Zhang Ying, Luo Wei, Wang Chengwei, Li Yiju, Chen Chaoji, Song Jianwei, Dai Jiaqi, Hitz Emily M, Xu Shaomao, Yang Chunpeng, Wang Yanbin, Hu Liangbing
Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742.
Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742
Proc Natl Acad Sci U S A. 2017 Apr 4;114(14):3584-3589. doi: 10.1073/pnas.1618871114. Epub 2017 Mar 20.
Lithium metal anode with the highest capacity and lowest anode potential is extremely attractive to battery technologies, but infinite volume change during the Li stripping/plating process results in cracks and fractures of the solid electrolyte interphase, low Coulombic efficiency, and dendritic growth of Li. Here, we use a carbonized wood (C-wood) as a 3D, highly porous (73% porosity) conductive framework with well-aligned channels as Li host material. We discovered that molten Li metal can infuse into the straight channels of C-wood to form a Li/C-wood electrode after surface treatment. The C-wood channels function as excellent guides in which the Li stripping/plating process can take place and effectively confine the volume change that occurs. Moreover, the local current density can be minimized due to the 3D C-wood framework. Therefore, in symmetric cells, the as-prepared Li/C-wood electrode presents a lower overpotential (90 mV at 3 mA⋅cm), more-stable stripping/plating profiles, and better cycling performance (∼150 h at 3 mA⋅cm) compared with bare Li metal electrode. Our findings may open up a solution for fabricating stable Li metal anode, which further facilitates future application of high-energy-density Li metal batteries.
具有最高容量和最低阳极电位的锂金属阳极对电池技术极具吸引力,但锂剥离/电镀过程中的无限体积变化会导致固体电解质界面的裂纹和断裂、低库仑效率以及锂的枝晶生长。在此,我们使用碳化木材(C-wood)作为具有排列良好通道的三维、高孔隙率(73%孔隙率)导电框架作为锂宿主材料。我们发现,经过表面处理后,熔融锂金属可以注入C-wood的直通道中形成Li/C-wood电极。C-wood通道起到了出色的导向作用,锂剥离/电镀过程可以在其中发生,并有效限制体积变化。此外,由于三维C-wood框架,局部电流密度可以最小化。因此,在对称电池中,与裸锂金属电极相比,所制备的Li/C-wood电极具有更低的过电位(3 mA·cm²时为90 mV)、更稳定的剥离/电镀曲线以及更好的循环性能(3 mA·cm²时约150小时)。我们的发现可能为制造稳定的锂金属阳极开辟一种解决方案,这进一步促进了高能量密度锂金属电池的未来应用。