Superlattice-Stabilized WSe2 Cathode for Rechargeable Aluminum Batteries

被引:27
作者
Cui, Fangyan [1 ]
Han, Mingshan [1 ]
Zhou, Wenyuan [1 ]
Lai, Chen [1 ]
Chen, Yanhui [1 ]
Su, Jingwen [1 ]
Wang, Jinshu [1 ]
Li, Hongyi [1 ]
Hu, Yuxiang [1 ]
机构
[1] Beijing Univ Technol, Fac Mat & Mfg, Key Lab Adv Funct Mat, Beijing 100124, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
electrode pulverization; long-term stability; rechargeable aluminum batteries; superlattice-type cathodes; tungsten selenide; ENERGY-STORAGE; CRYSTALS;
D O I
10.1002/smtd.202201281
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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+) deintercalation 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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页数:9
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