Lithium metal has been regarded as the future anode material for high-energy-density rechargeable batteries due to its favorable combination of negative electrochemical potential and high theoretical ...capacity. However, uncontrolled lithium deposition during lithium plating/stripping results in low Coulombic efficiency and severe safety hazards. Herein, we report that nanodiamonds work as an electrolyte additive to co-deposit with lithium ions and produce dendrite-free lithium deposits. First-principles calculations indicate that lithium prefers to adsorb onto nanodiamond surfaces with a low diffusion energy barrier, leading to uniformly deposited lithium arrays. The uniform lithium deposition morphology renders enhanced electrochemical cycling performance. The nanodiamond-modified electrolyte can lead to a stable cycling of lithium | lithium symmetrical cells up to 150 and 200 h at 2.0 and 1.0 mA cm
, respectively. The nanodiamond co-deposition can significantly alter the lithium plating behavior, affording a promising route to suppress lithium dendrite growth in lithium metal-based batteries.Lithium metal is an ideal anode material for rechargeable batteries but suffer from the growth of lithium dendrites and low Coulombic efficiency. Here the authors show that nanodiamonds serve as an electrolyte additive to co-deposit with lithium metal and suppress the formation of dendrites.
The lithium (Li) metal anode is confronted by severe interfacial issues that strongly hinder its practical deployment. The unstable interfaces directly induce unfavorable low cycling efficiency, ...dendritic Li deposition, and even strong safety concerns. An advanced artificial protective layer with single‐ion pathways holds great promise for enabling a spatially homogeneous ionic and electric field distribution over Li metal surface, therefore well protecting the Li metal anode during long‐term working conditions. Herein, a robust dual‐phase artificial interface is constructed, where not only the single‐ion‐conducting nature, but also high mechanical rigidity and considerable deformability can be fulfilled simultaneously by the rational integration of a garnet Al‐doped Li6.75La3Zr1.75Ta0.25O12‐based bottom layer and a lithiated Nafion top layer. The as‐constructed artificial solid electrolyte interphase is demonstrated to significantly stabilize the repeated cell charging/discharging process via regulating a facile Li‐ion transport and a compact Li plating behavior, hence contributing to a higher coulombic efficiency and a considerably enhanced cyclability of lithium metal batteries. This work highlights the significance of rational manipulation of the interfacial properties of a working Li metal anode and affords fresh insights into achieving dendrite‐free Li deposition behavior in a working battery.
A single‐ion‐conducting interface consisting of dual‐layer architecture is proposed to regulate a homogeneous ionic and electric field distribution while achieving a superior mechanical feature at the surface of a lithium‐metal anode simultaneously, synergistically enabling a highly efficient cell performance of working lithium‐metal batteries.
Lithium (Li) metal has been pursued as “Holy Grail” among various anode materials due to its high specific capacity and the lowest reduction potential. However, uncontrolled growth of Li dendrites ...and extremely unstable interfaces during repeated Li plating/stripping ineluctably plague the practical applications of Li metal batteries. Herein, an artificial protective layer with synergistic soft–rigid feature is constructed on the Li metal anode to offer superior interfacial stability during long‐term cycles. By suppressing random Li deposition and the formation of isolated Li, such a protective layer enables a dendrite‐free morphology of Li metal anode and suppresses the depletion of Li metal and electrolyte. Additionally, sufficient ionic conductivity is guaranteed through the synergy between soft and rigid structural units that are uniformly dispersed in the layer. Dendrite‐free and dense Li deposition, as well as a greatly reduced interfacial resistance after cycling, is achieved owing to the stabilized interface, accounting for significantly prolonged cycle life of Li metal batteries. This work highlights the ability of synergistic organic/inorganic protective layer in stabilizing Li metal anode and provides fresh insights into the energy chemistry and mechanics of anode in a working battery.
An artificial protective layer based on the manipulation in the mechanical properties of soft–rigid and organic–inorganic hybrids is proposed for safe lithium metal anodes. The soft organic or polymeric materials offer stretchability to tolerate the volume fluctuation, while the rigid inorganic materials provide mechanical reinforcement and suppress the growth of lithium dendrites.
