메뉴 건너뛰기




Volumn 28, Issue 5, 2016, Pages 1489-1494

Interplaying Intrinsic and Extrinsic Proton Conductivities in Covalent Organic Frameworks

Author keywords

[No Author keywords available]

Indexed keywords

MOLECULES; SYNTHESIS (CHEMICAL);

EID: 84960375734     PISSN: 08974756     EISSN: 15205002     Source Type: Journal    
DOI: 10.1021/acs.chemmater.5b04947     Document Type: Article
Times cited : (347)

References (40)
  • 1
    • 34548688889 scopus 로고    scopus 로고
    • The United States Department of Energy's high temperature, low relative humidity membrane program
    • Garland, N.; Kopasz, J. P. The United States Department of Energy's high temperature, low relative humidity membrane program J. Power Sources 2007, 172, 94-99 10.1016/j.jpowsour.2007.01.025
    • (2007) J. Power Sources , vol.172 , pp. 94-99
    • Garland, N.1    Kopasz, J.P.2
  • 2
    • 0347418166 scopus 로고    scopus 로고
    • Approaches and Recent Development of Polymer Electrolyte Membranes for Fuel Cells Operating above 100°C
    • Li, Q.; He, R.; Jensen, J. O.; Bjerrum, N. J. Approaches and Recent Development of Polymer Electrolyte Membranes for Fuel Cells Operating above 100°C Chem. Mater. 2003, 15, 4896-4915 10.1021/cm0310519
    • (2003) Chem. Mater. , vol.15 , pp. 4896-4915
    • Li, Q.1    He, R.2    Jensen, J.O.3    Bjerrum, N.J.4
  • 3
    • 7644219892 scopus 로고    scopus 로고
    • State of understanding of Nafion
    • Mauritz, K. A.; Moore, R. B. State of understanding of Nafion Chem. Rev. 2004, 104, 4535-4585 10.1021/cr0207123
    • (2004) Chem. Rev. , vol.104 , pp. 4535-4585
    • Mauritz, K.A.1    Moore, R.B.2
  • 5
    • 70350450369 scopus 로고    scopus 로고
    • Sulfonated aromatic hydrocarbon polymers as proton exchange membranes for fuel cells
    • Higashihara, T.; Matsumoto, K.; Ueda, M. Sulfonated aromatic hydrocarbon polymers as proton exchange membranes for fuel cells Polymer 2009, 50, 5341-5357 10.1016/j.polymer.2009.09.001
    • (2009) Polymer , vol.50 , pp. 5341-5357
    • Higashihara, T.1    Matsumoto, K.2    Ueda, M.3
  • 6
    • 67651224880 scopus 로고    scopus 로고
    • Rational Designs for Highly Proton-Conductive Metal-Organic Frameworks
    • Sadakiyo, M.; Yamada, T.; Kitagawa, H. Rational Designs for Highly Proton-Conductive Metal-Organic Frameworks J. Am. Chem. Soc. 2009, 131, 9906-9907 10.1021/ja9040016
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 9906-9907
    • Sadakiyo, M.1    Yamada, T.2    Kitagawa, H.3
  • 7
    • 84888610789 scopus 로고    scopus 로고
    • Ion Conductivity and Transport by Porous Coordination Polymers and Metal-Organic Frameworks
    • Horike, S.; Umeyama, D.; Kitagawa, S. Ion Conductivity and Transport by Porous Coordination Polymers and Metal-Organic Frameworks Acc. Chem. Res. 2013, 46, 2376-2384 10.1021/ar300291s
    • (2013) Acc. Chem. Res. , vol.46 , pp. 2376-2384
    • Horike, S.1    Umeyama, D.2    Kitagawa, S.3
  • 8
    • 84874643448 scopus 로고    scopus 로고
    • Proton Conduction in Metal-Organic Frameworks and Related Modularly Built Porous Solids
    • Yoon, M.; Suh, K.; Natarajan, S.; Kim, K. Proton Conduction in Metal-Organic Frameworks and Related Modularly Built Porous Solids Angew. Chem., Int. Ed. 2013, 52, 2688-2700 10.1002/anie.201206410
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2688-2700
