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A Molecular Foaming and Activation Strategy to Porous N-Doped Carbon Foams for Supercapacitors and CO₂ Capture.

ABSTRACT: Hierarchically porous carbon materials are promising for energy storage, separation and catalysis. It is desirable but fairly challenging to simultaneously create ultrahigh surface areas, large pore volumes and high N contents in these materials. Herein, we demonstrate a facile acid-base enabled in situ molecular foaming and activation strategy for the synthesis of hierarchically macro-/meso-/microporous N-doped carbon foams (HPNCFs). The key design for the synthesis is the selection of histidine (His) and potassium bicarbonate (PBC) to allow the formation of 3D foam structures by in situ foaming, the PBC/His acid-base reaction to enable a molecular mixing and subsequent a uniform chemical activation, and the stable imidazole moiety in His to sustain high N contents after carbonization. The formation mechanism of the HPNCFs is studied in detail. The prepared HPNCFs possess 3D macroporous frameworks with thin well-graphitized carbon walls, ultrahigh surface areas (up to 3200 m² g^-1), large pore volumes (up to 2.0 cm³ g^-1), high micropore volumes (up to 0.67 cm³ g^-1), narrowly distributed micropores and mesopores and high N contents (up to 14.6 wt%) with pyrrolic N as the predominant N site. The HPNCFs are promising for supercapacitors with high specific capacitances (185-240 F g^-1), good rate capability and excellent stability. They are also excellent for CO₂ capture with a high adsorption capacity (~ 4.13 mmol g^-1), a large isosteric heat of adsorption (26.5 kJ mol^-1) and an excellent CO₂/N₂ selectivity (~ 24).

SUBMITTER: Zhou M

PROVIDER: S-EPMC7770655 | biostudies-literature |

REPOSITORIES: biostudies-literature

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