In recent years, the rapid development of modern society is calling for advanced energy storage to meet the growing demands of energy supply and generation. As one of the most promising energy ...storage systems, secondary batteries are attracting much attention. The electrolyte is an important part of the secondary battery, and its composition is closely related to the electrochemical performance of the secondary batteries. Lithium‐ion battery electrolyte is mainly composed of solvents, additives, and lithium salts, which are prepared according to specific proportions under certain conditions and according to the needs of characteristics. This review analyzes the advantages and current problems of the liquid electrolytes in lithium‐ion batteries (LIBs) from the mechanism of action and failure mechanism, summarizes the research progress of solvents, lithium salts, and additives, analyzes the future trends and requirements of lithium‐ion battery electrolytes, and points out the emerging opportunities in advanced lithium‐ion battery electrolytes development.
This review analyzes the advantages and current problems of the liquid electrolytes in lithium‐ion batteries from the mechanism of action and failure mechanism, summarizes the research progress of solvents, lithium salts, and additives, analyzes the future trends and requirements of lithium‐ion battery electrolytes, and points out the emerging opportunities in advanced lithium‐ion battery electrolytes development.
Lithium–sulfur (Li–S) batteries promise great potential as high‐energy‐density energy‐storage devices due to their ultrahigh theoretical energy density of 2600 Wh kg−1. Evaluation and analysis on ...practical Li–S pouch cells are essential for achieving actual high energy density under working conditions and affording developing directions for practical applications. This review aims to afford a comprehensive overview of high‐energy‐density Li–S pouch cells regarding 7 years of development and to point out further research directions. Key design parameters to achieve actual high energy density are addressed first, to define the research boundaries distinguished from coin‐cell‐level evaluation. Systematic analysis of the published literature and cutting‐edge performances is then conducted to demonstrate the achieved progress and the gap toward practical applications. Following that, failure analysis as well as promotion strategies at the pouch cell level are, respectively, discussed to reveal the unique working and failure mechanism that shall be accordingly addressed. Finally, perspectives toward high‐performance Li–S pouch cells are presented regarding the challenges and opportunities of this field.
High‐energy‐density lithium–sulfur pouch cells are cpomprehensively reviewed regarding the key design parameters, the current performances, and recent advances on failure analysis and promotion strategies on cathode, electrolyte, and anode.
Lithium–sulfur (Li–S) batteries have long been expected to be a promising high-energy-density secondary battery system since their first prototype in the 1960s. During the past decade, great progress ...has been achieved in promoting the performances of Li–S batteries by addressing the challenges at the laboratory-level model systems. With growing attention paid to the application of Li–S batteries, new challenges at practical cell scales emerge as the bottleneck. In this Outlook, the key parameters for practical Li–S batteries to achieve practical high energy density are emphasized regarding high-sulfur-loading cathodes, lean electrolytes, and limited excess anodes. Subsequently, the key scientific problems are redefined in practical Li–S batteries beyond the previous ones under ideal conditions. Finally, viable strategies are proposed to address the above challenges as future research directions.
In crop plants, a high-density genetic linkage map is essential for both genetic and genomic researches. The complexity and the large size of wheat genome have hampered the acquisition of a ...high-resolution genetic map. In this study, we report a high-density genetic map based on an individual mapping population using the Affymetrix Wheat660K single-nucleotide polymorphism (SNP) array as a probe in hexaploid wheat. The resultant genetic map consisted of 119 566 loci spanning 4424.4 cM, and 119 001 of those loci were SNP markers. This genetic map showed good collinearity with the 90 K and 820 K consensus genetic maps and was also in accordance with the recently released wheat whole genome assembly. The high-density wheat genetic map will provide a major resource for future genetic and genomic research in wheat. Moreover, a comparative genomics analysis among gramineous plant genomes was conducted based on the high-density wheat genetic map, providing an overview of the structural relationships among theses gramineous plant genomes. A major stable quantitative trait locus (QTL) for kernel number per spike was characterized, providing a solid foundation for the future high-resolution mapping and map-based cloning of the targeted QTL.
Lithium metal is among the most promising anode materials in next-generation energy-storage systems. However, Li dendrite growth and unstable solid electrolyte interphase have hindered its practical ...applications. Structured current collectors have been widely proposed to settle these issues, whereas the pre-filling of Li metal into structured anode is challenging. We proposed a coralloid silver-coated carbon fiber-based composite Li anode (CF/Ag-Li) through Ag electroplating and molten Li infusion. The molten Li can be infused into the carbon fiber framework due to the lithiophilic nature of Ag. In addition, a dendrite-free morphology and extraordinary electrochemical performance are achieved in Li-LiFePO4 and Li-sulfur cells. The CF/Ag-Li|Li symmetrical cells can cycle for 160 cycles at 10.0 mA cm−2 and 10.0 mAh cm−2. The CF/Ag-Li|S cells exhibited a high initial discharge capacity of 785 mAh g−1 and a large capacity retention rate after 400 cycles at 0.5C.
