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Room-temperature driven and visible light enhanced dehydrogenation reactions catalysed by basic Au/SrTiO

An Au/SrTiO 3 catalyst with basic properties (Au/SrTiO 3 -urea) was reported for the first time to be efficient for the dehydrogenation of secondary alcohols at room temperature, with iso-propanol (IPA) dehydrogenation as the probe reaction. Different from previous reports that Au/SrTiO 3 was genera...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2016-01, Vol.4 (5), p.1941-1946
Main Authors: Liu, Huimin, Wang, Tao, Zhang, Huabin, Liu, Guigao, Li, Peng, Liu, Lequan, Hao, Dong, Ren, Jian, Chang, Kun, Meng, Xianguang, Wang, Hongmei, Ye, Jinhua
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container_issue 5
container_start_page 1941
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 4
creator Liu, Huimin
Wang, Tao
Zhang, Huabin
Liu, Guigao
Li, Peng
Liu, Lequan
Hao, Dong
Ren, Jian
Chang, Kun
Meng, Xianguang
Wang, Hongmei
Ye, Jinhua
description An Au/SrTiO 3 catalyst with basic properties (Au/SrTiO 3 -urea) was reported for the first time to be efficient for the dehydrogenation of secondary alcohols at room temperature, with iso-propanol (IPA) dehydrogenation as the probe reaction. Different from previous reports that Au/SrTiO 3 was generally regarded as only a photocatalyst in the IPA dehydrogenation reaction, in this work, it was found that Au/SrTiO 3 -urea could also catalyse the reaction at room temperature without light irradiation, with an acetone production rate of 8.2 μmol h −1 (IPA conversion of 41.0%) which was more than 10 times higher than that of Pt/TiO 2 evaluated under the same conditions. Characterization results revealed that the lattice oxygen in SrTiO 3 was involved in the reaction through the Mars-van Krevelen mechanism, while Au facilitated the cleavage of C-H bonds of the adsorbed reactant with the assistance of a base. Its catalytic activity was further increased to 16.5 μmol h −1 (IPA conversion of 82.5%) after the introduction of visible light. It is regarded that the photon induced photocatalytic performance was significantly enhanced with the existence of instantaneously generated oxygen vacancies. Additionally, the conversion of IPA (82.5%) and the rate of acetone production over Au/SrTiO 3 -urea (16.5 μmol h −1 ) after visible light irradiation for 1 h were 12.3 times and 2.5 times as high as those over Au/P25 (IPA conversion of 6.7% and acetone production rate of 6.7 μmol h −1 ), a catalyst which was also reported to be active in IPA dehydrogenation without light irradiation. This study provides a method for designing efficient catalysts for the dehydrogenation of secondary alcohols at room temperature. An Au/SrTiO 3 catalyst with basic properties (Au/SrTiO 3 -urea) was firstly reported to be efficient for the dehydrogenation of secondary alcohols at room temperature.
doi_str_mv 10.1039/c5ta09174h
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Different from previous reports that Au/SrTiO 3 was generally regarded as only a photocatalyst in the IPA dehydrogenation reaction, in this work, it was found that Au/SrTiO 3 -urea could also catalyse the reaction at room temperature without light irradiation, with an acetone production rate of 8.2 μmol h −1 (IPA conversion of 41.0%) which was more than 10 times higher than that of Pt/TiO 2 evaluated under the same conditions. Characterization results revealed that the lattice oxygen in SrTiO 3 was involved in the reaction through the Mars-van Krevelen mechanism, while Au facilitated the cleavage of C-H bonds of the adsorbed reactant with the assistance of a base. Its catalytic activity was further increased to 16.5 μmol h −1 (IPA conversion of 82.5%) after the introduction of visible light. It is regarded that the photon induced photocatalytic performance was significantly enhanced with the existence of instantaneously generated oxygen vacancies. 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Its catalytic activity was further increased to 16.5 μmol h −1 (IPA conversion of 82.5%) after the introduction of visible light. It is regarded that the photon induced photocatalytic performance was significantly enhanced with the existence of instantaneously generated oxygen vacancies. Additionally, the conversion of IPA (82.5%) and the rate of acetone production over Au/SrTiO 3 -urea (16.5 μmol h −1 ) after visible light irradiation for 1 h were 12.3 times and 2.5 times as high as those over Au/P25 (IPA conversion of 6.7% and acetone production rate of 6.7 μmol h −1 ), a catalyst which was also reported to be active in IPA dehydrogenation without light irradiation. This study provides a method for designing efficient catalysts for the dehydrogenation of secondary alcohols at room temperature. 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A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Huimin</au><au>Wang, Tao</au><au>Zhang, Huabin</au><au>Liu, Guigao</au><au>Li, Peng</au><au>Liu, Lequan</au><au>Hao, Dong</au><au>Ren, Jian</au><au>Chang, Kun</au><au>Meng, Xianguang</au><au>Wang, Hongmei</au><au>Ye, Jinhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Room-temperature driven and visible light enhanced dehydrogenation reactions catalysed by basic Au/SrTiO</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2016-01-26</date><risdate>2016</risdate><volume>4</volume><issue>5</issue><spage>1941</spage><epage>1946</epage><pages>1941-1946</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>An Au/SrTiO 3 catalyst with basic properties (Au/SrTiO 3 -urea) was reported for the first time to be efficient for the dehydrogenation of secondary alcohols at room temperature, with iso-propanol (IPA) dehydrogenation as the probe reaction. Different from previous reports that Au/SrTiO 3 was generally regarded as only a photocatalyst in the IPA dehydrogenation reaction, in this work, it was found that Au/SrTiO 3 -urea could also catalyse the reaction at room temperature without light irradiation, with an acetone production rate of 8.2 μmol h −1 (IPA conversion of 41.0%) which was more than 10 times higher than that of Pt/TiO 2 evaluated under the same conditions. Characterization results revealed that the lattice oxygen in SrTiO 3 was involved in the reaction through the Mars-van Krevelen mechanism, while Au facilitated the cleavage of C-H bonds of the adsorbed reactant with the assistance of a base. Its catalytic activity was further increased to 16.5 μmol h −1 (IPA conversion of 82.5%) after the introduction of visible light. It is regarded that the photon induced photocatalytic performance was significantly enhanced with the existence of instantaneously generated oxygen vacancies. Additionally, the conversion of IPA (82.5%) and the rate of acetone production over Au/SrTiO 3 -urea (16.5 μmol h −1 ) after visible light irradiation for 1 h were 12.3 times and 2.5 times as high as those over Au/P25 (IPA conversion of 6.7% and acetone production rate of 6.7 μmol h −1 ), a catalyst which was also reported to be active in IPA dehydrogenation without light irradiation. This study provides a method for designing efficient catalysts for the dehydrogenation of secondary alcohols at room temperature. An Au/SrTiO 3 catalyst with basic properties (Au/SrTiO 3 -urea) was firstly reported to be efficient for the dehydrogenation of secondary alcohols at room temperature.</abstract><doi>10.1039/c5ta09174h</doi><tpages>6</tpages></addata></record>
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title Room-temperature driven and visible light enhanced dehydrogenation reactions catalysed by basic Au/SrTiO
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