Details

Autor(en) / Beteiligte

• Wang, Junhao
• Jia, Hongfeng
• Liu, Zhaoli
• Yu, Jie
• Cheng, Linqi
• Wang, Heng‐Guo
• Cui, Fengchao
• Zhu, Guangshan

Titel

Anchoring π‐d Conjugated Metal–Organic Frameworks with Dual‐Active Centers on Carbon Nanotubes for Advanced Potassium‐Ion Batteries

Ist Teil von

• Advanced materials (Weinheim), 2024-02, Vol.36 (6), p.e2305605-n/a

Ort / Verlag

Germany: Wiley Subscription Services, Inc

Erscheinungsjahr

2024

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• Potassium‐ion batteries (PIBs) are gradually gaining attention owing to their natural abundance, excellent security, and high energy density. However, developing excellent organic cathode materials for PIBs to overcome the poor cycling stability and slow kinetics caused by the large radii of K+ ions is challenging. This study demonstrates for the first time the application of a hexaazanonaphthalene (HATN)‐based 2D π‐d conjugated metal–organic framework (2D c‐MOF) with dual‐active centers (Cu‐HATNH) and integrates Cu‐HATNH with carbon nanotubes (Cu‐HATNH@CNT) as the cathode material for PIBs. Owing to this systematic module integration and more exposed active sites with high utilization, Cu‐HATNH@CNT exhibits a high initial capacity (317.5 mA h g−1 at 0.1 A g−1), excellent long‐term cycling stability (capacity retention of 96.8% at 5 A g−1 after 2200 cycles), and outstanding rate capacity (147.1 mA h g−1 at 10 A g−1). The reaction mechanism and performance are determined by combining experimental characterization and density functional theory calculations. This contribution provides new opportunities for designing high‐performance 2D c‐MOF cathodes with multiple active sites for PIBs. This study demonstrates the first case of applying hexaazanonaphthalene (HATNH)‐based 2D conjugated metal–organic framework (Cu‐HATNH) integrated with carbon nanotubes via an in situ polymerization strategy to achieve stable long cycle stability and excellent rate performance with conjugated HATNH and unsaturated [CuO4] units as multiple redox active sites.