共查询到20条相似文献，搜索用时 10 毫秒
1.
Guochun Yan Kyle Reeves Dominique Foix Zhujie Li Claudio Cometto Sathiya Mariyappan Mathieu Salanne Jean‐Marie Tarascon 《Liver Transplantation》2019,9(41)
The Na‐ion battery is recognized as a possible alternative to the Li‐ion battery for applications where power and cost override energy density performance. However, the increasing instability of their electrolyte with temperature is still problematic. Thus, a central question remains how to design Na‐based electrolytes. Here, the discovery of a Na‐based electrolyte formulation is reported which enlists four additives (vinylene carbonate, succinonitrile, 1,3‐propane sultone, and sodium difluoro(oxalate)borate) in proper quantities that synergistically combine their positive attributes to enable a stable solid electrolyte interphase at both negative and positive electrodes surface at 55 °C. Moreover, the role of each additive that consists in producing specific NaF coatings, thin elastomers, sulfate‐based deposits, and so on via combined impedance and X‐ray photoelectron spectroscopy is rationalized. It is demonstrated that empirical electrolyte design rules previously established for Li‐ion technology together with theoretical guidance is vital in the quest for better Na‐based electrolytes that can be extended to other chemistries. Overall, this finding, which is implemented to 18 650 cells, widens the route to the rapid development of the Na‐ion technology based on Na3V2(PO4)2F3/C chemistry. 相似文献
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Julen Castillo Asier Soria-Fernández Sergio Rodriguez-Peña Jokin Rikarte Adrián Robles-Fernández Itziar Aldalur Rosalía Cid Jose Antonio González-Marcos Javier Carrasco Michel Armand Alexander Santiago Daniel Carriazo 《Liver Transplantation》2024,14(1):2302378
The growing requirements for electrified applications entail exploring alternative battery systems. Lithium-sulfur batteries (LSBs) have emerged as a promising, cost-effective, and sustainable solution; however, their practical commercialization is impeded by several intrinsic challenges. With the aim of surpassing these challenges, the implementation of a holistic LSB concept is proposed. To this end, the effectiveness of coupling a high-performing 2D graphene-based sulfur cathode with a well-suited sparingly solvating electrolyte (SSE) is reported. The incorporation of bis(fluorosulfonyl)imide (LiFSI) salt to tune sulfolane and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropylether based SSE enables the formation of a robust and compact lithium fluoride-rich solid electrolyte interphase. Consequently, the lithium compatibility is improved, achieving a high Coulombic efficiency (CE) of 98.8% in the Li||Cu cells and enabling thin and dense lithium depositions. When combined with a high-performing 2D graphene-based sulfur cathode, a symbiotic effect is shown, leading to high discharge capacities, remarkable rate capability (2.5 mAh cm−2 at C/2), enhanced cell stability, and wide temperature applicability. Furthermore, the scalability of this strategy is successfully demonstrated by assembling high-performing monolayer prototype cells with a total capacity of 93 mAh, notable capacity retention of 70% after 100 cycles, and a high average CE of 99%. 相似文献
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Ji Qian Feng Wu Yusheng Ye Menglu Zhang Yongxin Huang Yi Xing Wei Qu Li Li Renjie Chen 《Liver Transplantation》2018,8(16)
Sodium‐ion batteries (SIBs) are considered to be a promising alternative for large‐scale electricity storage. However, it is urgent to develop new anode materials with superior ultralong cycle life performance at high current rates. Herein, a low‐cost and large‐scalable sulfur‐doped carbon anode material that exhibits the best high‐rate cycle performance and the longest cycle life ever reported for carbon anodes is developed. The material delivers a reversible capacity of 142 mA h g?1 at a current rate up to 10 A g?1. After 10 000 cycles the capacity is remained at 126.5 mA h g?1; 89.1% of the initial value. Density functional theory computations demonstrate that the sulfur‐doped carbon has a strong binding affinity for sodium which promotes sodium storage. Meanwhile, the kinetics analysis identifies the capacitive charge storage as a large contributor to sodium storage, which favors ultrafast storage of sodium ions. These results demonstrate a new way to design carbon‐based SIBs anodes for next‐generation large‐scale electricity storage. 相似文献
4.
