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锂离子电池中具有超快和稳定循环性能的钛酸锂水合物。

Lithium titanate hydrates with superfast and stable cycling in lithium ion batteries.

机构信息

State Key Lab of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, 100084, China.

Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, 02139, USA.

出版信息

Nat Commun. 2017 Sep 20;8(1):627. doi: 10.1038/s41467-017-00574-9.

Abstract

Lithium titanate and titanium dioxide are two best-known high-performance electrodes that can cycle around 10,000 times in aprotic lithium ion electrolytes. Here we show there exists more lithium titanate hydrates with superfast and stable cycling. That is, water promotes structural diversity and nanostructuring of compounds, but does not necessarily degrade electrochemical cycling stability or performance in aprotic electrolytes. As a lithium ion battery anode, our multi-phase lithium titanate hydrates show a specific capacity of about 130 mA h g at ~35 C (fully charged within ~100 s) and sustain more than 10,000 cycles with capacity fade of only 0.001% per cycle. In situ synchrotron diffraction reveals no 2-phase transformations, but a single solid-solution behavior during battery cycling. So instead of just a nanostructured intermediate to be calcined, lithium titanate hydrates can be the desirable final destination.Water is usually not favorable in high-voltage window aprotic electrolytes. Here the authors discover some lithium titanate hydrates that allow superior power rate and ultralong cycle life in aprotic electrolytes.

摘要

钛酸锂和二氧化钛是两种最知名的高性能电极,它们在非质子锂离子电解液中可以循环 10000 次左右。在这里,我们展示了存在更多具有超快和稳定循环性能的钛酸锂水合物。也就是说,水促进了化合物的结构多样性和纳米结构,但不一定会降低非质子电解液中电化学循环的稳定性或性能。作为锂离子电池的阳极,我们的多相钛酸锂水合物在35°C 时的比容量约为 130 mA h g-1(在100 秒内完全充满电),并且可以维持超过 10000 次循环,每次循环的容量衰减仅为 0.001%。原位同步辐射衍射表明,在电池循环过程中没有两相转变,而是单一的固溶行为。因此,钛酸锂水合物不仅可以作为需要煅烧的纳米结构中间产物,还可以作为理想的最终产物。水在高电压窗口的非质子电解液中通常是不利的。在这里,作者发现了一些钛酸锂水合物,它们在非质子电解液中具有优异的功率速率和超长的循环寿命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e18/5606990/9314dbc80613/41467_2017_574_Fig1_HTML.jpg

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