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Title: Record-Setting Sorbents for Reversible Water Uptake by Systematic Anion Exchanges in Metal–Organic Frameworks

Abstract

The reversible capture of water vapor at low humidity can enable transformative applications such as atmospheric water harvesting and heat transfer that uses water as a refrigerant, replacing environmentally detrimental hydro- and chloro-fluorocarbons. The driving force for these applications is governed by the relative humidity at which the pores of a porous material fill with water. Here, we demonstrate modulation of the onset of pore-filling in a family of metal-organic frameworks with record water sorption capacities by employing anion exchange. Unexpectedly, the replacement of the structural bridging Cl- with the more hydrophilic anions F- and OH- does not induce porefilling at lower relative humidity, whereas the introduction of the larger Br- results in a substantial shift toward lower relative humidity. We rationalize these results in terms of pore size modifications as well as the water hydrogen bonding structure based on detailed infrared spectroscopic measurements. Fundamentally, our data suggest that, in the presence of strong nucleation sites, the thermodynamic favorability of water pore-filling depends more strongly on the pore diameter and the interface between water in the center of the pore and water bound to the pore walls than the hydrophilicity of the pore wall itself. On the basis of thesemore » results, we report two materials that exhibit record water uptake capacities in their respective humidity regions and extended stability over 400 water adsorption-desorption cycles.« less

Authors:
ORCiD logo [1]; ORCiD logo [1];  [1];  [1]; ORCiD logo [2]; ORCiD logo [1]
  1. Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Chemistry
  2. Univ. of Oregon, Eugene, OR (United States). Dept. of Chemistry and Biochemistry
Publication Date:
Research Org.:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Contributing Org.:
Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
OSTI Identifier:
1560063
Grant/Contract Number:  
AC02-06CH11357
Resource Type:
Accepted Manuscript
Journal Name:
Journal of the American Chemical Society
Additional Journal Information:
Journal Volume: 141; Journal Issue: 35; Journal ID: ISSN 0002-7863
Publisher:
American Chemical Society (ACS)
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY

Citation Formats

Rieth, Adam J., Wright, Ashley M., Skorupskii, Grigorii, Mancuso, Jenna L., Hendon, Christopher H., and Dincă, Mircea. Record-Setting Sorbents for Reversible Water Uptake by Systematic Anion Exchanges in Metal–Organic Frameworks. United States: N. p., 2019. Web. doi:10.1021/jacs.9b06246.
Rieth, Adam J., Wright, Ashley M., Skorupskii, Grigorii, Mancuso, Jenna L., Hendon, Christopher H., & Dincă, Mircea. Record-Setting Sorbents for Reversible Water Uptake by Systematic Anion Exchanges in Metal–Organic Frameworks. United States. https://doi.org/10.1021/jacs.9b06246
Rieth, Adam J., Wright, Ashley M., Skorupskii, Grigorii, Mancuso, Jenna L., Hendon, Christopher H., and Dincă, Mircea. Fri . "Record-Setting Sorbents for Reversible Water Uptake by Systematic Anion Exchanges in Metal–Organic Frameworks". United States. https://doi.org/10.1021/jacs.9b06246. https://www.osti.gov/servlets/purl/1560063.
@article{osti_1560063,
title = {Record-Setting Sorbents for Reversible Water Uptake by Systematic Anion Exchanges in Metal–Organic Frameworks},
author = {Rieth, Adam J. and Wright, Ashley M. and Skorupskii, Grigorii and Mancuso, Jenna L. and Hendon, Christopher H. and Dincă, Mircea},
abstractNote = {The reversible capture of water vapor at low humidity can enable transformative applications such as atmospheric water harvesting and heat transfer that uses water as a refrigerant, replacing environmentally detrimental hydro- and chloro-fluorocarbons. The driving force for these applications is governed by the relative humidity at which the pores of a porous material fill with water. Here, we demonstrate modulation of the onset of pore-filling in a family of metal-organic frameworks with record water sorption capacities by employing anion exchange. Unexpectedly, the replacement of the structural bridging Cl- with the more hydrophilic anions F- and OH- does not induce porefilling at lower relative humidity, whereas the introduction of the larger Br- results in a substantial shift toward lower relative humidity. We rationalize these results in terms of pore size modifications as well as the water hydrogen bonding structure based on detailed infrared spectroscopic measurements. Fundamentally, our data suggest that, in the presence of strong nucleation sites, the thermodynamic favorability of water pore-filling depends more strongly on the pore diameter and the interface between water in the center of the pore and water bound to the pore walls than the hydrophilicity of the pore wall itself. On the basis of these results, we report two materials that exhibit record water uptake capacities in their respective humidity regions and extended stability over 400 water adsorption-desorption cycles.},
doi = {10.1021/jacs.9b06246},
journal = {Journal of the American Chemical Society},
number = 35,
volume = 141,
place = {United States},
year = {Fri Aug 09 00:00:00 EDT 2019},
month = {Fri Aug 09 00:00:00 EDT 2019}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record

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Cited by: 71 works
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Figures / Tables:

Figure 1 Figure 1: Structure of Ni2X2BTDD (X = Cl, F, Br, OH). Left: View parallel to the c axis. Right: View of anion-exchanged SBUs perpendicular to the c axis and synthetic pathways.

