Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/75797
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Type: Journal article
Title: Hydrolytically stable phosphorylated hybrid silicas for proton conduction
Author: Jin, Y.
Qiao, S.
da Costa, J.
Wood, B.
Ladewig, B.
Lu, G.
Citation: Advanced Functional Materials, 2007; 17(16):3304-3311
Publisher: Wiley - VCH Verlag GmbH & Co
Issue Date: 2007
ISSN: 1616-301X
1616-3028
Statement of
Responsibility: 
Yonggang Jin, Shizhang Qiao, João C. Diniz da Costa, Barry J. Wood, Bradley P. Ladewig, and Gao Qing Lu
Abstract: <jats:title>Abstract</jats:title><jats:p>A new approach to the synthesis of fully immobilized phosphorus functionalized hybrid proton conductive gels based on phosphonic acid grafting is presented in this paper. The hybrid silicas with different amounts of phosphonic acid have been prepared and characterized using Fourier‐transform infrared spectroscopy, X‐ray photoelectron spectroscopy, Brunauer–Emmett–Teller surface area analysis, thermogravimetric analysis, and electrochemical techniques. The proton conductivity of the materials depend strongly on hydration, which increases by four orders of magnitude over the relative humidity (RH) range of 20 to 100 %, up to a maximum of 0.027 S cm<jats:sup>–1</jats:sup> at 100  °C and 100 % RH. For the reported samples, proton conduction is believed to occur within a dynamic hydrogen‐bond network formed by functionalized P–OH groups and water molecules by the Grotthuss mechanism. However, the proton conductive sites (P–OH) are likely to be partially immobilized by strong protonic receptors (N atoms in amines), which reduces the free P–OH groups and restricts proton transfer. Hydration may cause a bonding structural rearrangement, which results in more free P–OH groups as active proton conductive sites and, therefore, greatly increased proton conductivity is observed.</jats:p>
Keywords: Hydrolytic stability
Phosphorylated silicas
Proton conduction
Rights: © 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
DOI: 10.1002/adfm.200700350
Published version: http://dx.doi.org/10.1002/adfm.200700350
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