Cooperative Carbon Dioxide Capture in Diamine-Appended Magnesium-Olsalazine Frameworks

被引:18
|
作者
Zhu, Ziting [1 ,2 ,3 ]
Parker, Surya T. [3 ,4 ]
Forse, Alexander C. [2 ,4 ,5 ]
Lee, Jung-Hoon [6 ,7 ,8 ]
Siegelman, Rebecca L. [2 ,3 ,9 ]
Milner, Phillip J. [2 ,3 ,10 ]
Tsai, Hsinhan [2 ,3 ]
Ye, Mengshan [2 ]
Xiong, Shuoyan [2 ]
Paley, Maria V. [2 ]
Uliana, Adam A. [3 ,4 ]
Oktawiec, Julia [2 ]
Dinakar, Bhavish [3 ,4 ]
Didas, Stephanie A. [3 ]
Meihaus, Katie R. [2 ]
Reimer, Jeffrey A. [4 ]
Neaton, Jeffrey B. [6 ,7 ]
Long, Jeffrey R. R. [2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[5] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[6] Univ Calif Berkeley, Dept Phys, Berkeley, CA 94720 USA
[7] Lawrence Berkeley Natl Lab, Mol Foundry, Berkeley, CA 94720 USA
[8] Korea Inst Sci & Technol KIST, Computat Sci Res Ctr, Seoul 02792, South Korea
[9] DuPont de Nemours Inc, 200 Powder Mill Rd, Wilmington, DE 19803 USA
[10] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
METAL-ORGANIC FRAMEWORK; POSTCOMBUSTION CO2 CAPTURE; FLUE-GAS; SOLID SORBENTS; ADSORPTION; AMINE; DEGRADATION; ADSORBENTS; AMMONIUM; AIR;
D O I
10.1021/jacs.3c03870
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Diamine-appended Mg-2(dobpdc) (dobpdc(4-) = 4,4 & PRIME;-dioxidobiphenyl-3,3 & PRIME;-dicarboxylate) metal-organicframeworks have emerged as promising candidates for carbon captureowing to their exceptional CO2 selectivities, high separationcapacities, and step-shaped adsorption profiles, which arise froma unique cooperative adsorption mechanism resulting in the formationof ammonium carbamate chains. Materials appended with primary,secondary-diamines featuring bulky substituents,in particular, exhibit excellent stabilities and CO2 adsorptionproperties. However, these frameworks display double-step adsorptionbehavior arising from steric repulsion between ammonium carbamates,which ultimately results in increased regeneration energies. Herein,we report frameworks of the type diamine-Mg-2(olz)(olz(4-) = (E)-5,5 & PRIME;-(diazene-1,2-diyl)bis(2-oxidobenzoate))that feature diverse diamines with bulky substituents and displaydesirable single-step CO2 adsorption across a wide rangeof pressures and temperatures. Analysis of CO2 adsorptiondata reveals that the basicity of the pore-dwelling amine inaddition to its steric bulk is an important factor influencingadsorption step pressure; furthermore, the amine steric bulk is foundto be inversely correlated with the degree of cooperativity in CO2 uptake. One material, ee-2-Mg-2(olz) (ee-2= N,N-diethylethylenediamine), adsorbs>90% of the CO2 from a simulated coal flue stream andexhibitsexceptional thermal and oxidative stability over the course of extensiveadsorption/desorption cycling, placing it among top-performing adsorbentsto date for CO2 capture from a coal flue gas. Spectroscopiccharacterization and van der Waals-corrected density functional theorycalculations indicate that diamine-Mg-2(olz) materialscapture CO2 via the formation of ammonium carbamate chains.These results point more broadly to the opportunity for fundamentallyadvancing materials in this class through judicious design.
引用
收藏
页码:17151 / 17163
页数:13
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