    • Yoon, M.1    Suh, K.2    Natarajan, S.3    Kim, K.4
  • 9
    • 84880713504 scopus 로고    scopus 로고
    • Proton Conduction with Metal-Organic Frameworks
    • Shimizu, G. K. H.; Taylor, J. M.; Kim, S. R. Proton Conduction with Metal-Organic Frameworks Science 2013, 341, 354-355 10.1126/science.1239872
    • (2013) Science , vol.341 , pp. 354-355
    • Shimizu, G.K.H.1    Taylor, J.M.2    Kim, S.R.3
  • 10
    • 84903701555 scopus 로고    scopus 로고
    • MOFs as proton conductors-Challenges and opportunities
    • Ramaswamy, P.; Wong, N. E.; Shimizu, G. K. H. MOFs as proton conductors-Challenges and opportunities Chem. Soc. Rev. 2014, 43, 5913-5932 10.1039/C4CS00093E
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 5913-5932
    • Ramaswamy, P.1    Wong, N.E.2    Shimizu, G.K.H.3
  • 11
    • 84927722973 scopus 로고    scopus 로고
    • Superprotonic Conductivity of a UiO-66 Framework Functionalized with Sulfonic Acid Groups by Facile Postsynthetic Oxidation
    • Phang, W. J.; Jo, H.; Lee, W. R.; Song, J. H.; Yoo, K.; Kim, B.; Hong, C. S. Superprotonic Conductivity of a UiO-66 Framework Functionalized with Sulfonic Acid Groups by Facile Postsynthetic Oxidation Angew. Chem., Int. Ed. 2015, 54, 5142-5146 10.1002/anie.201411703
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 5142-5146
    • Phang, W.J.1    Jo, H.2    Lee, W.R.3    Song, J.H.4    Yoo, K.5    Kim, B.6    Hong, C.S.7
  • 12
    • 84943664092 scopus 로고    scopus 로고
    • Synthesis of a Sulfonated Two-Dimensional Covalent Organic Framework as an Efficient Solid Acid Catalyst for Biobased Chemical Conversion
    • Peng, Y.; Hu, Z.; Gao, Y.; Yuan, D.; Kang, Z.; Qian, Y.; Yan, N.; Zhao, D. Synthesis of a Sulfonated Two-Dimensional Covalent Organic Framework as an Efficient Solid Acid Catalyst for Biobased Chemical Conversion ChemSusChem 2015, 8, 3208-3212 10.1002/cssc.201500755
    • (2015) ChemSusChem , vol.8 , pp. 3208-3212
    • Peng, Y.1    Hu, Z.2    Gao, Y.3    Yuan, D.4    Kang, Z.5    Qian, Y.6    Yan, N.7    Zhao, D.8
  • 13
    • 70349327378 scopus 로고    scopus 로고
    • One-dimensional imidazole aggregate in aluminium porous coordination polymers with high proton conductivity
    • Bureekaew, S.; Horike, S.; Higuchi, M.; Mizuno, M.; Kawamura, T.; Tanaka, D.; Yanai, N.; Kitagawa, S. One-dimensional imidazole aggregate in aluminium porous coordination polymers with high proton conductivity Nat. Mater. 2009, 8, 831-836 10.1038/nmat2526
    • (2009) Nat. Mater. , vol.8 , pp. 831-836
    • Bureekaew, S.1    Horike, S.2    Higuchi, M.3    Mizuno, M.4    Kawamura, T.5    Tanaka, D.6    Yanai, N.7    Kitagawa, S.8
  • 14
    • 82455192767 scopus 로고    scopus 로고
    • Confinement of Mobile Histamine in Coordination Nanochannels for Fast Proton Transfer
    • Umeyama, D.; Horike, S.; Inukai, M.; Hijikata, Y.; Kitagawa, S. Confinement of Mobile Histamine in Coordination Nanochannels for Fast Proton Transfer Angew. Chem., Int. Ed. 2011, 50, 11706-11709 10.1002/anie.201102997
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 11706-11709
    • Umeyama, D.1    Horike, S.2    Inukai, M.3    Hijikata, Y.4    Kitagawa, S.5
  • 15
    • 84866715758 scopus 로고    scopus 로고
    • Imparting High Proton Conductivity to a Metal-Organic Framework Material by Controlled Acid Impregnation
