scholarly journals Local Structure and Redox Properties of Amorphous CeO2-TiO2 Prepared Using the H2O2-Modified Sol-Gel Method

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 2148
Author(s):  
Myungju Kim ◽  
Gwanhee Park ◽  
Heesoo Lee

Amorphous CeO2-TiO2 nanoparticles synthesized by the H2O2-modified sol-gel method were investigated in terms of the Ce-O-Ce and Ti-O-Ti linkage, local structure, and redox properties. The decrease in the crystallinity of CeO2-TiO2 by H2O2 addition was confirmed. The metal–oxygen linkage analysis showed the difference in size of the metal–oxygen network between crystalline CeO2-TiO2 and amorphous CeO2-TiO2 due to the O22− formed by H2O2. The local structure of CeO2-TiO2 was analyzed with an extended X-ray absorption fine structure (EXAFS), and the oscillation changes in the k space revealed the disordering of CeO2-TiO2. The decrease in Ce-O bond length and the Ce-O peak broadening was attributed to O22− interfering with the formation of the extended metal–oxygen network. The temperature-programmed reduction of the H2 profile of amorphous CeO2-TiO2 exhibited the disappearance of the bulk oxygen reduction peak and a low-temperature shift of the surface oxygen reduction peak. The H2 consumption increased compared to crystalline CeO2-TiO2, which indicated the improvement of redox properties by amorphization.

2007 ◽  
Vol 18 (5) ◽  
pp. 976-983 ◽  
Author(s):  
Fábio L. Pissetti ◽  
Maria Suzana P. Francisco ◽  
Richard Landers ◽  
Yoshitaka Gushikem

2003 ◽  
Vol 5 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Kyeong Youl Jung ◽  
Seung Bin Park ◽  
Masaya Matsuoka ◽  
Masakazu Anpo

Photoluminescence behavior ofTiO2,SiO2/TiO2binary and Boron-SiO2/TiO2ternary oxides prepared by the sol-gel method was investigated. The differences in their photocatalytic reactivities ofTiO2-based photocatalysts were interpreted in terms of the relationship of the difference in their photoluminescence characteristics. The addition ofSiO2intoTiO2matrix induced new photoluminescence sites, which were due to anchored titanium oxide species (i.e., the formation of Ti–O–Si bonds) located on the surface. The photoluminescence was found to be very sensitive to the presence of oxygen. These new photoluminescence completely disappeared by the addition of boron intoSiO2/TiO2binary oxide, since the emitting sites having a Ti–O–Si bond were destroyed and the new sites having B–O–Ti or Si–O–B bonds were constructed on the surface, being in agreement with the results obtained by FT-IR measurements. For allTiO2-based photocatalysts, a significant quenching of photoluminescence was observed by the addition of oxygen. It was found that the photocatalytic reactivity ofTiO2-based photocatalysts for the decomposition of trichloroethylene was clearly associated with their relative quenching efficiencies of photoluminescence; photocatalyst showing high quenching efficiency exhibited a high photocatalytic reactivity.


1994 ◽  
Vol 177 ◽  
pp. 179-186 ◽  
Author(s):  
Gianni Antonioli ◽  
Pier Paolo Lottici ◽  
Ivano Manzini ◽  
Guglielmina Gnappi ◽  
Angelo Montenero ◽  
...  

2000 ◽  
Vol 262 (1-3) ◽  
pp. 183-190 ◽  
Author(s):  
Jisun Jin ◽  
Shinichi Sakida ◽  
Toshinobu Yoko ◽  
Masayuki Nogami

2013 ◽  
Vol 226 (1-3) ◽  
pp. 747-753 ◽  
Author(s):  
Yusuke Takahashi ◽  
Shiro Kubuki ◽  
Kazuhiko Akiyama ◽  
Katalin Sinkó ◽  
Ernő Kuzmann ◽  
...  

2014 ◽  
Vol 17 (2) ◽  
pp. 055-065 ◽  
Author(s):  
A. Seifitokaldani ◽  
M. Perrier ◽  
O. Savadogo

The electrochemical stability and activity of different compositions of titanium and tantalum oxy-nitride nano-catalysts were investigated for the oxygen reduction reaction (ORR). A new sol-gel method was used to produce a nano-powder mixture of Ti and Ta oxynitride from their alkoxides using urea as a nitrogen source. The precursors prepared by the sol-gel method were annealed in a N2 + 3% H2 atmosphere at determined temperatures (500, 700 and 900 °C) inside a silica tube furnace. X-ray diffraction results proved that by using this method a considerable amount of nitrogen was inserted into the catalyst structure at a relatively low temperature. Energy dispersive spectroscopy showed that the prepared catalyst should be oxidized carbonitride of titanium and/or tantalum. Heat treatment had a major effect on the onset potential by changing the crystallinity of the catalyst, so that the onset potential of titanium oxynitride increased from ca. 0.05 V to 0.65 V vs. NHE by increasing the temperature from 500 to 700 °C. Increasing the Ta concentration also led to a higher onset potential but lower ORR current. For instance, the onset potential for the ORR for tantalum oxynitride heat treated at 700 °C was ca. 0.85 V vs. NHE while this value was ca. 0.65 V vs. NHE for titanium oxynitride. However, the ORR current was 100 times smaller in tantalum oxynitride, most likely because of a low electrochemically active surface area. Electrochemical measurements suggested that an appropriate composition of titanium and tantalum was required to have both a good onset potential and ORR current by improving the catalytic activity and increasing the active surface area and electrical conductivity.


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