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Heteroatom-Containing Porous Carbons Derived from Ionic Liquid-Doped Alkali Organic Salts for Supercapacitors

机译:离子液体掺杂的碱金属超级电容器衍生的含杂原子的多孔碳

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A simple strategy for the synthesis of heteroatom-doped porous carbon materials (CMs) via using ionic liquid (IL)-doped alkali organic salts as small molecular precursors is developed. Doping of alkali organic salts (such as sodium glutamate, sodium tartrate, and sodium citrate) with heteroatoms containing ILs (including 1-butyl-3-methylimidazolium chlorine and 3-butyl-4-methythiazolebromination) not only incorporates the heteroatoms into the carbon frameworks but also highly improves the carbonization yield, as compared with that of either alkali organic salts or ILs as precursors. The porous structure of CMs can be tuned by adjusting the feed ratio of ILs. The porous CMs derived from 1-butyl-3-methylimidazolium chlorine-doped sodium glutamate exhibit high charge storage capacity with a specific capacitance of 287 F g(-1) and good stability over 5000 cycles in 6 m KOH at a current density of 1 A g(-1) for supercapacitors. This strategy opens a simple and efficient method for the synthesis of heteroatom-doped porous CMs.
机译:开发了一种简单的策略,通过使用离子液体(IL)掺杂的碱金属有机盐作为小分子前体来合成杂原子掺杂的多孔碳材料(CMs)。用含IL的杂原子(包括1-丁基-3-甲基咪唑鎓氯和3-丁基-4-甲基噻唑溴化)掺杂碱性有机盐(如谷氨酸钠,酒石酸钠和柠檬酸钠)不仅将杂原子掺入碳骨架中与碱金属有机盐或ILs的前驱体相比,它还能大大提高碳化率。 CM的多孔结构可以通过调节IL的进料比来调节。源自1-丁基-3-甲基咪唑鎓氯掺杂的谷氨酸钠的多孔CM表现出高电荷存储容量,比电容为287 F g(-1),并且在电流密度为1的情况下在6 m KOH中经过5000次循环具有良好的稳定性。超级电容器的g(-1)。该策略为合成杂原子掺杂的多孔CM开辟了一种简单有效的方法。

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