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Role of B5-Type Sites in Ru Catalysts used for the NH3 Decomposition Reaction

机译:B5型位点在用于NH3分解反应的Ru催化剂中的作用

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A series of activated carbon supported Ru catalysts have been reduced at different temperatures under hydrogen flow, and in some cases under ammonia flow, in order to modify the morphology and the particle size of the metallic active sites. CO chemisorption and transmission electron microscopy have been applied to follow the variations of these particles. The samples have been tested in the ammonia decomposition reaction, where systematic differences in catalytic activities as consequence of the support modification as well as due to the changes in the Ru particle sizes have been detected. Furthermore when potassium is added as catalyst promoter the sintering of Ru particles is significantly diminished and thus the changes in catalytic activities are inhibited. The electronic states of the Ru particles have been evaluated by determination of the chemisorption heats of the CO probe molecule. A part of other promoter or support effects it seems to exit a critical mean size for Ru particles on where maximum of catalytic activity is achieved. This behavior can be rationalized by the presence of surface highly active B5 sites, which consist of an arrangement of three Ru atoms in one layer and two further Ru atoms in an internal layer. These especial surface sites are expected to be in a higher proportion over Ru crystallites of those critical sizes, namely for Ru diameter sizes in the rage of 3-5 nm.
机译:为了改变金属活性部位的形态和粒径,在氢气流下,在某些情况下在氨流下,在不同温度下还原了一系列活性炭负载的Ru催化剂。一氧化碳化学吸收和透射电子显微镜已被应用于跟踪这些粒子的变化。已在氨分解反应中对样品进行了测试,其中已检测到由于载体改性以及Ru粒径变化导致的催化活性的系统差异。此外,当添加钾作为催化剂促进剂时,Ru颗粒的烧结显着减少,因此抑制了催化活性的变化。通过确定CO探针分子的化学吸附热来评估Ru颗粒的电子态。其他促进剂或支持作用的一部分似乎在达到最大催化活性的位置上超出了Ru颗粒的临界平均尺寸。可以通过存在表面高活性的B5位来使这种行为合理化,该位点由一层中的三个Ru原子和内层中的另外两个Ru原子组成。预期这些特殊的表面位置将比那些临界尺寸的Ru微晶比例更高,即Ru直径尺寸在3-5 nm之间。

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