems including lithium‐ion batteries (LIBs), sodium‐ion batteries (SIBs), hybrid supercapacitors (HSCs), metal–air batteries (MABs), and water splitting. Compared with monometal sulfides, MMSs exhibit greatly enhanced electrochemical performance, which is largely originated from their higher electronic conductivity and richer redox reactions. In this review, recent progresses in the rational design and synthesis of diverse MMS‐based micro/nanostructures with controlled morphologies, sizes, and compositions for LIBs, SIBs, HSCs, MABs, and water splitting are summarized. In particular, nanostructuring, synthesis of nanocomposites with carbonaceous materials and fabrication of 3D MMS‐based electrodes are demonstrated to be three effective approaches for improving the electrochemical performance of MMS‐based electrode materials. Furthermore, some potential challenges as well as prospects are discussed to further advance the development of MMS‐based electrode materials for next‐generation electrochemical energy storage and conversion systems.  相似文献   

3.
Electrochemical energy storage is of extraordinary importance for fulfilling the utilization of renewable and sustainable energy sources. There is an increasing demand for energy storage devices with high energy and power densities, prolonged stability, safety, and low cost. In the past decade, numerous research efforts have been devoted to achieving these requirements, especially in the design of advanced electrode materials. Hollow carbon spheres (HCS) derived nanomaterials combining the advantages of 3D HCS and porous structures have been considered as alternative electrode materials for advanced energy storage applications, due to their unique features such as high surface‐to‐volume ratios, encapsulation capability, together with outstanding chemical and thermal stability. In this review, the authors first present a comprehensive overview of the synthetic strategies of HCS, and elucidate the design and synthesis of HCS‐derived nanomaterials including various types of HCS and their nanohybrids. Additionally, their significant roles as electrode materials for supercapacitors, lithium‐ion or sodium‐ion batteries, and sulfur hosts for lithium sulfur batteries are highlighted. Finally, current challenges in the synthesis of HCS and future directions in HCS‐derived nanomaterials for energy storage applications are proposed.  相似文献   

4.
Hollow and hierarchical nanostructures have received wide attention in new‐generation, high‐performance, lithium ion battery (LIB) applications. Both TiO2 and Fe2O3 are under current investigation because of their high structural stability (TiO2) and high capacity (Fe2O3), and their low cost. Here, we demonstrate a simple strategy for the fabrication of hierarchical hollow TiO2@Fe2O3 nanostructures for the application as LIB anodes. Using atomic layer deposition (ALD) and sacrificial template‐assisted hydrolysis, the resulting nanostructure combines a large surface area with a hollow interior and robust structure. As a result, such rationally designed LIB anodes exhibit a high reversible capacity (initial value 840 mAh g?1), improved cycle stability (530 mAh g?1 after 200 cycles at the current density of 200 mA g?1), as well as outstanding rate capability. This ALD‐assisted fabrication strategy can be extended to other hierarchical hollow metal oxide nanostructures for favorable applications in electrochemical and optoelectronic devices.  相似文献   

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6.
Featuring pronounced controllability, versatility, and scalability, electrophoretic deposition (EPD) has been proposed as an efficient method for film assembly and electrode/solid electrolyte fabrication in various energy storage/conversion devices including rechargeable batteries, supercapacitors, and fuel cells. High‐quality electrodes and solid electrolytes have been prepared through EPD and exhibit advantageous performances in comparison with those realized with traditional methods. Recent advances in the application of EPD materials in electrochemical energy storage and conversion devices are summarized. In particular, the parameters that influence the efficiency of an EPD process from colloidal preparation to deposition are evaluated with the aim to provide insightful guidance for realizing high‐performance electrochemical energy conversion materials and devices.  相似文献   

7.
In the past few years, insensitive attentions have been drawn to wearable and flexible energy storage devices/systems along with the emergence of wearable electronics. Much progress has been achieved in developing flexible electrochemical energy storage devices with high end‐use performance. However, challenges still remain in well balancing the electrochemical properties, mechanical properties, and the processing technologies. In this review, a specific perspective on the development of textile‐based electrochemical energy storage devices (TEESDs), in which textile components and technologies are utilized to enhance the energy storage ability and mechanical properties of wearable electronic devices, is provided. The discussion focuses on the material preparation and characteristics, electrode and device fabrication strategies, electrochemical performance and metrics, wearable compatibility, and fabrication scalability of TEESDs including textile‐based supercapacitors and lithium‐ion batteries.  相似文献   

