TITANS, CEA, IRAMIS, SPEC, CNRS, Université Paris Saclay , CEA Saclay, F-91191 Gif sur Yvette, France.
ACS Nano. 2016 May 24;10(5):5490-8. doi: 10.1021/acsnano.6b01938. Epub 2016 May 12.
The competition between the on-surface synthesis of covalent nanoarchitectures and the self-assembly of star-shaped 1,3,5-Tris(4-iodophenyl)benzene molecules on Au(111) in vacuum is investigated using scanning tunneling microscopy above room temperature. The molecules form covalent polygonal nanoachitectures at the gold surface step edges and at the elbows of the gold reconstruction at low coverage. With coverage increasing two-dimensional halogen-bonded structures appear and grow on the surface terraces. Two different halogen-bonded nanoarchitectures are coexisting on the surface and hybrid covalent-halogen bonded structures are locally observed. At high coverage covalent nanoarchitectures are squeezed at the domain boundary of the halogen-bonded structures. The competitive growth between the covalent and halogen-bonded nanoarchitectures leads to formation of a two-layer film above one monolayer deposition. For this coverage, the covalent nanoarchitectures are propelled on top of the halogen-bonded first layer. These observations open up new opportunities for decoupling covalent nanoarchitectures from catalytically active and metal surfaces in vacuum.
在真空环境中,使用扫描隧道显微镜在室温以上研究了共价纳米结构的表面合成与星形 1,3,5-三(4-碘苯基)苯分子在 Au(111)表面上自组装之间的竞争。在低覆盖率下,分子在金表面台阶边缘和金重构的肘处形成共价多边形纳米结构。随着覆盖率的增加,二维卤键合结构出现在表面台地上并生长。两种不同的卤键合纳米结构在表面上共存,并且局部观察到混合共价-卤键合结构。在高覆盖率下,共价纳米结构在卤键合结构的畴边界处被挤压。共价和卤键合纳米结构之间的竞争生长导致在单层沉积之上形成双层膜。对于这种覆盖率,共价纳米结构被推到卤键合第一层的顶部。这些观察结果为在真空环境中从催化活性和金属表面上解耦共价纳米结构提供了新的机会。