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Ce0.5Zr0.5O2 Powder
Effect of Ba21 Addition on Phase Separation and Oxygen Storage
Capacity of Ce0.5Zr0.5O2 Powder
Chia-Che Chuang, Ming-Jay Chen, Hsing-I Hsiang,w and Fu-Su Yen
Particulate Materials Research Center, Department of Resources Engineering, National Cheng Kung University,
Tainan 70101, Taiwan
Chih-Cheng Chen
Department of Mechanical Engineering, Far East University, Tainan 744, Taiwan
Ce0.5Zr0.5O2 (CZ) plays an important role in three-way catalyst
for its outstanding oxygen storage capacity (OSC). However,
CZ decomposes into Ce- and Zr-rich phases after high-temper-
ature calcinations, which results in the degradation of OSC. In
this study, CZ was synthesized using a coprecipitation method.
Subsequently, different amounts of Ba21 ions were introduced
into the CZ using an incipient wetness impregnation method
followed by calcination at 10001C for 2 h to obtain a series of so-
called BCZa powders. The Ba21 ion addition effects on the
phase development, specific surface area, crystallite size, ag-
glomeration, and OSC of CZ were investigated. The addition of
0.5–3 wt% Ba21 ions significantly increased the specific surface
area and inhibited CZ phase separation. However, with the ad-
dition of Ba21 ions at or above 10 wt%, severe agglomeration
occurred and Ba(CexZr1x)O3 (0oxo1) was detected, both of
which contributed to lowering the OSC of BCZa. With the ad-
dition of 5 wt% Ba21 ions, the BCZa exhibited the maximum
OSC (91.4 lmol/g), due to the high abundance of active oxygen
species on the interface between Ce0.5Zr0.5O2 and BaZrO3.
I. Introduction
CeO2 is an essential component of exhaust-gas treatment sys-
tems in automobiles.1,2 In current three-way catalyst (TWC)
automotive pollution control devices, the reducing and oxidizing
(redox) properties of CeO2 allow the catalyst to enlarge the op-
erating air/fuel ratio window.3,4 In a reducing atmosphere, CeO2
releases oxygen to form CeO2x (where 0.5 x40). However,
in an oxidizing atmosphere, CeO2x easily absorbs oxygen to
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