Selective Vapor Pressure Dependent Proton Transport in a Metal-Organic Framework with Two Distinct Hydrophilic Pores

The mechanism of proton conductivity in porous solids (i.e., Grotthuss or vehicular) is related to the structure and chemical environment of the pores. Direct observation of structure-function relationships is difficult because state-of-the-art solid proton conductors are often amorphous. Here, we p...

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Bibliographic Details
Main Authors: Park, Sarah Sunah (Author), Rieth, Adam Joseph (Author), Hendon, Christopher H (Author), Dinca, Mircea (Author)
Other Authors: Massachusetts Institute of Technology. Department of Chemistry (Contributor)
Format: Article
Language:English
Published: American Chemical Society (ACS), 2020-07-13T16:21:17Z.
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042 |a dc 
100 1 0 |a Park, Sarah Sunah  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Chemistry  |e contributor 
700 1 0 |a Rieth, Adam Joseph  |e author 
700 1 0 |a Hendon, Christopher H  |e author 
700 1 0 |a Dinca, Mircea  |e author 
245 0 0 |a Selective Vapor Pressure Dependent Proton Transport in a Metal-Organic Framework with Two Distinct Hydrophilic Pores 
260 |b American Chemical Society (ACS),   |c 2020-07-13T16:21:17Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/126155 
520 |a The mechanism of proton conductivity in porous solids (i.e., Grotthuss or vehicular) is related to the structure and chemical environment of the pores. Direct observation of structure-function relationships is difficult because state-of-the-art solid proton conductors are often amorphous. Here, we present a systematic elucidation of two distinct proton transport pathways within MIT-25, a mesoporous metal-organic framework that exhibits parallel channels of ∼27 Å and ∼4.5 Å width. We characterize transport through these pores using temperature- and humidity-dependent proton conductivity measurements and density functional theory. Through control of vapor pressure we are able to sequentially fill the small and large pores, promoting proton conductivity with distinct activation energies at low and high relative humidity, respectively. 
520 |a U.S. Department of Energy, Office of Basic Energy Sciences (grant no. DE-SC0018235) 
520 |a NSF (grant no. ACI-1053575) 
520 |a NSF GRFP (grant no. 1122374) 
546 |a en 
655 7 |a Article 
773 |t 10.1021/JACS.7B12784 
773 |t Journal of the American Chemical Society