Reactivity and deconstruction of the (1×2)-Rh(110) surface studied by scanning tunneling microscopy.

The titration of a (2×2)p2mg–O/Rh(110) surface by hydrogen and the subsequent deconstruction of the nonequilibrium (1×2) reconstructed surface has been studied by scanning tunneling microscopy (STM) in a temperature range between 380 and 405 K. The titration reaction is seen to occur via reaction fronts, which start at steps, are elongated in the [11¯0] direction and leave behind a surface covered by diffusing oxygen atoms. Two deconstruction mechanisms are active: A long-range row pairing of adjacent (1×2) rows, which propagates over several hundreds of Å in the [11¯0] direction, and a local hole formation in which Rh atoms detach from the ends of broken [11¯0] rows, diffuse over up to 100 Å and condense into (1×1) islands. Both mechanisms lead to the formation of correlated up–down islands; at step edges, the second one leads to a step retraction. The deconstruction is strongly defect mediated and the STM results indicate that the (1×2) reconstructed surface is most probably metastable. © 2002 American Institute of Physics. [ABSTRACT FROM AUTHOR]