Alayoglu Selim, Rosenberg Daniel J, Ahmed Musahid
Chemical Sciences Division, Lawrence Berkeley National Laboratory, USA.
Dalton Trans. 2016 Jun 14;45(24):9932-41. doi: 10.1039/c6dt00204h.
A nano-catalyst comprised of oxidized Co NPs supported on MgO nano-plates was synthesized via a hydrothermal co-precipitation strategy and calcination in O2 and subsequently in H2 at 250 °C. Spectro-microscopy characterization was performed by scanning transmission electron microscopy, electron energy loss spectroscopy and scanning X-ray transmission microscopy. Surface measurements under H2 and H2 + CO atmospheres were obtained by ambient pressure X-ray photoelectron spectroscopy and in situ X-ray absorption spectroscopy in the 225-480 °C range. These measurements at the atomic and microscopic levels demonstrated that the oxidized Co nanoparticles uniformly decorated the MgO nano-plates. The surfaces are enriched with Co, and with a mixture of Co(OH)2 and CoO under H2 and H2 + CO atmospheres. Under a H2 atmosphere, the outermost surfaces were composed of (lattice) O(2-), CO3(2-) and OH(-). No inorganic carbonates were observed in the bulk. Chemisorbed CO, likely on the oxidized Co surfaces, was observed at the expense of O(2-) under 300 mTorr H2 + CO (2 : 1) at 225 °C. Gas phase CO2 was detected under 32 Torr H2 + CO (2 : 1) at 225 °C upon prolonged reaction time, and was attributed to a surface chemical reaction between O(2-) and chemisorbed CO. Furthermore, sp(3) like carbon species were detected on the otherwise carbon free surface in H2 + CO, which remained on the surface under the subsequent reaction conditions. The formation of sp(3) like hydrocarbons was ascribed to a surface catalytic reaction between the chemisorbed CO and OH(-) as the apparent hydrogen source.
通过水热共沉淀策略以及在氧气中随后在250℃氢气中进行煅烧,合成了一种由负载在氧化镁纳米片上的氧化钴纳米颗粒组成的纳米催化剂。通过扫描透射电子显微镜、电子能量损失谱和扫描X射线透射显微镜进行光谱显微镜表征。在225-480℃范围内,通过常压X射线光电子能谱和原位X射线吸收光谱获得了氢气和氢气+一氧化碳气氛下的表面测量结果。这些在原子和微观水平上的测量表明,氧化钴纳米颗粒均匀地修饰在氧化镁纳米片上。在氢气和氢气+一氧化碳气氛下,表面富含钴,并含有氢氧化钴和氧化钴的混合物。在氢气气氛下,最外层表面由(晶格)O(2-)、CO3(2-)和OH(-)组成。在本体中未观察到无机碳酸盐。在225℃、300 mTorr氢气+一氧化碳(2∶1)条件下,观察到化学吸附的一氧化碳,可能吸附在氧化钴表面,以O(2-)为代价。在225℃、32 Torr氢气+一氧化碳(2∶1)条件下,长时间反应后检测到气相二氧化碳,这归因于O(2-)与化学吸附的一氧化碳之间的表面化学反应。此外,在氢气+一氧化碳气氛下,在原本无碳的表面上检测到类sp(3)碳物种,在随后的反应条件下这些物种保留在表面上。类sp(3)碳氢化合物的形成归因于化学吸附的一氧化碳与作为明显氢源的OH(-)之间的表面催化反应。