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  4. Multilayer-graphene-stabilized lithium deposition for anode-Free lithium-metal batteries
 
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Multilayer-graphene-stabilized lithium deposition for anode-Free lithium-metal batteries

Journal
Nanoscale
Journal Volume
11
Journal Issue
6
Pages
2710-2720
Date Issued
2019
Author(s)
Assegie A.A.
Chung C.-C.
Tsai M.-C.
Su W.-N.
CHUN-WEI CHEN  
Hwang B.-J.
DOI
10.1039/c8nr06980h
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85061135730&doi=10.1039%2fc8nr06980h&partnerID=40&md5=7388de3f2e3b5397987b8c421bbf2356
https://scholars.lib.ntu.edu.tw/handle/123456789/432774
Abstract
The will to circumvent capacity fading, Li dendrite formation, and low coulombic efficiency in anode-free Li-metal batteries (AFLMBs) requires a radical change in the science underpinning new materials discovery, battery design, and understanding electrode interfaces. Herein, a Cu current collector formed with ultrathin multilayer graphene grown via chemical vapor deposition (CVD) was used as an artificial layer to stabilize the electrode interface and sandwich-deposited Li with Cu. A multilayer graphene film's superior strength, chemical stability, and flexibility make it an excellent choice to modify a Cu electrode. Fabricating an anode bigger than the cathode improved the alignment of the electrodes during assembly, minimizing interfacial stress. Here, 19 mm electrodes when paired with a commercial LiFePO4 cathode (mass loading: ∼12 mg cm-2) delivered the first-cycle discharge capacities of 147 and 151 mA h g-1 for bare and multilayer-graphene-protected electrodes, respectively, which could alleviate the big hurdle (initial capacity loss) in anode-free batteries. After 100 round-trip cycles, bare Cu and multilayer-graphene-protected electrodes retained ∼46 and ∼61% of their initial capacities, respectively, in an ether-based electrolyte at the rate of 0.1 C.
SDGs

[SDGs]SDG7

Publisher
Royal Society of Chemistry
Type
journal article

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