    • Ponomareva, V. G.; Kovalenko, K. A.; Chupakhin, A. P.; Dybtsev, D. N.; Shutova, E. S.; Fedin, V. P. Imparting High Proton Conductivity to a Metal-Organic Framework Material by Controlled Acid Impregnation J. Am. Chem. Soc. 2012, 134, 15640-15643 10.1021/ja305587n
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 15640-15643
    • Ponomareva, V.G.1    Kovalenko, K.A.2    Chupakhin, A.P.3    Dybtsev, D.N.4    Shutova, E.S.5    Fedin, V.P.6
  • 16
    • 84903529723 scopus 로고    scopus 로고
    • Enhanced Proton Conductivity of Nafion Hybrid Membrane under Different Humidities by Incorporating Metal-Organic Frameworks with High Phytic Acid Loading
    • Li, Z.; He, G.; Zhang, B.; Cao, Y.; Wu, H.; Jiang, Z.; Tiantian, Z. Enhanced Proton Conductivity of Nafion Hybrid Membrane under Different Humidities by Incorporating Metal-Organic Frameworks with High Phytic Acid Loading ACS Appl. Mater. Interfaces 2014, 6, 9799-9807 10.1021/am502236v
    • (2014) ACS Appl. Mater. Interfaces , vol.6 , pp. 9799-9807
    • Li, Z.1    He, G.2    Zhang, B.3    Cao, Y.4    Wu, H.5    Jiang, Z.6    Tiantian, Z.7
  • 17
    • 80455129359 scopus 로고    scopus 로고
    • Helical Water Chain Mediated Proton Conductivity in Homochiral Metal-Organic Frameworks with Unprecedented Zeolitic unh-Topology
    • Sahoo, S. C.; Kundu, T.; Banerjee, R. Helical Water Chain Mediated Proton Conductivity in Homochiral Metal-Organic Frameworks with Unprecedented Zeolitic unh-Topology J. Am. Chem. Soc. 2011, 133, 17950-17958 10.1021/ja2078637
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 17950-17958
    • Sahoo, S.C.1    Kundu, T.2    Banerjee, R.3
  • 19
    • 84860872207 scopus 로고    scopus 로고
    • Coordination-Network-Based Ionic Plastic Crystal for Anhydrous Proton Conductivity
    • Horike, S.; Umeyama, D.; Inukai, M.; Itakura, T.; Kitagawa, S. Coordination-Network-Based Ionic Plastic Crystal for Anhydrous Proton Conductivity J. Am. Chem. Soc. 2012, 134, 7612-7615 10.1021/ja301875x
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 7612-7615
    • Horike, S.1    Umeyama, D.2    Inukai, M.3    Itakura, T.4    Kitagawa, S.5
  • 20
    • 84881035738 scopus 로고    scopus 로고
    • Integration of Intrinsic Proton Conduction and Guest-Accessible Nanospace into a Coordination Polymer
    • Umeyama, D.; Horike, S.; Inukai, M.; Kitagawa, S. Integration of Intrinsic Proton Conduction and Guest-Accessible Nanospace into a Coordination Polymer J. Am. Chem. Soc. 2013, 135, 11345-11350 10.1021/ja4051668
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 11345-11350
    • Umeyama, D.1    Horike, S.2    Inukai, M.3    Kitagawa, S.4
  • 22
    • 84921484872 scopus 로고    scopus 로고
    • High Anhydrous Proton Conductivity of Imidazole-Loaded Mesoporous Polyimides over a Wide Range from Subzero to Moderate Temperature
    • Ye, Y.; Zhang, L.; Peng, Q.; Wang, G. E.; Shen, Y.; Li, Z.; Wang, L.; Ma, X.; Chen, Q. H.; Zhang, Z.; Xiang, S. High Anhydrous Proton Conductivity of Imidazole-Loaded Mesoporous Polyimides over a Wide Range from Subzero to Moderate Temperature J. Am. Chem. Soc. 2015, 137, 913-918 10.1021/ja511389q
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 913-918
    • Ye, Y.1    Zhang, L.2    Peng, Q.3    Wang, G.E.4    Shen, Y.5    Li, Z.6    Wang, L.7    Ma, X.8    Chen, Q.H.9    Zhang, Z.10    Xiang, S.11
  • 24