Dongjiang Chen Ziqi Zhou Chao Feng Weiqiang Lv Zhaohuan Wei Kelvin H. L. Zhang Bin Lin Songhao Wu Tianyu Lei Xuyun Guo Gaolong Zhu Xian Jian Jie Xiong Enrico Traversa Shi Xue Dou Weidong He 《Liver Transplantation》2019,9(15)
Structural/compositional characteristics at the anode/electrolyte interface are of paramount importance for the practical performance of lithium ion batteries, including cyclic stability, rate capacity, and operational safety. The anode‐electrolyte interface with traditional separator technology is featured with inevitable phase discontinuity and fails to support the stable operation of lithium ion batteries based on large‐capacity anodes with structural change in charges/discharges, such as transition metal oxide anodes. In this work, an anode/electrolyte framework based on an oxide anode and an active‐oxide‐incorporated separator is proposed for the first time and investigated for lithium ion batteries. The architecture builds a robust anode‐separator interface in LIBs, shortens Li+ diffusion path, accelerates electron transport, and mitigates the volume change of the oxide anode in electrochemical reactions. Remarkably, 4 wt% CuO addition in the separator leads to a 17% enhancement in the overall capacity of a battery with a CuO anode. The battery delivers an unparalleled record reversible capacity of 637.2 mAh g?1 with a 99% capacity retention after 100 charge/discharge cycles at 0.5 C. The high performance are attributed to the robust anode‐separator interface, which gives rise to enhanced interaction between the oxide anode and the same‐oxide‐incorporated composite in the separator. 相似文献
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Secondary batteries based on metal anodes (e.g., Li, Na, Mg, Zn, and Al) are among the most sought‐after candidates for next‐generation mobile and stationary storage systems because they are able to store a larger amount of energy per unit mass or volume. However, unstable electrodeposition and uncontrolled interfacial reactions occuring in liquid electrolytes cause unsatisfying cell performance and potential safety concerns for the commercial application of these metal anodes. Solid‐state electrolytes (SSEs) having a higher modulus are considered capable of inhibiting difficulties associated with the anodes and may enable building of safe all‐solid‐state metal batteries, yet several challenges, such as insufficient room‐temperature ionic conductivity and poor interfacial stability between the electrode and the electrolyte, hinder the large‐scale development of such batteries. Here, research and development of SSEs including inorganic ceramics, organic solid polymers, and organic–inorganic hybrid/composite materials for metal‐based batteries are reviewed. The comparison of different types of electrolytes is discussed in detail, in the context of electrochemical energy storage applications. Then, the focus of this study is on recent advances in a range of attractive and innovative battery chemistries and technologies that are enabled by SSEs. Finally, the challenges and future perspectives are outlined to foresee the development of SSEs. 相似文献
6.
