黑磷
钾
接口(物质)
部分
磷
动力学
离子
化学工程
聚合
材料科学
超分子化学
相(物质)
两亲性
炭黑
碳纤维
图层(电子)
之字形的
纳米技术
化学
基质(化学分析)
催化作用
分子
工作(物理)
理论(学习稳定性)
作者
Guohui Qin,Hao Xu,Mingbo Wu,Feixiang Wu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-18
卷期号:64 (51): e202514456-e202514456
被引量:2
标识
DOI:10.1002/anie.202514456
摘要
Black phosphorus (BP), exhibiting a large spatial layer and high theoretical capacity, has been heralded as a promising candidate for K+ storage. Nevertheless, the unpredictability of the structural/interfacial reconstruction guides the arduous kinetics and poor stability, especially conferring to high current density and wide-temperature operation. To address these challenges, self-adaptive interface reconstruction with a multiple secondary bonds mediation (IRSM) strategy is adopted for amphipathic BP complex to improve kinetics and stability, wherein BP nanospheres encapsulated into a sacciform B-doped carbon matrix (BC) are further grafted with polybromoisobutyryloxy benzenesulfonic (PBBS), which undergoes in situ polymerization and is transformed into metal-organic bromoisobutyrylox supramolecular (PBS). Consequently, combining the flexibility/rigidity advantage of organic moiety and the stability advantage of inorganic moiety, BC@BP@PBS manifests excellent fast charging behaviors, a wide-temperature operation from -70 °C to 80 °C, and an extended cycle life of up to 1300 cycles. This work builds an ingenious protocol for leveraging the trade-off between fast charging, wide-temperature operation, and long life span for high-performance cell devices.
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