Nanomaterials and Environmental Detection Laboratory, Institute of Intelligent Machines, Chinese Academy of Sciences , Hefei, Anhui 230031, China.
Department of Materials Science and Engineering, Department of Chemistry, Frederick Seitz Materials Research Laboratory, and Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign , Urbana, Illinois 61801, United States.
Nano Lett. 2016 Jul 13;16(7):4501-7. doi: 10.1021/acs.nanolett.6b01711. Epub 2016 Jun 28.
High volumetric energy density secondary batteries are important for many applications, which has led to considerable efforts to replace the low volumetric capacity graphite-based anode common to most Li-ion batteries with a higher energy density anode. Because most high capacity anode materials expand significantly during charging, such anodes must contain sufficient porosity in the discharged state to enable the expansion, yet not excess porosity, which lowers the overall energy density. Here, we present a high volumetric capacity anode consisting of a three-dimensional (3D) nanocomposite formed in only a few steps which includes both a 3D structured Sn scaffold and a hollow Sn sphere within each cavity where all the free Sn surfaces are coated with carbon. The anode exhibits a high volumetric capacity of ∼1700 mA h cm(-3) over 200 cycles at 0.5C, and a capacity greater than 1200 mA h cm(-3) at 10C. Importantly, the anode can even be formed into a commercially relevant ∼100 μm thick form. When assembled into a full cell the anode shows a good compatibility with a commercial LiMn2O4 cathode. In situ TEM observations confirm the electrode design accommodates the necessary volume expansion during lithiation.
高体积能量密度二次电池对于许多应用非常重要,这导致人们付出了相当大的努力,用更高能量密度的阳极取代大多数锂离子电池中常见的低体积容量石墨基阳极。由于大多数高容量阳极材料在充电时会显著膨胀,因此这种阳极在放电状态下必须具有足够的孔隙率以允许膨胀,但又不能有过多的孔隙率,否则会降低整体能量密度。在这里,我们提出了一种由仅通过少数几个步骤形成的三维(3D)纳米复合材料组成的高体积容量阳极,其中包括 3D 结构的 Sn 支架和每个腔室内的空心 Sn 球,其中所有游离 Sn 表面都涂有碳。该阳极在 0.5C 下经过 200 次循环后,具有约 1700 mA h cm(-3)的高体积容量,在 10C 时的容量大于 1200 mA h cm(-3)。重要的是,该阳极甚至可以形成具有商业相关的约 100 μm 厚的形式。将其组装成全电池时,该阳极与商业 LiMn2O4 阴极具有良好的兼容性。原位 TEM 观察证实了电极设计适应了在锂化过程中必要的体积膨胀。