Byeongyong Lee Myeongjin Kim Sunkyung Kim Jagjit Nanda Seok Joon Kwon Hee Dong Jang David Mitlin Seung Woo Lee 《Liver Transplantation》2020,10(17)
Structurally and chemically defective activated‐crumbled graphene (A‐CG) is employed to achieve unique synergy of large reversible potassium (K) and sodium (Na) ion storage capacity with fast charging and extended cyclability. A‐CG synthesis consists of low temperature spraying of graphene oxide slurry, followed by partial reduction annealing and air activation. For K storage, the reversible capacities are 340 mAh g?1 at 0.04 A g?1, 261 mAh g?1 at 0.5 A g?1, and 210 mAh g?1 at 2 A g?1. For Na storage, the reversible capacities are 280 mAh g?1 at 0.04 A g?1, 191 mAh g?1 at 0.5 A g?1, and 151 mAh g?1 at 2 A g?1. A‐CG shows a stable intermediate rate (0.5 Ag?1) cycling with both K and Na, with minimal fade after 2800 and 8000 cycles. These are among the most favorable capacity—rate capability—cyclability combinations recorded for potassium‐ion battery and sodium‐ion battery carbons. Electroanalytical studies (cyclic voltammetry, galvanostatic intermittent titration technique, b‐value) and density functional theory (DFT) reveal that enhanced electrochemical performance originates from ion adsorption at various defects, such as Stone–Wales defects. Moreover, DFT highlights enhanced thermodynamic stability of A‐CG with adsorbed K versus with adsorbed Na, explaining the unexpected higher reversible capacity with the former. 相似文献
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Binh Phuong Nhan Nguyen Nanjundan Ashok Kumar Joël Gaubicher Florence Duclairoir Thierry Brousse Olivier Crosnier Lionel Dubois Gérard Bidan Dominique Guyomard Bernard Lestriez 《Liver Transplantation》2013,3(10):1351-1357
Reduced graphene oxide (rGO) is used as a conductive additive for nanosilicon‐based lithium battery anodes with the high active‐mass loading typically required for industrial applications. In contrast to conventional Si electrodes that use acetylene black (AcB) as an additive, the rGO system shows pronounced improvement of electrochemical performance, irrespective of the cycling conditions. With capacity limitation, the rGO system results in improved coulombic efficiency (99.9%) and longer cycle life than conventional electrodes. Upon cycling without capacity limitation, much higher discharge capacity is maintained (2000 mAh g?1 after 100 cycles for 2.5 mg of Si cm?2). Used in conjunction with the bridging carboxymethyl cellulose binder, the crumpled and resilient rGO allows highly reversible functioning of the electrode in which the Si particles repeatedly inflate and deflate upon alloying and dealloying with lithium. 相似文献
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Guosheng Li Xiaochuan Lu Jin Y. Kim Vilayanur V. Viswanathan Kerry D. Meinhardt Mark H. Engelhard Vincent L. Sprenkle 《Liver Transplantation》2015,5(12)
Sodium‐metal chloride batteries, ZEBRA, are considered one of the most important electrochemical devices for stationary energy storage applications because of its advantages of good cycle life, safety, and reliability. However, sodium–nickel chloride (Na–NiCl2) batteries, the most promising redox chemistry in ZEBRA batteries, still face great challenges for the practical application due to its inevitable feature of using Ni cathode (high materials cost). Here, a novel intermediate‐temperature sodium–iron chloride (Na–FeCl2) battery using a molten sodium anode and Fe cathode is proposed and demonstrated. The first use of unique sulfur‐based additives in Fe cathode enables Na–FeCl2 batteries can be assembled in the discharged state and operated at intermediate temperature (<200 °C). The results presented demonstrate that intermediate‐temperature Na–FeCl2 battery technology could be a propitious solution for ZEBRA battery technologies by replacing the traditional Na–NiCl2 chemistry. 相似文献
10.
