TY - JOUR
T1 - Mechanistic Insights into Hydration of Solid Oxides
AU - Jing, Yuhang
AU - Matsumoto, Hiroshige
AU - Aluru, Narayana R.
N1 - Funding Information:
This work was supported by the National Science Foundation (USA) under Grant No. 1545907, the NSF of China under Grant No. 11304059 the NSF of Heilongjiang Province of China under Grant No. QC2015001 and the International Postdoctoral Exchange Fellowship Program of China under Grant No. 20140016.
Funding Information:
This work was supported by the National Science Foundation (USA) under Grant No. 1545907, the NSF of China under Grant No. 11304059, the NSF of Heilongjiang Province of China under Grant No. QC2015001, and the International Postdoctoral Exchange Fellowship Program of China under Grant No. 20140016. This research is part of the Blue Waters sustained-petascale computing project, which is supported by the National Science Foundation (awards OCI-0725070 and ACI-1238993) and the state of Illinois. Blue Waters is a joint effort of the University of Illinois at Urbana−Champaign and its National Center for Supercomputing Applications (NCSA). We acknowledge the financial support of NCSA for Dr. Yuhang Jing’s Postdoctoral Research Associate. We thank Tao Sun and Linjian Ma for helpful discussions.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2018/1/9
Y1 - 2018/1/9
N2 - Some of the solid oxide materials, used in solid oxide fuel and electrolysis cells, are known to conduct protons once they are hydrated. However, the mechanisms by which solid oxide materials get hydrated is not clear. By performing detailed density functional theory calculations, we investigate hydration of two typical solid oxides with a single-crystal structure - a proton-conducting yttrium-doped strontium zirconate (SZY) and an oxide ion-conducting yttria-stabilized zirconia (YSZ). We suggest a four-step process to understand the hydration of solid oxides - water adsorption on the surface, proton migration from the surface to bulk, proton migration in the bulk, and oxide ion vacancy migration in the bulk. The hydroxide ion migration with a lower energy barrier, compared to the proton hopping mechanism, is proposed for the conduction of proton between the surface and subsurface of the perovskite oxide. Our analysis provides mechanistic insights into the hydration of single-crystal SZY and nonhydration of single-crystal YSZ. The study presented here not only explains the hydration of materials but also provides the importance of structural rearrangement when a proton is incorporated into the bulk of the solid oxide material.
AB - Some of the solid oxide materials, used in solid oxide fuel and electrolysis cells, are known to conduct protons once they are hydrated. However, the mechanisms by which solid oxide materials get hydrated is not clear. By performing detailed density functional theory calculations, we investigate hydration of two typical solid oxides with a single-crystal structure - a proton-conducting yttrium-doped strontium zirconate (SZY) and an oxide ion-conducting yttria-stabilized zirconia (YSZ). We suggest a four-step process to understand the hydration of solid oxides - water adsorption on the surface, proton migration from the surface to bulk, proton migration in the bulk, and oxide ion vacancy migration in the bulk. The hydroxide ion migration with a lower energy barrier, compared to the proton hopping mechanism, is proposed for the conduction of proton between the surface and subsurface of the perovskite oxide. Our analysis provides mechanistic insights into the hydration of single-crystal SZY and nonhydration of single-crystal YSZ. The study presented here not only explains the hydration of materials but also provides the importance of structural rearrangement when a proton is incorporated into the bulk of the solid oxide material.
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U2 - 10.1021/acs.chemmater.7b03476
DO - 10.1021/acs.chemmater.7b03476
M3 - Article
AN - SCOPUS:85040313037
VL - 30
SP - 138
EP - 144
JO - Chemistry of Materials
JF - Chemistry of Materials
SN - 0897-4756
IS - 1
ER -