Abstract

Developing porous carbon with suitable microporous structure and large effective surface area is crucial for pursuing high volumetric performance of organic supercapacitors. Herein, we proposed a homogeneous activation method to regulate the interconnected microporous structure of porous carbon through choosing the alkali metal ion activators (Li+, K+, Cs+). We have revealed the pore evolution mechanism from the points of ion activation strength, cluster transport, and metal boiling points. Compared to others, the optimized sample activated by Cs+ shows large micropore volume, high effective surface area (2463 m2 g−1), and high compaction density (0.75 g cm−3), performing an improved volumetric capacitance (126 F cm−3 at 1 A g−1) and good rate performance (79 F cm−3 at 20 A g−1) in organic electrolyte. The symmetric supercapacitor at the commercial electrode mass loading shows a competitive energy density (23.9 Wh L−1 at 211.4 W L−1, 4 Wh L−1 at 1638 W L−1). Moreover, this pore-regulating strategy has a general availability when using other non-foaming carbon precursors, which will open up new paths for improving the surface and space utilization of porous carbon for compact capacitive energy storage.

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