Dai Liyufen, Zhong Xiangli, Zou Juan, Fu Bi, Su Yong, Ren Chuanlai, Wang Jinbin, Zhong Gaokuo
Shenzhen Key Laboratory of Nanobiomechanics, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
School of Materials Science and Engineering, Xiangtan University, Xiangtan 411105, China.
Nanomaterials (Basel). 2021 May 15;11(5):1307. doi: 10.3390/nano11051307.
SnO, a typical transition metal oxide, is a promising conversion-type electrode material with an ultrahigh theoretical specific capacity of 1494 mAh g. Nevertheless, the electrochemical performance of SnO electrode is limited by large volumetric changes (~300%) during the charge/discharge process, leading to rapid capacity decay, poor cyclic performance, and inferior rate capability. In order to overcome these bottlenecks, we develop highly ordered SnO nanopillar array as binder-free anodes for LIBs, which are realized by anodic aluminum oxide-assisted pulsed laser deposition. The as-synthesized SnO nanopillar exhibit an ultrahigh initial specific capacity of 1082 mAh g and maintain a high specific capacity of 524/313 mAh g after 1100/6500 cycles, outperforming SnO thin film-based anodes and other reported binder-free SnO anodes. Moreover, SnO nanopillar demonstrate excellent rate performance under high current density of 64 C (1 C = 782 mA g), delivering a specific capacity of 278 mAh g, which can be restored to 670 mAh g after high-rate cycling. The superior electrochemical performance of SnO nanoarray can be attributed to the unique architecture of SnO, where highly ordered SnO nanopillar array provided adequate room for volumetric expansion and ensured structural integrity during the lithiation/delithiation process. The current study presents an effective approach to mitigate the inferior cyclic performance of SnO-based electrodes, offering a realistic prospect for its applications as next-generation energy storage devices.
SnO是一种典型的过渡金属氧化物,是一种很有前景的转换型电极材料,其理论比容量高达1494 mAh g。然而,SnO电极的电化学性能受到充放电过程中较大体积变化(约300%)的限制,导致容量快速衰减、循环性能差和倍率性能不佳。为了克服这些瓶颈,我们开发了高度有序的SnO纳米柱阵列作为锂离子电池的无粘结剂阳极,这是通过阳极氧化铝辅助脉冲激光沉积实现的。合成的SnO纳米柱具有1082 mAh g的超高初始比容量,在1100/6500次循环后保持524/313 mAh g的高比容量,优于基于SnO薄膜的阳极和其他报道的无粘结剂SnO阳极。此外,SnO纳米柱在64 C(1 C = 782 mA g)的高电流密度下表现出优异的倍率性能,比容量为278 mAh g,在高速率循环后可恢复到670 mAh g。SnO纳米阵列优异的电化学性能可归因于SnO独特的结构,其中高度有序的SnO纳米柱阵列为体积膨胀提供了足够的空间,并确保了锂化/脱锂过程中的结构完整性。当前的研究提出了一种有效方法来缓解基于SnO的电极较差的循环性能,为其作为下一代储能装置的应用提供了现实前景。