PROBING THE OXIDATIVE ETCHING KINETICS OF METALS WITH THE FEEDBACK MODE OF THE SCANNING ELECTROCHEMICAL MICROSCOPE

Citation
Jv. Macpherson et al., PROBING THE OXIDATIVE ETCHING KINETICS OF METALS WITH THE FEEDBACK MODE OF THE SCANNING ELECTROCHEMICAL MICROSCOPE, Journal of the Chemical Society. Faraday transactions, 92(20), 1996, pp. 3799-3805
Citations number
39
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
ISSN journal
09565000
Volume
92
Issue
20
Year of publication
1996
Pages
3799 - 3805
Database
ISI
SICI code
0956-5000(1996)92:20<3799:PTOEKO>2.0.ZU;2-Y
Abstract
The conditions under which the feedback mode of the scanning electroch emical microscope (SECM) can be used to probe the oxidative etching ki netics of metals most effectively are considered. In this application, the oxidant of interest is electrogenerated at the tip ultramicroelec trode (UME) of an SECM from a solution containing only the reduced for m of the redox couple. In this study, tris (2,2'-bipyridyl)ruthenium(I II) [Ru(bipy)(3)(3+)] is generated in aqueous potassium nitrate soluti ons through the oxidation of Ru(bipy)(3)(2+), and bromine is formed th rough the oxidation of bromide in aqueous sulfuric acid solutions. The oxidant diffuses to an unbiased metal substrate, where it may induce oxidative etching, resulting in the anodic dissolution of the metal. I n the process, the mediator is converted back to its reduced form and fed back to the tip by diffusion, thereby enhancing the current. When the substrate is effectively infinite in size compared to the tip UME, its potential is fixed by the bulk solution conditions at a value tha t also promotes diffusion-controlled positive feedback of the mediator . Thus, feedback current measurements under these conditions may not s imply reflect the kinetics of etching. SECM imaging experiments with P t substrate electrodes, which are inert with respect to anodic dissolu tion with the two oxidants of interest, demonstrate that this complica tion can be circumvented by decreasing the size of the substrate elect rode to the dimensions of the tip UME. Under these conditions, substra te potential-driven feedback at an unbiased metal becomes negligible, allowing etching kinetics to be studied in isolation. Investigations o f Cu etching with both Ru(bipy)(3)(3+) and Br-2, under these condition s reveal, unambiguously, that the metal dissolution process is diffusi on-controlled under all of the conditions examined, suggesting that th e heterogeneous rate constant controlling the etching process is large . In the case of the reaction with Ru(bipy)(3)(3+), a minimum rate con stant of 0.4 cm s(-1) is estimated for the interfacial reaction, assum ing a first-order process. On a general level, the studies provide new information on the imaging capabilities of SECM in the feedback mode with unbiased substrates.