分离器(采油)
金属锂
阴极
材料科学
固态
锂(药物)
磷酸钒锂电池
金属
电池(电)
锂电池
聚合物
化学工程
无机化学
复合材料
化学
阳极
电极
冶金
热力学
有机化学
物理化学
离子
物理
工程类
功率(物理)
离子键合
内分泌学
医学
作者
Gerrit Homann,Qing Wang,Sufu Liu,Antoine Devincenti,Pranav Karanth,Mark Weijers,Fokko M. Mulder,Matiss Piesins,Tom Gouveia,Alix Ladam,Sébastien Fantini,Corsin Battaglia
标识
DOI:10.1021/acsaem.4c02099
摘要
High Resolution Image Download MS PowerPoint Slide Solid-state batteries with lithium metal anodes are considered the next major technology leap with respect to today’s lithium-ion batteries, as they promise a significant increase in energy density. Expectations for solid-state batteries from the automotive and aviation sectors are high, but their implementation in industrial production remains challenging. Here, we report a solid-state lithium–metal battery enabled by a polymer electrolyte consisting of a poly(DMADAFSI) cationic polymer and LiFSI in Pyr 13 FSI as plasticizer. The polymer electrolyte is infiltrated and solidified in the pores of a commercial LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NMC811) cathode with up to 2.8 mAh cm –2 nominal areal capacity and in the pores of a 25 μm thin commercial polypropylene separator. Cathode and separator are finally laminated into a cell in combination with a commercial 20 μm thin lithium metal anode. Our demonstration of a solid-state polymer battery cycling at full nominal capacity employing exclusively commercially available components available at industrial scale represents a critical step forward toward the commercialization of a competitive all-solid-state battery technology.
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