The interaction between Pt and its various supports can regulate the intrinsic electronic structure of Pt particles and their catalytic performance.Herein,Pt/CeO2 and Pt/SiC catalysts were successfully prepared via a ...The interaction between Pt and its various supports can regulate the intrinsic electronic structure of Pt particles and their catalytic performance.Herein,Pt/CeO2 and Pt/SiC catalysts were successfully prepared via a facile Pt colloidal particle deposition method,and their catalytic performance in CO oxidation was investigated.XRD,TEM,XPS and H2-TPR were used to identify the states of Pt particles on the support surface,as well as their effect on the performance of the catalysts.Formation of the Pt-O-Ce interaction is one of the factors controlling catalyst activity.Under the oxidative treatment at low temperature,the Pt-O-Ce interaction plays an important role in improving the catalytic activity.After calcining at high temperature,enhanced Pt-O-Ce interaction results in the absence of metallic Pt0 on the support surface,as evidenced by the appearance of Pt2+species.It is consistent with the XPS data of Pt/CeO2,and is the main reason behind the deactivation of the catalyst.By contrast,either no interaction is formed between Pt and SiC or Pt nanoparticles remain in the metallic Pt0 state on the SiC surface even after aging at 800℃in an oxidizing atmosphere.Thus,the Pt/SiC shows better thermal stability than Pt/CeO2.The interaction between Pt and the active support may be concluded to be essential for CO oxidation at low temperature,but strong interactions may induce serious deactivation of catalytic activity.展开更多
In this paper the hydrogen and hydrocarbon gas sensing performance of the Pt/Catalysed TiO_2/SiC devices have been studied.The TiO_2 metal oxide thin films were catalytically modified employing Pt and Pd.The electrica...In this paper the hydrogen and hydrocarbon gas sensing performance of the Pt/Catalysed TiO_2/SiC devices have been studied.The TiO_2 metal oxide thin films were catalytically modified employing Pt and Pd.The electrical properties of the fabricated devices were studied by measuring their capacitance-voltage (C-V),conductance-voltage (G-V) and dynamic response characteristics.The sensor's response as a function of operating temperature (25℃to 700℃) and concentrations less than 1% of the analyte gases have been investigated.The sensitivity of the Pt catalysed TiO_2 sensor was found to be superior when compared to TiO_2 catalysed with Pd.A voltage shift of 3.2 V for 1% propene at 420℃and 2.8 V for 1% hydrogen at 250℃in an ambient containing synthetic air was recorded for the Pt catalysed TiO_2 sensor.The response of Pt catalysed TiO_2 sensor was found to be approximately 4 times larger when compared to the non catalysed counterpart.展开更多
基金Project supported by the National Natural Science Foundation of China(21506194,21676255)the Natural Science Foundation of Zhejiang Province,China(Y16B070025).
文摘The interaction between Pt and its various supports can regulate the intrinsic electronic structure of Pt particles and their catalytic performance.Herein,Pt/CeO2 and Pt/SiC catalysts were successfully prepared via a facile Pt colloidal particle deposition method,and their catalytic performance in CO oxidation was investigated.XRD,TEM,XPS and H2-TPR were used to identify the states of Pt particles on the support surface,as well as their effect on the performance of the catalysts.Formation of the Pt-O-Ce interaction is one of the factors controlling catalyst activity.Under the oxidative treatment at low temperature,the Pt-O-Ce interaction plays an important role in improving the catalytic activity.After calcining at high temperature,enhanced Pt-O-Ce interaction results in the absence of metallic Pt0 on the support surface,as evidenced by the appearance of Pt2+species.It is consistent with the XPS data of Pt/CeO2,and is the main reason behind the deactivation of the catalyst.By contrast,either no interaction is formed between Pt and SiC or Pt nanoparticles remain in the metallic Pt0 state on the SiC surface even after aging at 800℃in an oxidizing atmosphere.Thus,the Pt/SiC shows better thermal stability than Pt/CeO2.The interaction between Pt and the active support may be concluded to be essential for CO oxidation at low temperature,but strong interactions may induce serious deactivation of catalytic activity.
文摘In this paper the hydrogen and hydrocarbon gas sensing performance of the Pt/Catalysed TiO_2/SiC devices have been studied.The TiO_2 metal oxide thin films were catalytically modified employing Pt and Pd.The electrical properties of the fabricated devices were studied by measuring their capacitance-voltage (C-V),conductance-voltage (G-V) and dynamic response characteristics.The sensor's response as a function of operating temperature (25℃to 700℃) and concentrations less than 1% of the analyte gases have been investigated.The sensitivity of the Pt catalysed TiO_2 sensor was found to be superior when compared to TiO_2 catalysed with Pd.A voltage shift of 3.2 V for 1% propene at 420℃and 2.8 V for 1% hydrogen at 250℃in an ambient containing synthetic air was recorded for the Pt catalysed TiO_2 sensor.The response of Pt catalysed TiO_2 sensor was found to be approximately 4 times larger when compared to the non catalysed counterpart.
