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In Situ Doping Strategy for the Preparation of Conjugated Triazine Frameworks Displaying Efficient CO2 Capture Performance
被引:211
|作者:
Zhu, Xiang
[1
]
Tian, Chengcheng
[1
]
Veith, Gabriel M.
[3
]
Abney, Carter W.
[2
]
Dehaudt, Jeremy
[1
]
Dai, Sheng
[1
,2
]
机构:
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
[3] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
关键词:
CARBON-DIOXIDE CAPTURE;
POROUS POLYMER NETWORKS;
COVALENT ORGANIC FRAMEWORKS;
SELECTIVE ADSORPTION;
SURFACE-AREA;
GAS-STORAGE;
SEPARATION;
FUNCTIONALIZATION;
TEMPERATURE;
INSERTION;
D O I:
10.1021/jacs.6b07644
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
An in situ doping strategy has been developed for the generation of a novel family of hexaazatriphenylene-based conjugated triazine frameworks (CTFs) for efficient CO2 capture. The resulting task specific materials exhibit an exceptionally high CO2 uptake capacity (up to 4.8 mmol g(-1) at 297 K and 1 bar). The synergistic effects of ultrananoporosity and rich N/O codoped CO2-philic sites bestow the framework with the highest CO2 adsorption capacity among known porous organic polymers (POPs). This innovative approach not only enables superior CO2 separation performance but also provides tunable control of surface features on POPs, thereby affording control over bulk material properties. We anticipate this novel strategy will facilitate new possibilities for the rational design and synthesis of nanoporous materials for carbon capture.
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页码:11497 / 11500
页数:4
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