材料科学
纳米孔
硫化物
异质结
离子
碳纤维
化学工程
纳米技术
复合材料
光电子学
冶金
复合数
有机化学
工程类
化学
作者
Naixuan Ci,Xianke Yue,Jun Miao,Boxuan Cao,Jingchen He,X.A. Wang,Xun Yi,Yinghe Zhang,Kolan Madhav Reddy,Hua‐Jun Qiu
标识
DOI:10.1002/adfm.202514133
摘要
Abstract Transition metal sulfides are promising sodium‐ion battery anodes. Herein, a multicomponent MnNiFe‐based sulfide heterojunction with ultrafine nanoporous structure and inherent 3D carbon coating is synthesized using commercially available MnNiFeCO 3 as the precursor. It is found that the multicomponent metal interaction greatly inhibits the surface diffusion during carbonate decomposition process, resulting in ultrafine nanoporous MnNi(Fe)O 3 (≤ 10 nm) with a much larger surface area when compared with a single metal‐based counterpart. To enhance the conductivity and structure stability of the heterojunction, a thin layer of N, S‐doped 3D porous carbon is inherently coated on the nanoporous MnNiFeS x (NS‐C@MnNiFeS) by first forming a 3D polyaniline layer on the nanoporous MnNi(Fe)O 3 , which is then transformed into doped carbon during the vulcanization process. Owing to the multicomponent heterojunction design (which may provide more active sites for effective Na + adsorption), much increased specific surface area, and 3D inherent carbon coating, the NS‐C@MnNiFeS exhibits significantly enhanced performance for Na + storage. After 90 cycles at 0.1 A g −1 , a record‐high reversible capacity of 859.2 mAh g −1 is achieved, and it can be stably cycled for 1500 cycles at a current density of 10.0 A g −1 . DFT calculation reveals the modified electronic structure and enhanced Na + adsorption by constructing the heterojunction.
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