Promotion of Proton Conductivity by Encapsulation of Metal‐Organic Polyhedra in Metal‐Organic Frameworks
A Zr‐based metal‐organic polyhedron (MOP) was self‐assembled in a porous MOF host, DUT‐68, successfully to synthesize MOP‐1@DUT‐68. The MOP guest (MOP‐1) has a diameter of about 20 Å, larger than that of the square windows (pore sizes of ∼14 Å) of DUT‐68 but smaller than that of the rhombicuboctahed...
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Published in | Chemistry : a European journal Vol. 27; no. 47; pp. 12137 - 12143 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
19.08.2021
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Subjects | |
Online Access | Get full text |
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Summary: | A Zr‐based metal‐organic polyhedron (MOP) was self‐assembled in a porous MOF host, DUT‐68, successfully to synthesize MOP‐1@DUT‐68. The MOP guest (MOP‐1) has a diameter of about 20 Å, larger than that of the square windows (pore sizes of ∼14 Å) of DUT‐68 but smaller than that of the rhombicuboctahedral cage (27.7 Å), which means that the migration and leaching of MOP‐1 could be effectively prohibited if MOP‐1 is encapsulated in the MOF′s cavities. The proton conductivity of MOP‐1@DUT‐68 is 1.14×10−3 S cm−1 (at 80 °C under 98 % relative humidity), which is three orders of magnitude higher than that of DUT‐68. Compared with MOP‐1⊂DUT‐68, which was synthesized by impregnation, MOP‐1@DUT‐68 is more prone to form faster proton‐conduction pathways and thus provides higher proton conductivity.
Protons get a move on: A Zr‐based metal‐organic polyhedron (MOP‐1) was self‐assembled in a porous MOF host, DUT‐68, to synthesize MOP‐1@DUT‐68. The migration and leaching of MOP could be effectively prohibited if MOP‐1 was encapsulated in the MOF′s cavities. Incorporation of MOP‐1 makes the proton conductivity of MOP‐1@DUT‐68 reach 1.14×10−3 S cm−1 (at 80 °C under 98 % RH), which is three orders of magnitude higher than that of DUT‐68. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0947-6539 1521-3765 1521-3765 |
DOI: | 10.1002/chem.202101213 |