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Evaluation of alternative refrigerant—adsorbent pairs for refrigeration cycles
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journal, January 2018


Effect of functional groups in MIL-101 on water sorption behavior
journal, July 2012


Adsorption-Based Atmospheric Water Harvesting: Impact of Material and Component Properties on System-Level Performance
journal, May 2019


Synthesis of Highly Crystalline NH 2 -MIL-125 (Ti) with S-Shaped Water Isotherms for Adsorption Heat Transformation
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journal, February 2017


AlPO-78: A 24-Layer ABC-6 Aluminophosphate Synthesized Using a Simple Structure-Directing Agent
journal, January 2018


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journal, October 2015

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Infrared Spectroscopy of Protonated Phenol–Water Clusters
journal, June 2018


Metal–Organic Frameworks in Adsorption-Driven Heat Pumps: The Potential of Alcohols as Working Fluids
journal, November 2015


Tuning Water Sorption in Highly Stable Zr(IV)-Metal–Organic Frameworks through Local Functionalization of Metal Clusters
journal, July 2018

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Record Atmospheric Fresh Water Capture and Heat Transfer with a Material Operating at the Water Uptake Reversibility Limit
journal, May 2017


Water Sorption Cycle Measurements on Functionalized MIL-101Cr for Heat Transformation Application
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journal, January 1951

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Unusual Hydrogen Bonding in Water-Filled Carbon Nanotubes
journal, September 2006

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  • DOI: 10.1021/ja057856u

Water Adsorption in Porous Metal–Organic Frameworks and Related Materials
journal, March 2014

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  • Journal of the American Chemical Society, Vol. 136, Issue 11, p. 4369-4381
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Water in Carbon Nanotubes: The Peculiar Hydrogen Bond Network Revealed by Infrared Spectroscopy
journal, August 2016

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  • Journal of the American Chemical Society, Vol. 138, Issue 33
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High and Reversible Ammonia Uptake in Mesoporous Azolate Metal–Organic Frameworks with Open Mn, Co, and Ni Sites
journal, July 2016

  • Rieth, Adam J.; Tulchinsky, Yuri; Dincă, Mircea
  • Journal of the American Chemical Society, Vol. 138, Issue 30
  • DOI: 10.1021/jacs.6b05723

Controlled Gas Uptake in Metal–Organic Frameworks with Record Ammonia Sorption
journal, February 2018

  • Rieth, Adam J.; Dincă, Mircea
  • Journal of the American Chemical Society, Vol. 140, Issue 9
  • DOI: 10.1021/jacs.8b00313

Tunable Metal–Organic Frameworks Enable High-Efficiency Cascaded Adsorption Heat Pumps
journal, November 2018

  • Rieth, Adam J.; Wright, Ashley M.; Rao, Sameer
  • Journal of the American Chemical Society, Vol. 140, Issue 50
  • DOI: 10.1021/jacs.8b09655

Reticular Access to Highly Porous acs -MOFs with Rigid Trigonal Prismatic Linkers for Water Sorption
journal, February 2019

  • Chen, Zhijie; Li, Penghao; Zhang, Xuan
  • Journal of the American Chemical Society, Vol. 141, Issue 7
  • DOI: 10.1021/jacs.8b13710

Application of Large Pore MCM-41 Molecular Sieves To Improve Pore Size Analysis Using Nitrogen Adsorption Measurements
journal, November 1997

  • Kruk, M.; Jaroniec, M.; Sayari, A.
  • Langmuir, Vol. 13, Issue 23
  • DOI: 10.1021/la970776m

Formation of ordered ice nanotubes inside carbon nanotubes
journal, August 2001

  • Koga, Kenichiro; Gao, G. T.; Tanaka, Hideki
  • Nature, Vol. 412, Issue 6849
  • DOI: 10.1038/35090532

Water structural transformation at molecular hydrophobic interfaces
journal, November 2012

  • Davis, Joel G.; Gierszal, Kamil P.; Wang, Ping
  • Nature, Vol. 491, Issue 7425
  • DOI: 10.1038/nature11570

Adsorption-based atmospheric water harvesting device for arid climates
journal, March 2018


A robust large-pore zirconium carboxylate metal–organic framework for energy-efficient water-sorption-driven refrigeration
journal, October 2018


Postsynthetic tuning of hydrophilicity in pyrazolate MOFs to modulate water adsorption properties
journal, January 2013

  • Wade, Casey R.; Corrales-Sanchez, Tachmajal; Narayan, Tarun C.
  • Energy & Environmental Science, Vol. 6, Issue 7
  • DOI: 10.1039/c3ee40876k

The Chemistry and Applications of Metal-Organic Frameworks
journal, August 2013

  • Furukawa, H.; Cordova, K. E.; O'Keeffe, M.
  • Science, Vol. 341, Issue 6149, p. 1230444-1230444
  • DOI: 10.1126/science.1230444

Fast elementary steps in chemical reaction mechanisms
journal, January 1963


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A Hydrolytically Stable Vanadium(IV) Metal–Organic Framework with Photocatalytic Bacteriostatic Activity for Autonomous Indoor Humidity Control
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Figures/Tables have been extracted from DOE-funded journal article accepted manuscripts.