阳极
电化学
材料科学
成核
阴极
基质(水族馆)
化学工程
合金
金属
电极
钠
纳米技术
化学
冶金
工程类
地质学
有机化学
海洋学
物理化学
作者
Lulu Li,Ming Zhu,Guanyao Wang,Fangfang Yu,Liaoyong Wen,Huan Liu,Shi Xue Dou,Chao Wu
标识
DOI:10.1016/j.jechem.2022.04.019
摘要
Sodium (Na) metal anode exhibits a potential candidate in next-generation rechargeable batteries owing to its advantages of high earth abundance and low cost. Unfortunately, the practical development of sodium metal batteries is inherently plagued by challenges such as the side reactions and the growth of Na dendrites. Herein we report a highly stable Bi-based "sodiophilic" substrate to stabilize Na anode, which is created by in-situ electrochemical reactions of 3D hierarchical porous Bi2MoO6 (BMO) microspheres. BMO is initially transformed into the Bi "nanoseeds" embedded in the Na-Mo-O matrix. Subsequently, the Bi nanoseeds working as preferential nucleation sites through the formation of Bi-Na alloy enable the non-dendritic Na deposition. The asymmetric cells based on such BMO-based substrate can deliver a long-term cycling for 600 cycles at a large capacity of 4 mAh cm−2and for 800 cycles at a high current density of 10 mA cm−2. Even at a high depth of discharge (66.67%), the Na-predeposited BMO ([email protected]) electrodes can cycle for more than 1600 h. The limited [email protected] anodes coupled with the Na3V2(PO4)3 cathodes (N/P ratio of 3) in full cells also show excellent electrochemical performance with a capacity retention of about 97.4% after 1100 cycles at 2 C.
科研通智能强力驱动
Strongly Powered by AbleSci AI