TY - JOUR
T1 - Formation of Amorphous H3Zr2Si2PO12 by Electrochemical Substitution of Sodium Ions in Na3Zr2Si2PO12 with Protons
AU - Tsukuda, Satoshi
AU - Miyake, Keigo
AU - Yamaguchi, Takuya
AU - Kita, Masao
AU - Ishiyama, Tomohiro
AU - Nishii, Junji
AU - Yamashita, Toshiharu
AU - Kawazoe, Hiroshi
AU - Omata, Takahisa
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid for Scientific Research of Challenging Exploratory Research (Grant No. 15K14126). This work was partly performed under the Cooperative Research Program of the “Network Joint Research Center for Materials and Devices (Nos. 20163006, 20171069 and 20173019)” and “Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials”.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/11/20
Y1 - 2017/11/20
N2 - The sodium ions in Na3Zr2Si2PO12 (NASICON) were substituted with protons using an electrochemical alkali-proton substitution (APS) technique at 400 °C under a 5% H2/95% N2 atmosphere. The sodium ions in NASICON were successfully substituted with protons to a depth of <400 μm from the anode. Completely protonated NASICON, i.e., H3Zr2Si2PO12, was obtained to a depth <40 μm from the anode, although complete protonation of NASICON cannot be achieved by ion exchange in aqueous acid. H3Zr2Si2PO12 was amorphous, whereas the partially protonated NASICON was crystalline, and its unit cell volume decreased with an increase in the extent of substitution. Amorphous H3Zr2Si2PO12 was prepared by pressure-induced amorphization of the NASICON framework, in which an internal pressure of -3.5 GPa was induced by the substitution of large sodium ions with small protons during APS at 400 °C.
AB - The sodium ions in Na3Zr2Si2PO12 (NASICON) were substituted with protons using an electrochemical alkali-proton substitution (APS) technique at 400 °C under a 5% H2/95% N2 atmosphere. The sodium ions in NASICON were successfully substituted with protons to a depth of <400 μm from the anode. Completely protonated NASICON, i.e., H3Zr2Si2PO12, was obtained to a depth <40 μm from the anode, although complete protonation of NASICON cannot be achieved by ion exchange in aqueous acid. H3Zr2Si2PO12 was amorphous, whereas the partially protonated NASICON was crystalline, and its unit cell volume decreased with an increase in the extent of substitution. Amorphous H3Zr2Si2PO12 was prepared by pressure-induced amorphization of the NASICON framework, in which an internal pressure of -3.5 GPa was induced by the substitution of large sodium ions with small protons during APS at 400 °C.
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U2 - 10.1021/acs.inorgchem.7b02060
DO - 10.1021/acs.inorgchem.7b02060
M3 - Article
C2 - 29083885
AN - SCOPUS:85034585914
SN - 0020-1669
VL - 56
SP - 13949
EP - 13954
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 22
ER -