TY - JOUR
T1 - Development of a Heat-Treated Polymer-Polymer Type Charge-Transfer Blend Membrane for Application in Polymer Electrolyte Fuel Cells
AU - Feng, Shiyan
AU - Kondo, Shoichi
AU - Kikuchi, Takamasa
AU - Christiani, Liana
AU - Hwang, Byungchan
AU - Sasaki, Kazunari
AU - Nishihara, Masamichi
N1 - Funding Information:
The authors gratefully acknowledge financial support by Grant-in-Aid for Scientific Research (C) (26410223), JSPS Japan, Center of Innovation Science and Technology based Radical Innovation and Entrepreneurship Program (COI Program, JPMJCE1318), JST Japan, and collaboration research with Nissan Chemical Corporation. We thank Prof. Stephen Lyth for checking this manuscript.
Funding Information:
The authors gratefully acknowledge financial support by Grant-in-Aid for Scientific Research (C) (26410223), JSPS Japan Center of Innovation Science and Technology based Radical Innovation and Entrepreneurship Program (COI Program, JPMJCE1318), JST Japan and collaboration research with Nissan Chemical Corporation. We thank Prof. Stephen Lyth for checking this manuscript.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/12/23
Y1 - 2019/12/23
N2 - We developed polymer electrolyte membranes (PEMs) utilizing charge-transfer (CT) interactions for polymer electrolyte fuel cells (PEFCs). CT complex formation was applied to control the position of proton conductive groups in the membranes. To understand the effect of CT complex formation on PEM performance, heat treatment was performed to enhance the extent of CT complex formation in the membrane. In this work, sulfonated polyimide (SPI) was used as the electron-accepting polymer, while polyether-containing electron-rich dialkoxynaphthalene (Poly-DAN) was used as the electron-donating polymer. After heat treatment at 150 °C for 50 h, the concentration of CT complex in the membrane was significantly enhanced by about 13 times. Heat-treated SPI/Poly-DAN membranes showed higher mechanical strength (50.8 MPa) than Nafion 212 (15.5 MPa) and highly chemical durability compared to the untreated membrane by the synergetic effect of enhanced CT complex formation and chemical cross-linking. Heat-treated SPI/Poly-DAN membranes also showed reasonable proton conductivity (32.3 mS cm-1, 80 °C, and 90% RH), although some cross-linking occurred between sulfonic acid units due to the heat treatment process. In single cell tests, heat-treated SPI/Poly-DAN membranes had maximum power densities of 255 mW cm-2 at 80 °C and 95% RH and 59.0 mW cm-2 at 110 °C and 31% RH, indicating that these heat-treated CT complex membranes could be used for fuel cell applications.
AB - We developed polymer electrolyte membranes (PEMs) utilizing charge-transfer (CT) interactions for polymer electrolyte fuel cells (PEFCs). CT complex formation was applied to control the position of proton conductive groups in the membranes. To understand the effect of CT complex formation on PEM performance, heat treatment was performed to enhance the extent of CT complex formation in the membrane. In this work, sulfonated polyimide (SPI) was used as the electron-accepting polymer, while polyether-containing electron-rich dialkoxynaphthalene (Poly-DAN) was used as the electron-donating polymer. After heat treatment at 150 °C for 50 h, the concentration of CT complex in the membrane was significantly enhanced by about 13 times. Heat-treated SPI/Poly-DAN membranes showed higher mechanical strength (50.8 MPa) than Nafion 212 (15.5 MPa) and highly chemical durability compared to the untreated membrane by the synergetic effect of enhanced CT complex formation and chemical cross-linking. Heat-treated SPI/Poly-DAN membranes also showed reasonable proton conductivity (32.3 mS cm-1, 80 °C, and 90% RH), although some cross-linking occurred between sulfonic acid units due to the heat treatment process. In single cell tests, heat-treated SPI/Poly-DAN membranes had maximum power densities of 255 mW cm-2 at 80 °C and 95% RH and 59.0 mW cm-2 at 110 °C and 31% RH, indicating that these heat-treated CT complex membranes could be used for fuel cell applications.
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U2 - 10.1021/acsaem.9b01697
DO - 10.1021/acsaem.9b01697
M3 - Article
AN - SCOPUS:85075614050
SN - 2574-0962
VL - 2
SP - 8715
EP - 8723
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 12
ER -