Soy Esin, Guisinger Nathan P, Trenary Michael
Department of Chemistry, University of Illinois at Chicago , 845 West Taylor Street, Chicago, Illinois 60607, United States.
Center for Nanoscale Materials, Argonne National Laboratory , Argonne, Illinois 60439, United States.
J Phys Chem B. 2018 Jan 18;122(2):572-577. doi: 10.1021/acs.jpcb.7b05064. Epub 2017 Jul 18.
We report scanning tunneling microscopy results on the nucleation and growth of Pd nanoclusters on a single layer of graphene on the Cu(111) surface. The shape, organization, and structural evolution of the Pd nanoclusters were investigated using two different growth methods, continuous and stepwise. The size and shape of the formed nanoclusters were found to greatly depend on the growth technique used. The size and density of spherical Pd nanoclusters increased with increasing coverage during stepwise deposition as a result of coarsening of existing clusters and continued nucleation of new clusters. In contrast, continuous deposition gave rise to well-defined triangular Pd clusters as a result of anisotropic growth on the graphene surface. Exposure to ethylene caused a decrease in the size of the Pd clusters. This is attributed to the exothermic formation of ethylidyne on the cluster surfaces and an accompanying weakening of the Pd-Pd bonding.
我们报告了在Cu(111)表面单层石墨烯上钯纳米团簇成核与生长的扫描隧道显微镜结果。使用连续和分步两种不同的生长方法研究了钯纳米团簇的形状、组织和结构演变。发现所形成的纳米团簇的尺寸和形状很大程度上取决于所使用的生长技术。在分步沉积过程中,由于现有团簇的粗化和新团簇的持续成核,球形钯纳米团簇的尺寸和密度随着覆盖率的增加而增大。相比之下,由于在石墨烯表面的各向异性生长,连续沉积产生了形状规则的三角形钯团簇。暴露于乙烯会导致钯团簇尺寸减小。这归因于在团簇表面放热形成次乙基以及伴随的钯-钯键的减弱。