阳极
材料科学
离子
电化学
硒化物
锰
钠
电极
电解质
阴极
化学
物理化学
有机化学
冶金
硒
作者
Shaokun Chong,Ting Li,Shuangyan Qiao,Yi‐Chun Yang,Zhengqing Liu,Jing Yang,Hsing‐Yu Tuan,Guozhong Cao,Wei Huang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-01-18
卷期号:18 (4): 3801-3813
被引量:6
标识
DOI:10.1021/acsnano.3c12215
摘要
Sodium-ion batteries (SIBs) have been extensively studied owing to the abundance and low-price of Na resources. However, the infeasibility of graphite and silicon electrodes in sodium-ion storage makes it urgent to develop high-performance anode materials. Herein, α-MnSe nanorods derived from δ-MnO2 (δ−α-MnSe) are constructed as anodes for SIBs. It is verified that α-MnSe will be transferred into β-MnSe after the initial Na-ion insertion/extraction, and δ−α-MnSe undergoes typical conversion mechanism using a Mn-ion for charge compensation in the subsequent charge–discharge process. First-principles calculations support that Na-ion migration in defect-free α-MnSe can drive the lattice distortion to phase transition (alpha → beta) in thermodynamics and dynamics. The formed β-MnSe with robust lattice structure and small Na-ion diffusion barrier boosts great structure stability and electrochemical kinetics. Hence, the δ−α-MnSe electrode contributes excellent rate capability and superior cyclic stability with long lifespan over 1000 cycles and low decay rate of 0.0267% per cycle. Na-ion full batteries with a high energy density of 281.2 Wh·kg–1 and outstanding cyclability demonstrate the applicability of δ−α-MnSe anode.
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