    • 0000344783 scopus 로고
    • High Protonic Conduction of Polybenzlmldazole Films
    • Hoel, D.; Grunwald, E. High Protonic Conduction of Polybenzlmldazole Films J. Phys. Chem. 1977, 81, 2135-2136 10.1021/j100537a021
    • (1977) J. Phys. Chem. , vol.81 , pp. 2135-2136
    • Hoel, D.1    Grunwald, E.2
  • 25
    • 0035912173 scopus 로고    scopus 로고
    • Solid acids as fuel cell electrolytes
    • Haile, S. M.; Boysen, D. A.; Chisholm, C. R. I.; Merle, R. B. Solid acids as fuel cell electrolytes Nature 2001, 410, 910-913 10.1038/35073536
    • (2001) Nature , vol.410 , pp. 910-913
    • Haile, S.M.1    Boysen, D.A.2    Chisholm, C.R.I.3    Merle, R.B.4
  • 27
    • 65349161535 scopus 로고    scopus 로고
    • Phosphonate and sulfonate metal organic frameworks
    • Shimizu, G. K. H.; Vaidhyanathan, R.; Taylor, J. M. Phosphonate and sulfonate metal organic frameworks Chem. Soc. Rev. 2009, 38, 1430-1449 10.1039/b802423p
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 1430-1449
    • Shimizu, G.K.H.1    Vaidhyanathan, R.2    Taylor, J.M.3
  • 28
    • 84864473297 scopus 로고    scopus 로고
    • Inherent Proton Conduction in a 2D Coordination Framework
    • Umeyama, D.; Horike, S.; Inukai, M.; Itakura, T.; Kitagawa, S. Inherent Proton Conduction in a 2D Coordination Framework J. Am. Chem. Soc. 2012, 134, 12780-12785 10.1021/ja304693r
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 12780-12785
    • Umeyama, D.1    Horike, S.2    Inukai, M.3    Itakura, T.4    Kitagawa, S.5
  • 29
    • 84908542948 scopus 로고    scopus 로고
    • Intrinsic and extrinsic proton conductivity in metal-organic frameworks
    • Tominaka, S.; Cheetham, A. K. Intrinsic and extrinsic proton conductivity in metal-organic frameworks RSC Adv. 2014, 4, 54382-54387 10.1039/C4RA11473F
    • (2014) RSC Adv. , vol.4 , pp. 54382-54387
    • Tominaka, S.1    Cheetham, A.K.2
  • 30
    • 84891307740 scopus 로고    scopus 로고
    • Highly proton conductive nanoporous coordination polymers with sulfonic acid groups on the pore surface
    • Ramaswamy, P.; Matsuda, R.; Kosaka, W.; Akiyama, G.; Jeon, H. J.; Kitagawa, S. Highly proton conductive nanoporous coordination polymers with sulfonic acid groups on the pore surface Chem. Commun. 2014, 50, 1144-1146 10.1039/C3CC47980C
    • (2014) Chem. Commun. , vol.50 , pp. 1144-1146
    • Ramaswamy, P.1    Matsuda, R.2    Kosaka, W.3    Akiyama, G.4    Jeon, H.J.5    Kitagawa, S.6
  • 32
    • 84879109916 scopus 로고    scopus 로고
    • Rationally synthesized two-dimensional polymers
    • Colson, J. W.; Dichtel, W. R. Rationally synthesized two-dimensional polymers Nat. Chem. 2013, 5, 453-465 10.1038/nchem.1628
    • (2013) Nat. Chem. , vol.5 , pp. 453-465
    • Colson, J.W.1    Dichtel, W.R.2
  • 33
    • 84879109916 scopus 로고    scopus 로고
    • Rationally synthesized two-dimensional polymers
    • Colson, J. W.; Dichtel, W. R. Rationally synthesized two-dimensional polymers Nat. Chem. 2013, 5, 453-465 10.1038/nchem.1628
    • (2013) Nat. Chem. , vol.5 , pp. 453-465
    • Colson, J.W.1    Dichtel, W.R.2
  • 34
    • 85027923814 scopus 로고    scopus 로고
    • Two-Dimensional Covalent Organic Frameworks for Carbon Dioxide Capture through Channel-Wall Functionalization
