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Spectroscopic determination of flatband potentials for polycrystalline TiO[sub 2] electrodes in nonaqueous solvents

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100109a029· OSTI ID:6296744
;  [1]
  1. University College, Dublin (Ireland)

The flatband potential V[sub fb] of a polycrystalline TiO[sub 2] electrode has been determined, using a newly developed spectroscopic technique, in a range of nonaqueous solvents (MeCN, THF, DMF, MeOH, and EtOH). It has been found that V[sub fb] is significantly more positive for water and nonaqueous protic solvents (MeOH and EtOH) than for nonaqueous aprotic solvents (MeCN, DMF, and THF) due to establishment of a proton adsorption-desorption equilibrium. Further, the authors observe that V[sub fb] is independent of the electrolyte used in nonaqueous protic solvents, but in nonaqueous aprotic solvents V[sub fb] may depend on the electrolyte cation. Cations which have been found to be potential determining are Li[sup +], Na[sup +], and Mg[sup +]. Results indicating that both cation adsorption and intercalation are important in determining V[sub fb] are presented. 23 refs., 4 figs., 4 tabs.

OSTI ID:
6296744
Journal Information:
Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 97:7; ISSN JPCHAX; ISSN 0022-3654
Country of Publication:
United States
Language:
English