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Title: Phenyl/Perfluorophenyl Stacking Interactions Enhance Structural Order in Two-Dimensional Covalent Organic Frameworks

Abstract

A two-dimensional imine-based covalent organic framework (COF) was designed and synthesized such that phenyl and perfluorophenyl structural units can seamlessly alternate between layers of the framework. X-ray diffraction of the COF powders reveals a striking increase in crystallinity for the COF with self-complementary phenyl/perfluorophenyl interactions (FASt-COF). Whereas measured values of the Brunauer-Emmet-Teller (BET) surface areas for the nonfluorinated Base-COF and the COF employing hydrogen bonding were ~37% and 59%, respectively, of their theoretical Connolly surface areas, the BET value for FASt-COF achieves >90% of its theoretical value (~1700 m2/g). Transmission electron microscopy images also revealed unique micron-sized rodlike features in FASt-COF that were not present in the other materials. The results highlight a promising approach for improving surface areas and long-range order in two-dimensional COFs.

Authors:
ORCiD logo [1];  [1];  [2];  [1];  [3];  [1];  [4]; ORCiD logo [4]; ORCiD logo [1]
  1. National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States
  2. Quantum Simulations Group, Lawrence Livermore National Laboratory, Livermore, California 94550, United States
  3. National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, United States
  4. Department of Chemistry, Colorado School of Mines, 1012 14th Street, Golden, Colorado 80401, United States
Publication Date:
Research Org.:
National Renewable Energy Lab. (NREL), Golden, CO (United States)
Sponsoring Org.:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Fuel Cell Technologies Office (EE-3F)
OSTI Identifier:
1457122
Report Number(s):
NREL/JA-5900-70871
Journal ID: ISSN 1528-7483
DOE Contract Number:
AC36-08GO28308
Resource Type:
Journal Article
Resource Relation:
Journal Name: Crystal Growth and Design; Journal Volume: 18; Journal Issue: 7
Country of Publication:
United States
Language:
English
Subject:
36 MATERIALS SCIENCE; frameworks; gas storage; crystal; fluorination

Citation Formats

Braunecker, Wade A., Hurst, Katherine E., Ray, Keith G., Owczarczyk, Zbyslaw R., Martinez, Madison B., Leick, Noemi, Keuhlen, Amy, Sellinger, Alan, and Johnson, Justin C. Phenyl/Perfluorophenyl Stacking Interactions Enhance Structural Order in Two-Dimensional Covalent Organic Frameworks. United States: N. p., 2018. Web. doi:10.1021/acs.cgd.8b00630.
Braunecker, Wade A., Hurst, Katherine E., Ray, Keith G., Owczarczyk, Zbyslaw R., Martinez, Madison B., Leick, Noemi, Keuhlen, Amy, Sellinger, Alan, & Johnson, Justin C. Phenyl/Perfluorophenyl Stacking Interactions Enhance Structural Order in Two-Dimensional Covalent Organic Frameworks. United States. doi:10.1021/acs.cgd.8b00630.
Braunecker, Wade A., Hurst, Katherine E., Ray, Keith G., Owczarczyk, Zbyslaw R., Martinez, Madison B., Leick, Noemi, Keuhlen, Amy, Sellinger, Alan, and Johnson, Justin C. Mon . "Phenyl/Perfluorophenyl Stacking Interactions Enhance Structural Order in Two-Dimensional Covalent Organic Frameworks". United States. doi:10.1021/acs.cgd.8b00630.
@article{osti_1457122,
title = {Phenyl/Perfluorophenyl Stacking Interactions Enhance Structural Order in Two-Dimensional Covalent Organic Frameworks},
author = {Braunecker, Wade A. and Hurst, Katherine E. and Ray, Keith G. and Owczarczyk, Zbyslaw R. and Martinez, Madison B. and Leick, Noemi and Keuhlen, Amy and Sellinger, Alan and Johnson, Justin C.},
abstractNote = {A two-dimensional imine-based covalent organic framework (COF) was designed and synthesized such that phenyl and perfluorophenyl structural units can seamlessly alternate between layers of the framework. X-ray diffraction of the COF powders reveals a striking increase in crystallinity for the COF with self-complementary phenyl/perfluorophenyl interactions (FASt-COF). Whereas measured values of the Brunauer-Emmet-Teller (BET) surface areas for the nonfluorinated Base-COF and the COF employing hydrogen bonding were ~37% and 59%, respectively, of their theoretical Connolly surface areas, the BET value for FASt-COF achieves >90% of its theoretical value (~1700 m2/g). Transmission electron microscopy images also revealed unique micron-sized rodlike features in FASt-COF that were not present in the other materials. The results highlight a promising approach for improving surface areas and long-range order in two-dimensional COFs.},
doi = {10.1021/acs.cgd.8b00630},
journal = {Crystal Growth and Design},
number = 7,
volume = 18,
place = {United States},
year = {Mon May 21 00:00:00 EDT 2018},
month = {Mon May 21 00:00:00 EDT 2018}
}