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•Coralloid carbon fibers were achieved by electroplating Ag onto their surface•Ag coating layer endows electrodes with lithiophilic nature to syphon molten Li•The composite Li electrode can cycle without dendrite growth or volume change•The composite Li can match Li-containing (LiFePO4) and Li-free (sulfur) cathodes
With the rapid development of electric vehicles and portable electronics such as mobile phones and laptops, the widely used lithium (Li)-ion batteries are having many difficulties in meeting the growing demands for high-energy-density energy-storage systems. Li metal, with an ultrahigh theoretical specific capacity of 3,860 mAh g−1 and the lowest negative electrochemical potential (−3.040 V versus standard hydrogen electrode), has become one of the most promising anode materials for next-generation batteries. Unfortunately, the practical application of Li metal anode has been hindered by its low cycling efficiency, short lifespan, and potential safety hazards. Herein we propose a Li-containing composite electrode based on coralloid carbon fibers that exhibited extraordinary electrochemical performance in full cells of Li-S and Li-LiFePO4 batteries. Such proof of concept on Li-infused structured electrodes sheds fresh light on the dendrite-free plating of Li metal anodes in working rechargeable batteries.
Lithium (Li) metal is among the most promising anode materials for next-generation high-energy-density batteries. However, both dendrite growth and unstable solid electrolyte interphases have hindered its practical applications. Herein, we propose a coralloid carbon fiber-based composite lithium anode, which is an initially Li-containing structured anode. Such electrode design renders dendrite-free morphology during repeated stripping/plating cycles and extraordinary electrochemical performance in Li-LiFePO4 and Li-sulfur cells.
Lithium (Li) metal anodes have attracted considerable interest due to their ultrahigh theoretical gravimetric capacity and very low redox potential. However, the issues of nonuniform lithium deposits ...(dendritic Li) during cycling are hindering the practical applications of Li metal batteries. Herein, we propose a concept of ion redistributors to eliminate dendrites by redistributing Li ions with Al-doped Li
La
Zr
Ta
O
(LLZTO) coated polypropylene (PP) separators. The LLZTO with three-dimensional ion channels can act as a redistributor to regulate the movement of Li ions, delivering a uniform Li ion distribution for dendrite-free Li deposition. The standard deviation of ion concentration beneath the LLZTO composite separator is 13 times less than that beneath the routine PP separator. A Coulombic efficiency larger than 98% over 450 cycles is achieved in a Li | Cu cell with the LLZTO-coated separator. This approach enables a high specific capacity of 140 mAh g
for LiFePO
| Li pouch cells and prolonged cycle life span of 800 hours for Li | Li pouch cells, respectively. This strategy is facile and efficient in regulating Li-ion deposition by separator modifications and is a universal method to protect alkali metal anodes in rechargeable batteries.
Lithium–sulfur (Li–S) batteries are regarded as promising high‐energy‐density energy storage devices. However, the cycling stability of Li–S batteries is restricted by the parasitic reactions between ...Li metal anodes and soluble lithium polysulfides (LiPSs). Encapsulating LiPS electrolyte (EPSE) can efficiently suppress the parasitic reactions but inevitably sacrifices the cathode sulfur redox kinetics. To address the above dilemma, a redox comediation strategy for EPSE is proposed to realize high‐energy‐density and long‐cycling Li–S batteries. Concretely, dimethyl diselenide (DMDSe) is employed as an efficient redox comediator to facilitate the sulfur redox kinetics in Li–S batteries with EPSE. DMDSe enhances the liquid–liquid and liquid–solid conversion kinetics of LiPS in EPSE while maintains the ability to alleviate the anode parasitic reactions from LiPSs. Consequently, a Li–S pouch cell with a high energy density of 359 Wh kg−1 at cell level and stable 37 cycles is realized. This work provides an effective redox comediation strategy for EPSE to simultaneously achieve high energy density and long cycling stability in Li–S batteries and inspires rational integration of multi‐strategies for practical working batteries.
A redox comediation strategy is proposed for promoting the cathode redox kinetics and simultaneously retaining the anode protection capability of lithium–sulfur batteries using encapsulating lithium polysulfide electrolyte. A 1.5 Ah lithium–sulfur pouch cell realizes a high initial energy density of 359 Wh kg−1 and 37 stable cycles following the above strategy.
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