Scanning tunneling microscopy and tunneling spectroscopy studies of niobium-containing H6+xP2W18-xNbxO62 (x=0, 1, 2, 3) Wells-Dawson heteropolyacid catalysts to probe their redox property and oxidation catalysis

被引：0

作者：

Choi, Jung Ho ^{[1
]}

Park, Dong Ryul ^{[1
]}

Park, Sunyoung ^{[1
]}

Song, In Kyu ^{[1
]}

机构：

[1] Seoul Natl Univ, Inst Chem Proc, Sch Chem & Biol Engn, Seoul 151744, South Korea

来源：

KOREAN JOURNAL OF CHEMICAL ENGINEERING | 2011年 / 28卷 / 11期

基金：

新加坡国家研究基金会;

关键词：

Heteropolyacid; Niobium; Scanning Tunneling Microscopy; Negative Differential Resistance; Redox Property; NEGATIVE DIFFERENTIAL RESISTANCE; STM; DEHYDROGENATION; MOLECULES; SURFACE; ARRAYS; FILM;

D O I：

10.1007/s11814-011-0119-0

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Niobium-containing H6+xP2W18-xNxO62 (x=0, 1, 2, 3) Wells-Dawson heteropolyacids (HPAs) were investigated by scanning tunneling microscopy (STM) and tunneling spectroscopy (TS) in order to elucidate their redox properties. The HPAs formed two-dimensional well-ordered monolayer arrays on graphite surface and exhibited a distinctive current-voltage behavior called negative differential resistance (NDR) in their tunneling spectra. NDR peak voltage measured on HPA molecule was correlated with reduction potential and absorption edge energy determined by electrochemical method and UV-visible spectroscopy, respectively. NDR peak voltage of H6+xP2W18-xNxO62 Wells-Dawson HPAs appeared at less negative voltage with increasing reduction potential and with decreasing absorption edge energy. Oxidative dehydrogenation of isobutyraldehyde was also carried out as a model reaction to probe oxidation catalysis of the HPAs. The trend of NDR peak voltage of H6+xP2W18-xNxO62 Wells-Dawson HPAs was well consistent with the trend of yield for methacrolein.

引用

页码：2137 / 2141

页数：5

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