8.
Lithium‐ion batteries (LIBs) with outstanding energy and power density have been extensively investigated in recent years, rendering them the most suitable energy storage technology for application in emerging markets such as electric vehicles and stationary storage. More recently, sodium, one of the most abundant elements on earth, exhibiting similar physicochemical properties as lithium, has been gaining increasing attention for the development of sodium‐ion batteries (SIBs) in order to address the concern about Li availability and cost—especially with regard to stationary applications for which size and volume of the battery are of less importance. Compared with traditional intercalation reactions, conversion reaction‐based transition metal oxides (TMOs) are prospective anode materials for rechargeable batteries thanks to their low cost and high gravimetric specific capacities. In this review, the recent progress and remaining challenges of conversion reactions for LIBs and SIBs are discussed, covering an overview about the different synthesis methods, morphological characteristics, as well as their electrochemical performance. Potential future research directions and a perspective toward the practical application of TMOs for electrochemical energy storage are also provided.  相似文献   

9.
Batteries have become fundamental building blocks for the mobility of modern society. Continuous development of novel battery chemistries and electrode materials has nourished progress in building better batteries. Simultaneously, novel device form factors and designs with multi‐functional components have been proposed, requiring batteries to not only integrate seamlessly to these devices, but to also be a multi‐functional component for a multitude of applications. Thus, in the past decade, along with developments in the component materials, the focus has been shifting more and more towards novel fabrication processes, unconventional configurations, and additional functionalities. This work attempts to critically review the developments with respect to emerging electrochemical energy storage configurations, including, amongst others, paintable, transparent, flexible, wire or cable shaped, ultra‐thin and ultra‐thick configurations, as well as hybrid energy storage‐conversion, or graphene‐incorporated batteries and supercapacitors. The performance requirements are elaborated together with the advantages, but also the limitations, with respect to established electrochemical energy storage technologies. Finally, challenges in developing novel materials with tailored properties that would allow such configurations, and in designing easier manufacturing techniques that can be widely adopted are considered.  相似文献   

10.
Energy storage devices are arousing increasing interest due to their key role in next‐generation electronics. Integration is widely explored as a general and effective strategy aiming at high performances. Recent progress in integrating a variety of functions into electrochemical energy storage devices is carefully described. Through integration at the level of materials: flexible, stretchable, responsive, and self‐healing devices are discussed to highlight the state‐of‐the‐art multi‐functional electronics. Through the integration at the level of devices, the incorporation of photovoltaic and piezoelectric devices is detailed to reflect the advances in self‐powering electronics. Integrated energy storage devices are presented for wearable applications to indicate a new growth direction. The main challenges and important directions are summarized to offer some useful clues for future development.  相似文献   

11.
Among the different nanostructures that have been demonstrated as promising materials for various applications, 3D nanostructures have attracted significant attention as building blocks for constructing high‐performance nanodevices. Particularly over the last decade, considerable research efforts have been devoted to designing, fabricating, and evaluating 3D nanostructures as electrodes for electrochemical energy conversion and storage devices. Although remarkable progress has been achieved, the performance of electrochemical energy devices based on 3D nanostructures in terms of energy conversion efficiency, energy storage capability, and device reliability still needs to be significantly improved to meet the requirements for practical applications. Rather than simply outlining and comparing different 3D nanostructures, this article systematically summarizes the general advantages as well as the existing and future challenges of 3D nanostructures for electrochemical energy conversion and storage, focusing on photoelectrochemical water splitting, photoelectrocatalytic solar‐to‐fuels conversion from nitrogen and carbon dioxide, rechargeable metal‐ion batteries, and supercapacitors. A comprehensive understanding of these advantages and challenges shall provide valuable guidelines and enlightenments to facilitate the further development of 3D nanostructured materials, and contribute to the achieving more efficient energy conversion and storage technologies toward a sustainable energy future.  相似文献   

12.
13.
The increasing demands for integration of renewable energy into the grid and urgently needed devices for peak shaving and power rating of the grid both call for low‐cost and large‐scale energy storage technologies. The use of secondary batteries is considered one of the most effective approaches to solving the intermittency of renewables and smoothing the power fluctuations of the grid. In these batteries, the states of the electrode highly affect the performance and manufacturing process of the battery, and therefore leverage the price of the battery. A battery with liquid metal electrodes is easy to scale up and has a low cost and long cycle life. In this progress report, the state‐of‐the‐art overview of liquid metal electrodes (LMEs) in batteries is reviewed, including the LMEs in liquid metal batteries (LMBs) and the liquid sodium electrode in sodium‐sulfur (Na–S) and ZEBRA (Na–NiCl2) batteries. Besides the LMEs, the development of electrolytes for LMEs and the challenge of using LMEs in the batteries, and the future prospects of using LMEs are also discussed.  相似文献   

14.
Transition‐metal (Fe, Co, Ni) based metal‐organic framework materials with controllable structures, large surface areas and adjustable pore sizes have attracted wide research interest for use in next‐generation electrochemical energy‐storage devices. This review introduces the synthesis of transition‐metal (Fe, Co, Ni) based metal‐organic frameworks and their derivatives with the focus on their application in supercapacitors and batteries.  相似文献   

