Kinetically Controlled Assembly of Nitrogen-Doped Invaginated Carbon Nanospheres with Tunable Mesopores

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• 作者：Yang Liu ; Dr. Hongwei Zhang ; Owen Noonan ; Chun Xu ; Dr. Yuting Niu ; Yannan Yang ; Prof. Liang Zhou ; Dr. Xiaodan Huang and Prof. Chengzhong Yu
• 刊名：Chemistry - A European Journal
• 出版年：2016
• 出版时间：October 10, 2016
• 年：2016
• 卷：22
• 期：42
• 页码：14962-14967
• 全文大小：1620K
• ISSN：1521-3765

文摘

Mesoporous hollow carbon nanospheres (MHCS) have been extensively studied owning to their unique structural features and diverse potential applications. A surfactant-free self-assembly approach between resorcinol/formaldehyde and silicon alkoxide has emerged as an important strategy to prepare MHCS. Extending such a strategy to other substituted phenols to produce heterogeneous-atom-doped MHCS remains a challenge due to the very different polymerization kinetics of various resins. Herein, we report an ethylenediamine-assisted strategy to control the cooperative self-assembly between a 3-aminophenol/formaldehyde resin and silica templates. Nitrogen-doped mesoporous invaginated carbon nanospheres (N-MICS) with an N content of 6.18 at %, high specific surface areas (up to 1118 m² g⁻¹), large pore volumes (2.47 cm³ g⁻¹), and tunable mesopores (3.7–11.1 nm) have been prepared. When used as electrical double-layer supercapacitors, N-MICS show a high capacitance of 261 F g⁻¹, an outstanding cycling stability (≈94 % capacitance retention after 10 000 cycles), and a good rate performance.