材料科学
杂原子
阳极
复合数
锂(药物)
兴奋剂
碳纤维
离子
纳米技术
化学工程
复合材料
电极
有机化学
光电子学
戒指(化学)
物理化学
医学
化学
工程类
内分泌学
作者
Jie Sun,Ping Li,Zhongling Cheng,Cheng Tang,Aijun Du,Haijiao Zhang
标识
DOI:10.1002/adfm.202500154
摘要
Abstract Bacteria‐derived carbon anode materials have shown appealing potential for advanced energy storage applications due to their low cost and good sustainability. However, the few intrinsic defects, sluggish transmission dynamics, and low capacity become the main bottleneck for their further development. Herein, the study designs a highly B, N co‐doped mesoporous carbon (BNMC)/staphylococcus aureus‐derived carbon (SAC) composite via a facile assembly route, followed by boron‐doping. Enabled by heteroatom doping and pore construction, the resulting BNMC/SAC anode for lithium‐ion batteries demonstrates a high reversible capacity of 621.77 mAh g −1 at 200 mA g −1 even after 500 cycles, and an excellent rate performance of 405.14 mAh g −1 at 2 A g −1 . Importantly, in situ/ex situ characterizations and theoretical simulation results further unveil that high B, N co‐doping along with a small amount of P doping can significantly increase the intrinsic defects of BNMC/SAC, thus providing more active sites for lithium‐ion storage. Furthermore, these structural features are conducive to improving the interfacial stability of the whole electrode, achieving a thin and uniform SEI film. The multi‐component co‐doping strategy along with pore engineering presents a scalable approach for enhancing the interfacial stability and transfer dynamics of carbon‐based electrode materials for low‐cost energy storage.
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