15.
The ion insertion properties of MoS2 continue to be of widespread interest for energy storage. While much of the current work on MoS2 has been focused on the high capacity four‐electron reduction reaction, this process is prone to poor reversibility. Traditional ion intercalation reactions are highlighted and it is demonstrated that ordered mesoporous thin films of MoS2 can be utilized as a pseudocapacitive energy storage material with a specific capacity of 173 mAh g?1 for Li‐ions and 118 mAh g?1 for Na‐ions at 1 mV s?1. Utilizing synchrotron grazing incidence X‐ray diffraction techniques, fast electrochemical kinetics are correlated with the ordered porous structure and with an iso‐oriented crystal structure. When Li‐ions are utilized, the material can be charged and discharged in 20 seconds while still achieving a specific capacity of 140 mAh g?1. Moreover, the nanoscale architecture of mesoporous MoS2 retains this level of lithium capacity for 10 000 cycles. A detailed electrochemical kinetic analysis indicates that energy storage for both ions in MoS2 is due to a pseudocapacitive mechanism.  相似文献   

16.
This study presents a battery concept with a “mediator‐ion” solid electrolyte for the development of next‐generation electrochemical energy storage technologies. The active anode and cathode materials in a single cell can be in the solid, liquid, or gaseous form, which are separated by a sodium‐ion solid‐electrolyte separator. The uniqueness of this mediator‐ion strategy is that the redox reactions at the anode and the cathode are sustained by a shuttling of a mediator sodium ion between the anolyte and the catholyte through the solid‐state electrolyte. Use of the solid‐electrolyte separator circumvents the chemical‐crossover problem between the anode and the cathode, overcomes the dendrite‐problem when employing metal‐anodes, and offers the possibility of using different liquid electrolytes at the anode and the cathode in a single cell. The battery concept is demonstrated with two low‐cost metal anodes (zinc and iron), two liquid cathodes (bromine and potassium ferricyanide), and one gaseous cathode (air/O2) with a sodium‐ion solid electrolyte. This novel battery strategy with a mediator‐ion solid electrolyte is applicable to a wide range of electrochemical energy storage systems with a variety of cathodes, anodes, and mediator‐ion solid electrolytes.  相似文献   

17.
The high demand for clean and renewable energy has fueled the exploration of advanced energy storage systems. As a potential alternative device for lithium ion batteries, sodium ion batteries (NIBs) have attracted extraordinary attention and are becoming a promising candidate for energy storage due to their low cost and high efficiency. Recent progress has demonstrated that metal sulfides (MSs) are very promising electrode candidates for efficient Na‐storage devices, because of their excellent redox reversibility and relatively high capacity. In this review, recent developments of MSs as anode materials for NIBs are presented. The corresponding electrochemical mechanisms are briefly discussed. We also present critical issues, challenges, and perspectives with the hope of providing a fuller understanding of the associated electrochemical processes. Such an understanding is critical for tailoring and designing metal sulfides with the desired activity and stability.  相似文献   

18.
Hard carbon has long been considered the leading candidate for anode materials of Na‐ion batteries. Intensive research efforts have been carried out in the search of suitable carbon structure for an improved storage capability. Herein, an anode based on multishelled hollow carbon nanospheres, which are able to deliver an outstanding electrochemical performance with an extraordinary reversible capacity of 360 mAh g?1 at 30 mA g?1, is designed. An interesting dependence of the electrochemical properties on the multishelled structural features is identified: with an increase in the shell number of the model carbon materials, the sloping capacity in the charge/discharge curve remains almost unchanged while the plateau capacity continuously increases, suggesting an adsorption‐filling Na‐storage mechanism for the multishelled hollow hard carbon materials. The findings not only provide new perspective in the structural design of high‐performance anode materials, but also shed light on the complicated mechanism behind Na‐storage by hard carbon.  相似文献   

19.
With the booming development of flexible and wearable electronics, their safety issues and operation stabilities have attracted worldwide attentions. Compared with traditional liquid electrolytes, gel polymer electrolytes (GPEs) are preferred due to their higher safety and adaptability to the design of flexible energy storage devices. This review summarizes the recent progress of GPEs with enhanced physicochemical properties and specified functionalities for the application in electrochemical energy storage. Functional GPEs that are capable to achieve unity lithium‐ion transference number and offer additional pseudocapacitance to the overall capacitance are carefully discussed. The smart GPEs with self‐protection, thermotolerant, and self‐healing abilities are particularly highlighted. To close, the future directions and remaining challenges of the GPEs for application in electrochemical energy storages are summarized to provide clues for the following development.  相似文献   

20.
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