材料科学
单晶
Crystal(编程语言)
离子
钠
光电子学
化学工程
纳米技术
结晶学
化学
冶金
计算机科学
工程类
有机化学
程序设计语言
作者
Le Zhang,Jieyou Huang,Miaoyan Song,Lu Chen,Wenwei Wu,Xuehang Wu
标识
DOI:10.1021/acsami.3c10312
摘要
An increase in the size of single-crystal particles can effectively reduce the interfacial side reactions of layered oxides for sodium-ion batteries at high voltages but may result in sluggish Na + transport. Herein, single-crystal Na 0.66 Ni 0.26 Zn 0.07 Mn 0.67 O 2 with increased proportions of {010} planes is synthesized by adding low-cost NaCl as the molten salt. With the assistance of a NaCl molten salt, the median diameter (D50) of single-crystal Na 0.66 Ni 0.26 Zn 0.07 Mn 0.67 O 2 increases to 10.46 μm relative to that of the comparison sample without NaCl (6.57 μm). Electrolyte decomposition on the surface of single-crystal Na 0.66 Ni 0.26 Zn 0.07 Mn 0.67 O 2 is considerably suppressed, owing to a decrease in the specific surface area. Moreover, the increased exposure of {010} planes is favorable for improving the Na + transport kinetics of single-crystal particles. Therefore, at 100 mA g –1, single-crystal Na 0.66 Ni 0.26 Zn 0.07 Mn 0.67 O 2 exhibits a high-capacity retention of 96.6% after 100 cycles, which is considerably greater than that of the comparison sample (86.8%). Moreover, the rate performance of single-crystal Na 0.66 Ni 0.26 Zn 0.07 Mn 0.67 O 2 (average discharge capacity of 81.2 mAh g –1 ) is superior to that of the comparison sample (average discharge capacity of 61.2 mAh g –1 ) at 2000 mA g –1 . This work provides a new approach for promoting the single-crystal growth of layered oxides for highly stable interfaces at high voltages without compromising Na + transport kinetics.
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