Clark Cassius, O'Keefe Christopher A, Wright Dominic S, Grey Clare P
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB21EW, UK.
Cambridge Graphene Centre, University of Cambridge, 9 JJ Thompson Avenue, Cambridge, CB30FA, UK.
ChemSusChem. 2025 Jun 17;18(12):e202500103. doi: 10.1002/cssc.202500103. Epub 2025 Apr 23.
Phosphorus-doped carbons provide a balance between the electrochemical stability of graphitic lattices and the high energy density of phosphorus materials when used in lithium and sodium-ion batteries. Herein, a comprehensive ex situ P, Li, and Na solid-state nuclear magnetic resonance analysis of the intercalation mechanism of novel, stable, dual-phase phosphorus-doped, and phosphorus-encapsulated turbostratic graphite microspheres is presented. Results indicate that lithium intercalation occurs through the formation of LiP from white phosphorus trapped within the graphitic layers, with the involvement of lithiated phosphorus atoms within the graphitic lattice. A dual-lithiated carbon doped-phosphorus environment is tentatively proposed at low voltages. Sodiation occurs through a similar mechanism; however, no evidence of a dual-sodiated doped-phosphorus environment is observed. Upon removal of ions, carbon-encapsulated phosphorus with a local structure similar to red phosphorus forms, which subsequently allows effective reversible ion storage.
磷掺杂碳在用于锂和钠离子电池时,能在石墨晶格的电化学稳定性与磷材料的高能量密度之间实现平衡。本文对新型、稳定、双相磷掺杂和磷包覆的乱层石墨微球的嵌入机制进行了全面的非原位磷、锂和钠固态核磁共振分析。结果表明,锂嵌入是通过石墨层中捕获的白磷形成LiP来实现的,石墨晶格中锂化的磷原子也参与其中。在低电压下初步提出了双锂化碳掺杂磷环境。钠化通过类似的机制发生;然而,未观察到双钠化掺杂磷环境的证据。去除离子后,形成了具有类似于红磷局部结构的碳包覆磷,随后实现了有效的可逆离子存储。