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Electron transfer to iron(III) oxide colloids

Conference ·
OSTI ID:5570873
The electron transfer reaction from viologen radicals to colloidal iron(III) oxide and oxyhydroxide particles was investigated by pulse and steady-state radiolysis techniques. The rate of electron injection to oxyhydroxide particles was clearly controlled by their surface charge and in the region near the isoelectric point, the electron transfer rate is slower than the diffusion-controlled rate by at least two orders of magnitude. Conductivity measurements clearly reveal the occurrence of protonation reactions immediately following the initial electron transfer step. On the basis of the experimentally measured ratio of protons consumed to electrons injected, a mechanistic pathway describing the sequence of protonation reactions is proposed. The competition between surface trapping of charge and the migration of charge into the interior of the particles and the factors controlling these two events are also discussed. 17 refs., 3 figs.
Research Organization:
Melbourne Univ., Parkville (Australia). Dept. of Physical Chemistry; Argonne National Lab., IL (USA)
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
5570873
Report Number(s):
CONF-8710229-1; ON: DE88002885
Country of Publication:
United States
Language:
English

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