Development of high performance lithium‐ion (Li‐ion) power packs is a topic receiving significant attention in research today. Future development of the Li‐ion power packs relies on the development of high capacity and high rate anodes. More specifically, materials undergo either conversion or an alloying mechanism with Li. However, irreversible capacity loss (ICL) is one of the prime issues for this type of negative electrode. Traditional insertion‐type materials also experience ICL, but it is considered negligible. Therefore, eliminating ICL is crucial before the fabrication of practical Li‐ion cells with conventional cathodes such as LiFePO4, LiMn2O4, etc. There are numerous methods for eliminating ICL such as pre‐treating the electrode, usage of stabilized Li metal powder, chemical and electrochemical lithiation, sacrificial salts for both anode and cathode, etc. The research strategies that have been explored are reviewed here in regards to the elimination of ICL from the high capacity anodes as described. Additionally, mitigating ICL observed from the carbonaceous anodes is discussed and compared. 相似文献
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Seong‐Hyeon Choi Gyutae Nam Sujong Chae Donghyuk Kim Namhyung Kim Won Sik Kim Jiyoung Ma Jaekyung Sung Seung Min Han Minseong Ko Hyun‐Wook Lee Jaephil Cho 《Liver Transplantation》2019,9(4)
A significant volume expansion exhibited by high‐capacity active materials upon lithiation has hindered their application as Li‐ion battery anode materials. Although tremendous progress has been made in the development of coating methods that improve the stability of high‐capacity active materials, suitable coating sources that are both strong and economical to use are yet to be discovered. Pitch is reported here as a promising coating source for high‐capacity anodes owing to the high mechanical strength and low‐cost process. Using in situ transmission electron microscopy, it is found that pitch can withstand the severe volume expansion that occurs upon Si lithiation owing to its high mechanical strength, originating from the long‐range graphitic ordering. Notably, pitch‐coated silicon nanolayer–embedded graphite (SG) exhibits superior capacity retention (81.9%) compared to that of acetylene‐coated SG (66%) over 200 cycles in a full‐cell by effectively mitigating volume expansion, even under industrial electrode density conditions (1.6 g cc?1). Thus, this work presents new possibilities for the development of high‐capacity anodes for industrial implementation. 相似文献
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Developing high‐performance batteries through applying renewable resources is of great significance for meeting ever‐growing energy demands and sustainability requirements. Biomaterials have overwhelming advantages in material abundance, environmental benignity, low cost, and more importantly, multifunctionalities from structural and compositional diversity. Therefore, significant and fruitful research on exploiting various natural biomaterials (e.g., soy protein, chitosan, cellulose, fungus, etc.) for boosting high‐energy lithium‐based batteries by means of making or modifying critical battery components (e.g., electrode, electrolyte, and separator) are reported. In this review, the recent advances and main strategies for adopting biomaterials in electrode, electrolyte, and separator engineering for high‐energy lithium‐based batteries are comprehensively summarized. The contributions of biomaterials to stabilizing electrodes, capturing electrochemical intermediates, and protecting lithium metal anodes/enhancing battery safety are specifically emphasized. Furthermore, advantages and challenges of various strategies for fabricating battery materials via biomaterials are described. Finally, future perspectives and possible solutions for further development of biomaterials for high‐energy lithium‐based batteries are proposed. 相似文献
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Sodium (Na) metal, which possesses a high theoretical capacity and the lowest electrochemical potential, is regarded as a promising anode material for Na–metal batteries. However, both Na dendrite growth and large volume change in cycling have severely impeded its practical applications. This study demonstrates that a 3D flexible carbon (C) felt which is already commercialized in large‐scale can be employed as a host for prestoring Na via a melt infusion strategy, through which a Na/C composite anode is obtained. The resulting anode exhibits a stable voltage profile and a small hysteresis over 120 cycles in carbonate‐based electrolytes in symmetrical cells owing to the fact that the metallic Na is confined in a conductive carbon felt host, which increases the Na+ deposition sites to lower the effective current density and render a uniform Na nucleation, restricting the dimension change in electrochemical cycling. More importantly, effective inhibition of Na dendrite growth and large volume change is achieved. When coupled with a Na0.67Ni0.33Mn0.67O2 cathode, the Na/C composite demonstrates a good suitability in full cells. This work provides an alternative option for the fabrication of stable Na metal anodes, which is of great significance for the practical applications of Na metal anodes in high‐energy‐density batteries. 相似文献
18.
