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An α-MnSe nanorod as anode for superior potassium-ion storage via synergistic effects of physical encapsulation and chemical bonding

阳极 石墨烯 电化学 纳米棒 材料科学 X射线光电子能谱 化学工程 电极 纳米技术 化学 工程类 物理化学
作者
Ting Li,Yikun Wang,Lingling Yuan,Qianwen Zhou,Shuangyan Qiao,Zhengqing Liu,Shaokun Chong
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:446: 137152-137152 被引量:33
标识
DOI:10.1016/j.cej.2022.137152
摘要

• α-MnSe nanorods wrapped by N-doped carbon and graphene are constructed as anodes for PIBs. • α-MnSe@NC@graphene exhibits excellent electrochemical properties. • The K-ion storage mechanism is revealed by ex situ TEM and XPS analyses. • Synergistic effects of physical encapsulation and chemical bonding boost electrode stability. Conversion mechanism anode materials have been widely employed for potassium ion batteries (PIBs) due to high theoretical specific capacities. However, large volume expansion and poor electrochemical kinetics have become the key bottlenecks hindering its further development. Herein, α-MnSe nanorods wrapped by N-doped carbon and graphene (α-MnSe@NC@graphene) are constructed as anode materials for PIBs. The architecture can not only provide superior electrode integrity to buffer volume variation and maintain structure stability via synergistic effects of physical encapsulation and Mn-C chemical bonding, but also serve as conductive network to accelerate the electron transfer and K-ion diffusion. As a result, α-MnSe@NC@graphene composite delivers high initial charge specific capacity of 307.9 mAh·g −1 and great cycling stability over 250 cycles with the capacity retention of 232.8 mAh·g −1 at 50 mA·g −1 . Besides, superior rate capability (91.1 mAh·g −1 at 2.0 A·g −1 ) and long lifespan over 700 cycles at 1.0 A·g −1 with the low capacities decay rate of 0.064% per cycle can be acquired. Ex situ TEM and XPS results verify that K-ion insert into/extract from α-MnSe@NC@graphene through a conversion mechanism based on the Mn-ion redox site (MnSe + 2 K + + 2e - ↔ Mn + K 2 Se).
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