Gajdardziska-Josifovska Marija, Sharma Renu
Department of Physics and Laboratory for Surface Studies, University of Wisconsin-Milwaukee, Milwaukee, WI 53201, USA.
Microsc Microanal. 2005 Dec;11(6):524-33. doi: 10.1017/S1431927605050403.
Environmental transmission electron microscopy (ETEM) is opening an important window for in situ studies of interaction of water with oxides. Studies of MgO smoke nanocrystals under partial pressures of water ranging from 10 mTorr to 10 Torr found their {100} neutral surfaces to be extremely resistant to dissociative adsorption of water and hydroxylation, in agreement with recent theoretical predictions. ETEM observations of electron irradiation driven MgO smoke nanocrystal hydroxylation displayed the anticipated volume expansion, but revealed complex shape changes with elongations toward oxide corners. The reaction rate was found to increase with electron flux at constant water pressure. In situ selected area diffraction studies of MgO single crystals showed that the hydroxide grows with its basal (0001) plane parallel to the polar MgO (111) planes. This is the same crystallographic relationship as in dehydroxylation experiments, but with four variants. Electron energy loss spectroscopy found oxygen K-edge changes consistent with bulk hydroxylation.
环境透射电子显微镜(ETEM)正在为水与氧化物相互作用的原位研究打开一扇重要的窗口。对氧化镁烟雾纳米晶体在10毫托至10托的水的分压下进行的研究发现,其{100}中性表面对水的解离吸附和羟基化具有极强的抗性,这与最近的理论预测一致。对电子辐照驱动的氧化镁烟雾纳米晶体羟基化的ETEM观察显示出预期的体积膨胀,但揭示了向氧化物角部伸长的复杂形状变化。发现在恒定水压下反应速率随电子通量增加。对氧化镁单晶的原位选区衍射研究表明,氢氧化物以其基面(0001)平行于极性氧化镁(111)面的方式生长。这与脱羟基实验中的晶体学关系相同,但有四种变体。电子能量损失谱发现氧K边的变化与体相羟基化一致。