Porous Covalent Organic Polymers for Efficient Fluorocarbon-Based Adsorption Cooling

被引:26
|
作者
Zheng, Jian [1 ,5 ]
Wahiduzzaman, Mohammad [2 ]
Barpaga, Dushyant [3 ]
Trump, Benjamin A. [4 ]
Gutierrez, Oliver Y. [5 ]
Thallapally, Praveen [5 ]
Ma, Shengqian [6 ]
McGrail, B. Peter [3 ]
Maurin, Guillaume [2 ]
Motkuri, Radha Kishan [3 ]
机构
[1] Sichuan Univ, Dept Chem Engn, Chengdu 610065, Peoples R China
[2] Univ Montpellier, CNRS, ICGM, ENSCM, Montpellier, France
[3] Pacific Northwest Natl Lab, Energy & Environm Directorate, Richland, WA 99352 USA
[4] Natl Inst Stand & Technol, Ctr Neutron Diffract, Gaithersburg, MD 20899 USA
[5] Pacific Northwest Natl Lab, Phys & Computat Sci Directorate, Richland, WA 99352 USA
[6] Univ North Texas, Dept Chem, Denton, TX 76201 USA
关键词
adsorption cooling; structure defects; fluorocarbon refrigerants; porous covalent organic polymers; FRAMEWORKS; SORPTION; WATER; HYSTERESIS; CHEMISTRY; NETWORKS;
D O I
10.1002/anie.202102337
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Adsorption-based cooling is an energy-efficient renewable-energy technology that can be driven using low-grade industrial waste heat and/or solar heat. Here, we report the first exploration of fluorocarbon adsorption using porous covalent organic polymers (COPs) for this cooling application. High fluorocarbon R134a equilibrium capacities and unique overall linear-shaped isotherms are revealed for the materials, namely COP-2 and COP-3. The key role of mesoporous defects on this unusual adsorption behavior was demonstrated by molecular simulations based on atomistic defect-containing models built for both porous COPs. Analysis of simulated R134a adsorption isotherms for various defect-containing atomistic models of the COPs shows a direct correlation between higher fluorocarbon adsorption capacities and increasing pore volumes induced by defects. Combined with their high porosities, excellent reversibility, fast kinetics, and large operating window, these defect-containing porous COPs are promising for adsorption-based cooling applications.
引用
收藏
页码:18037 / 18043
页数:7
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