Afanasiev Pavel, Chouzier Sandra, Czeri Tivadar, Pilet Guillaume, Pichon Christophe, Roy Magalie, Vrinat Michel
Institut de Recherche sur Catalyse et Environnement, Université de Lyon 1, 2 Avenue A. Einstein, 69626 Villeurbanne Cédex, France.
Inorg Chem. 2008 Apr 7;47(7):2303-11. doi: 10.1021/ic7013013. Epub 2008 Mar 5.
Nickel and cobalt hexamethylenetetramine (HMTA) complexes (NO3)2Me(H2O)6(HMTA)2.4H2O were prepared and characterized structurally by single-crystal X-ray diffraction. Both compounds crystallize in the triclinic P1 space group with the same structure. The structures are three-dimensional hydrogen-bonded supramolecular frameworks containing two-dimensional cationic assemblies connected with proton acceptors, which are noncoordinated anionic species (nitrate) and neutral HMTA molecules. Thermal decomposition of these compounds under an inert atmosphere leads to the high-surface-area metal-carbon foams containing nickel and cobalt nanoparticles embedded within onionlike carbon shells. The decomposition process as studied by thermal analysis and in situ X-ray absorption spectroscopy (XAS) measurements occurs as a rapid loss of oxygen in the form of CO, beginning at temperatures as low as 323 K. As the in situ XAS study demonstrated, the evolution of nickel and cobalt coordination spheres occurs with intermediate formation of amorphous metal carbides, which subsequently decompose to the metal nanoparticles covered with carbon shells.
制备了镍和钴的六亚甲基四胺(HMTA)配合物(NO3)2Me(H2O)6(HMTA)2·4H2O,并通过单晶X射线衍射对其进行了结构表征。两种化合物均以相同结构结晶于三斜P1空间群中。其结构为三维氢键超分子框架,包含与质子受体相连的二维阳离子组装体,质子受体为非配位阴离子物种(硝酸盐)和中性HMTA分子。这些化合物在惰性气氛下的热分解会产生高比表面积的金属碳泡沫,其中镍和钴纳米颗粒嵌入洋葱状碳壳内。通过热分析和原位X射线吸收光谱(XAS)测量研究的分解过程,从低至323 K的温度开始,以CO的形式快速失去氧。正如原位XAS研究所表明的,镍和钴配位球的演变伴随着无定形金属碳化物的中间形成,随后分解为覆盖有碳壳的金属纳米颗粒。