    • Huang, N.; Chen, X.; Krishna, R.; Jiang, D. Two-Dimensional Covalent Organic Frameworks for Carbon Dioxide Capture through Channel-Wall Functionalization Angew. Chem., Int. Ed. 2015, 54, 2986-2990 10.1002/anie.201411262
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 2986-2990
    • Huang, N.1    Chen, X.2    Krishna, R.3    Jiang, D.4
  • 35
    • 83055165872 scopus 로고    scopus 로고
    • Construction of Covalent Organic Framework for Catalysis: Pd/COF-LZU1 in Suzuki-Miyaura Coupling Reaction
    • Ding, S. Y.; Gao, J.; Wang, Q.; Zhang, Y.; Song, W.; Su, C.; Wang, W. Construction of Covalent Organic Framework for Catalysis: Pd/COF-LZU1 in Suzuki-Miyaura Coupling Reaction J. Am. Chem. Soc. 2011, 133, 19816-19822 10.1021/ja206846p
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19816-19822
    • Ding, S.Y.1    Gao, J.2    Wang, Q.3    Zhang, Y.4    Song, W.5    Su, C.6    Wang, W.7
  • 36
    • 84874602290 scopus 로고    scopus 로고
    • A Photoconductive Thienothiophene-Based Covalent Organic Framework Showing Charge Transfer Towards Included Fullerene
    • Dogru, M.; Handloser, M.; Auras, F.; Kunz, T.; Medina, D.; Hartschuh, A.; Knochel, P.; Bein, T. A Photoconductive Thienothiophene-Based Covalent Organic Framework Showing Charge Transfer Towards Included Fullerene Angew. Chem., Int. Ed. 2013, 52, 2920-2924 10.1002/anie.201208514
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2920-2924
    • Dogru, M.1    Handloser, M.2    Auras, F.3    Kunz, T.4    Medina, D.5    Hartschuh, A.6    Knochel, P.7    Bein, T.8
  • 37
    • 84870659680 scopus 로고    scopus 로고
    • Construction of Crystalline 2D Covalent Organic Frameworks with Remarkable Chemical (Acid/Base) Stability via a Combined Reversible and Irreversible Route
    • Kandambeth, S.; Mallick, A.; Lukose, B.; Mane, V. M.; Heine, T.; Banerjee, R. Construction of Crystalline 2D Covalent Organic Frameworks with Remarkable Chemical (Acid/Base) Stability via a Combined Reversible and Irreversible Route J. Am. Chem. Soc. 2012, 134, 19524-19527 10.1021/ja308278w
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 19524-19527
    • Kandambeth, S.1    Mallick, A.2    Lukose, B.3    Mane, V.M.4    Heine, T.5    Banerjee, R.6
  • 38
    • 84887653053 scopus 로고    scopus 로고
    • β-Ketoenamine-Linked Covalent Organic Frameworks Capable of Pseudocapacitive Energy Storage
    • DeBlase, C. R.; Silberstein, K. E.; Truong, T.-T.; Abrunã, H. D.; Dichtel, W. R. β-Ketoenamine-Linked Covalent Organic Frameworks Capable of Pseudocapacitive Energy Storage J. Am. Chem. Soc. 2013, 135, 16821-16824 10.1021/ja409421d
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 16821-16824
    • DeBlase, C.R.1    Silberstein, K.E.2    Truong, T.-T.3    Abrunã, H.D.4    Dichtel, W.R.5
  • 40
    • 84872513360 scopus 로고    scopus 로고
    • Control of Crystallinity and Porosity of Covalent Organic Frameworks by Managing Interlayer Interactions Based on Self-Complementary π-Electronic Force
    • Chen, X.; Addicoat, M.; Irle, S.; Nagai, A.; Jiang, D. Control of Crystallinity and Porosity of Covalent Organic Frameworks by Managing Interlayer Interactions Based on Self-Complementary π-Electronic Force J. Am. Chem. Soc. 2013, 135, 546-549 10.1021/ja3100319
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 546-549
    • Chen, X.1    Addicoat, M.2    Irle, S.3    Nagai, A.4    Jiang, D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.