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本文引用的文献

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Amorphous MoS as the sulfur-equivalent cathode material for room-temperature Li-S and Na-S batteries.非晶态 MoS 作为室温 Li-S 和 Na-S 电池的硫等效阴极材料。
Proc Natl Acad Sci U S A. 2017 Dec 12;114(50):13091-13096. doi: 10.1073/pnas.1711917114. Epub 2017 Nov 27.
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Interfacial Chemistry Regulation via a Skin-Grafting Strategy Enables High-Performance Lithium-Metal Batteries.通过皮接枝策略调节界面化学,实现高性能锂金属电池。
J Am Chem Soc. 2017 Nov 1;139(43):15288-15291. doi: 10.1021/jacs.7b06437. Epub 2017 Oct 10.
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Nanodiamonds suppress the growth of lithium dendrites.纳米金刚石抑制锂枝晶的生长。
Nat Commun. 2017 Aug 25;8(1):336. doi: 10.1038/s41467-017-00519-2.
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Electroless Formation of Hybrid Lithium Anodes for Fast Interfacial Ion Transport.用于快速界面离子输运的混合锂负极的化学镀法制备。
Angew Chem Int Ed Engl. 2017 Oct 9;56(42):13070-13077. doi: 10.1002/anie.201707754. Epub 2017 Sep 8.
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Toward Safe Lithium Metal Anode in Rechargeable Batteries: A Review.迈向可充电电池中安全的锂金属阳极:综述。
Chem Rev. 2017 Aug 9;117(15):10403-10473. doi: 10.1021/acs.chemrev.7b00115. Epub 2017 Jul 28.
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Protected Lithium-Metal Anodes in Batteries: From Liquid to Solid.电池中的受保护锂金属阳极:从液态到固态。
Adv Mater. 2017 Sep;29(36). doi: 10.1002/adma.201701169. Epub 2017 Jul 24.
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Functional metal-organic framework boosting lithium metal anode performance chemical interactions.功能性金属有机框架提升锂金属负极性能 化学相互作用
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Liquefied gas electrolytes for electrochemical energy storage devices.用于电化学储能装置的液化气体电解质。
Science. 2017 Jun 30;356(6345). doi: 10.1126/science.aal4263. Epub 2017 Jun 15.
9
Three-dimensional holey-graphene/niobia composite architectures for ultrahigh-rate energy storage.三维多孔石墨烯/铌酸复合材料用于超高倍率储能。
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High-capacity, low-tortuosity, and channel-guided lithium metal anode.高容量、低曲折度且具有通道导向的锂金属负极。
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基于深循环锂金属负极的高容量可充电电池。

High-capacity rechargeable batteries based on deeply cyclable lithium metal anodes.

机构信息

Department of Chemistry and Energy Sciences Institute, Yale University, West Haven, CT 06516.

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, 201620 Shanghai, People's Republic of China.

出版信息

Proc Natl Acad Sci U S A. 2018 May 29;115(22):5676-5680. doi: 10.1073/pnas.1803634115. Epub 2018 May 14.

DOI:10.1073/pnas.1803634115
PMID:29760091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5984539/
Abstract

Discovering new chemistry and materials to enable rechargeable batteries with higher capacity and energy density is of paramount importance. While Li metal is the ultimate choice of a battery anode, its low efficiency is still yet to be overcome. Many strategies have been developed to improve the reversibility and cycle life of Li metal electrodes. However, almost all of the results are limited to shallow cycling conditions (e.g., 1 mAh cm) and thus inefficient utilization (<1%). Here we achieve Li metal electrodes that can be deeply cycled at high capacities of 10 and 20 mAh cm with average Coulombic efficiency >98% in a commercial LiPF/carbonate electrolyte. The high performance is enabled by slow release of LiNO into the electrolyte and its subsequent decomposition to form a LiN and lithium oxynitrides (LiN O)-containing protective layer which renders reversible, dendrite-free, and highly dense Li metal deposition. Using the developed Li metal electrodes, we construct a Li-MoS full cell with the anode and cathode materials in a close-to-stoichiometric amount ratio. In terms of both capacity and energy, normalized to either the electrode area or the total mass of the electrode materials, our cell significantly outperforms other laboratory-scale battery cells as well as the state-of-the-art Li ion batteries on the market.

摘要

发现新的化学物质和材料,以实现具有更高容量和能量密度的可充电电池,这一点至关重要。尽管金属锂是电池阳极的最佳选择,但它的低效率仍有待克服。人们已经开发出许多策略来提高金属锂电极的可逆性和循环寿命。然而,几乎所有的结果都仅限于浅循环条件(例如,1 mAh cm),因此利用率不高(<1%)。在这里,我们实现了金属锂电极,在商用 LiPF/碳酸盐电解质中,在 10 和 20 mAh cm 的高容量下可以进行深度循环,平均库仑效率>98%。高性能是通过将 LiNO 缓慢释放到电解质中并随后分解形成含有 LiN 和锂氧氮化物(LiN O)的保护性层来实现的,该层使可逆、无枝晶且高度致密的金属锂沉积成为可能。使用开发的金属锂电极,我们构建了一个 Li-MoS 全电池,其阳极和阴极材料的比例接近化学计量比。就容量和能量而言,相对于电极面积或电极材料的总质量,我们的电池明显优于其他实验室规模的电池以及市场上的先进锂离子电池。