超晶格
阴极
材料科学
离子
铝
插层(化学)
电池(电)
钨
扩散
化学工程
Crystal(编程语言)
纳米技术
光电子学
化学
无机化学
复合材料
冶金
物理化学
热力学
功率(物理)
有机化学
工程类
程序设计语言
物理
计算机科学
作者
Fangyan Cui,Mingshan Han,Wenyuan Zhou,Chen Lai,Yanhui Chen,Jingwen Su,Jinshu Wang,Hongyi Li,Yuxiang Hu
标识
DOI:10.1002/smtd.202201281
摘要
Rechargeable aluminum batteries (RABs), with abundant aluminum reserves, low cost, and high safety, give them outstanding advantages in the postlithium batteries era. However, the high charge density (364 C mm-3 ) and large binding energy of three-electron-charge aluminum ions (Al3+ ) de-intercalation usually lead to irreversible structural deterioration and decayed battery performance. Herein, to mitigate these inherent defects from Al3+ , an unexplored family of superlattice-type tungsten selenide-sodium dodecylbenzene sulfonate (SDBS) (S-WSe2 ) cathode in RABs with a stably crystal structure, expanded interlayer, and enhanced Al-ion diffusion kinetic process is proposed. Benefiting from the unique advantage of superlattice-type structure, the anionic surfactant SDBS in S-WSe2 can effectively tune the interlayer spacing of WSe2 with released crystal strain from high-charge-density Al3+ and achieve impressively long-term cycle stability (110 mAh g-1 over 1500 cycles at 2.0 A g-1 ). Meanwhile, the optimized S-WSe2 cathode with intrinsic negative attraction of SDBS significantly accelerates the Al3+ diffusion process with one of the best rate performances (165 mAh g-1 at 2.0 A g-1 ) in RABs. The findings of this study pave a new direction toward durable and high-performance electrode materials for RABs.
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