Material Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, USA.
J Am Chem Soc. 2013 Feb 13;135(6):2273-8. doi: 10.1021/ja3105889. Epub 2013 Feb 4.
In situ soft X-ray absorption spectroscopy (XAS) was employed to study the adsorption and dissociation of carbon monoxide molecules on cobalt nanoparticles with sizes ranging from 4 to 15 nm. The majority of CO molecules adsorb molecularly on the surface of the nanoparticles, but some undergo dissociative adsorption, leading to oxide species on the surface of the nanoparticles. We found that the tendency of CO to undergo dissociation depends critically on the size of the Co nanoparticles. Indeed, CO molecules dissociate much more efficiently on the larger nanoparticles (15 nm) than on the smaller particles (4 nm). We further observed a strong increase in the dissociation rate of adsorbed CO upon exposure to hydrogen, clearly demonstrating that the CO dissociation on cobalt nanoparticles is assisted by hydrogen. Our results suggest that the ability of cobalt nanoparticles to dissociate hydrogen is the main parameter determining the reactivity of cobalt nanoparticles in Fischer-Tropsch synthesis.
采用原位软 X 射线吸收光谱(XAS)研究了一氧化碳分子在粒径为 4 至 15nm 的钴纳米粒子上的吸附和解离。大多数 CO 分子在纳米粒子表面以分子形式吸附,但有些发生离解吸附,导致纳米粒子表面形成氧化物物种。我们发现 CO 发生离解的趋势与 Co 纳米粒子的尺寸密切相关。事实上,CO 分子在较大的纳米粒子(15nm)上比在较小的粒子(4nm)上更容易发生离解。我们进一步观察到,在暴露于氢气时,吸附 CO 的离解速率明显增加,这清楚地表明,钴纳米粒子上的 CO 离解是由氢气辅助的。我们的结果表明,钴纳米粒子分解氢气的能力是决定其在费托合成中反应性的主要参数。