Wei Liu Yuting Xia Wenwu Wang Yizhe Wang Jialun Jin Yungui Chen Eunsu Paek David Mitlin 《Liver Transplantation》2019,9(3)
The role of graphene host structure/chemistry in plating–stripping in lithium metal anodes employed for lithium metal batteries is first examined in this study. Structural and chemical defects are bad, since highly defective graphene promotes unstable solid electrolyte interphase (SEI) growth. This consumes the fluoroethylene carbonate (FEC) additive in the carbonate electrolyte and is correlated with rapid decay in Coulombic efficiency (CE) and formation of filament‐like Li dendrites. A unique flow‐aided sonication exfoliation method is employed to synthesize “defect‐free” graphene (df‐G), allowing for a direct performance comparison with conventional reduced graphene oxide (r‐GO). At cycle 1, the r‐GO is better electrochemically wetted by Li than df‐G, indicating that initially it is more lithiophilic. With cycling, the nucleation overpotential with r‐GO becomes higher than with df‐G, indicating less facile plating reactions. The df‐G yields state‐of‐the‐art electrochemical performance, with the post cycled metal surface being relatively smooth and dendrite‐free. Conversely, r‐GO templates have CE rapidly degrade from the onset, with extensive dendrites after cycling. Severe SEI growth and associated FEC depletion with r‐GO are further confirmed by electrochemical impedance analysis and surface science methods. A new design rule is provided for Li metal templates: An ideal host must be noncatalytic toward SEI formation. 相似文献
19.
Fei Sun Hua Wang Zhibin Qu Kunfang Wang Lijie Wang Jihui Gao Jianmin Gao Shaoqin Liu Yunfeng Lu 《Liver Transplantation》2021,11(1):2002981
Oxygen-containing groups in carbon materials have been shown to affect the carbon anode performance of sodium ion batteries; however, precise identification of the correlation between specific oxygen specie and Na+ storage behavior still remains challenging as various oxygen groups coexist in the carbon framework. Herein, a postengineering method via a mechanochemistry process is developed to achieve accurate doping of (20.12 at%) carboxyl groups in a carbon framework. The constructed carbon anode delivers all-round improvements in Na+ storage properties in terms of a large reversible capacity (382 mAg−1 at 30 mA g−1), an excellent rate capability (153 mAg−1 at 2 A g−1) as well as good cycling stability (141 mAg−1 after 2000 cycles at 1.5 A g−1). Control experiments, kinetic analysis, density functional theory calculations, and operando measurements collectively demonstrate that carboxyl groups not only act as active sites for Na+ capacitive adsorption through suitable electrostatic interactions, but also gradually expand d-spacing by inducing a repulsive force between carbon layers with Na+ preadsorbed, and hence facilitate diffusion-controlled Na+ insertion process. This work provides a new insight in the rational tunning of oxygen-containing groups in carbon for boosting reversible Na+ storage through a synergy of adsorption and intercalation processes. 相似文献
20.
Shen Qiu Lifen Xiao Maria L. Sushko Kee Sung Han Yuyan Shao Mengyu Yan Xinmiao Liang Liqiang Mai Jiwen Feng Yuliang Cao Xinping Ai Hanxi Yang Jun Liu 《Liver Transplantation》2017,7(17)
Hard carbon is one of the most promising anode materials for sodium‐ion batteries, but the low Coulombic efficiency is still a key barrier. In this paper, a series of nanostructured hard carbon materials with controlled architectures is synthesized. Using a combination of in situ X‐ray diffraction mapping, ex situ nuclear magnetic resonance (NMR), electron paramagnetic resonance, electrochemical techniques, and simulations, an “adsorption–intercalation” mechanism is established for Na ion storage. During the initial stages of Na insertion, Na ions adsorb on the defect sites of hard carbon with a wide adsorption energy distribution, producing a sloping voltage profile. In the second stage, Na ions intercalate into graphitic layers with suitable spacing to form NaC x compounds similar to the Li ion intercalation process in graphite, producing a flat low voltage plateau. The cation intercalation with a flat voltage plateau should be enhanced and the sloping region should be avoided. Guided by this knowledge, nonporous hard carbon material has been developed which has achieved high reversible capacity and Coulombic efficiency to fulfill practical application. 相似文献