Triple Templates Directed Synthesis of Nitrogen-Doped Hierarchically Porous Carbons from Pyridine Rich Monomer as Efficient and Reversible SO 2 Adsorbents
Herein, a variety of 2,6-diaminopyridine (DAP) derived nitrogen-doped hierarchically porous carbon (DAP-NHPC-T) prepared from carbonization-induced structure transformation of DAP-Zn-SiO -P123 nanocomposites are reported, which are facilely prepared from solvent-free co-assembly of block copolymer t...
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Published in | Small (Weinheim an der Bergstrasse, Germany) p. e2404548 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
02.08.2024
|
Subjects | |
Online Access | Get full text |
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Summary: | Herein, a variety of 2,6-diaminopyridine (DAP) derived nitrogen-doped hierarchically porous carbon (DAP-NHPC-T) prepared from carbonization-induced structure transformation of DAP-Zn-SiO
-P123 nanocomposites are reported, which are facilely prepared from solvent-free co-assembly of block copolymer templates P123 with pyridine-rich monomer of DAP, Zn(NO
)
and tetramethoxysilane. In the pyrolysis process, P123 and SiO
templates promote the formation of mesoporous and supermicroporous structures in the DAP-NHPC-T, while high-temperature volatilization of Zn contributed to generation of micropores. The DAP-NHPC-T possess large BET surface areas (≈956-1126 m
g
), hierarchical porosity with micro-supermicro-mesoporous feature and high nitrogen contents (≈10.44-5.99 at%) with tunable density of pyridine-based nitrogen sites (≈5.99-3.32 at%), exhibiting good accessibility and reinforced interaction with SO
. Consequently, the DAP-NHPC-T show high SO
capacity (14.7 mmol g
, 25 °C and 1.0 bar) and SO
/CO
/N
IAST selectivities, extraordinary dynamic breakthrough separation efficiency and cycling stability, far beyond any other reported nitrogen-doped metal-free carbon. As verified by in situ spectroscopy and theoretical calculations, the pyridine-based nitrogen sites of the DAP-NHPC-T boost SO
adsorption via the unique charge transfer, the adsorption mechanism and reaction model have been finally clarified. |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.202404548 |