Department of Energy Systems Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST) , Daegu 711-817, Korea.
ACS Appl Mater Interfaces. 2013 Nov 27;5(22):12197-204. doi: 10.1021/am4043245. Epub 2013 Nov 12.
The deposition of polyoxometalate (POM) on chemically reduced graphene oxide sheets was carried out through electron transfer interaction and electrostatic interaction between POM and graphene sheets to make a heterogeneous catalyst in aqueous media. Well dispersed individual phosphomolybdic acid (PMo) clusters were observed by electron microscopy and atomic force microscopy measurements. The interaction between polyoxometalate and the graphene sheet was confirmed by using various spectroscopic methods such as FT-IR, UV-vis, and Raman. The UV-visible, IR, and cyclic voltammetry results revealed alteration of the electronic structure of deposited PMo as a result of strong interaction with the graphene oxide surface. Electrochemical properties of the PMo-rGO catalyst were investigated in an aqueous acidic electrolyte. The hybrid catalyst showed enhanced electro-oxidation of nitrite compared with pure homogeneous PMo and rGO.
通过多酸(POM)与石墨烯片之间的电子转移相互作用和静电相互作用,将多酸沉积在化学还原的氧化石墨烯片上,在水介质中制得非均相催化剂。电子显微镜和原子力显微镜测量表明,观察到了分散良好的单个磷钼酸(PMo)簇。通过各种光谱方法,如傅里叶变换红外(FT-IR)、紫外可见(UV-vis)和拉曼(Raman),证实了多酸与石墨烯片之间的相互作用。紫外可见、红外和循环伏安法的结果表明,由于与氧化石墨烯表面的强相互作用,沉积的 PMo 的电子结构发生了改变。在酸性水溶液电解质中研究了 PMo-rGO 催化剂的电化学性质。与纯均相 PMo 和 rGO 相比,该杂化催化剂显示出增强的亚硝酸盐电氧化性能。