1980
DOI: 10.1021/ja00534a020
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Photoelectrochemical behavior of n-gallium arsenide electrodes in ambient-temperature molten-salt electrolytes

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Cited by 39 publications
(57 citation statements)
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“…It has been reported that the two anodic waves appeared in dimethyl sulfoxide when acac ¹ was liberated from the iron complex during the reduction process of Fe(acac) 3 . 23 However, only one anodic peak was observed in BMPTFSA, implying that [Fe(acac) 3 6 ] 3¹/4¹ and more negative than those of other iron complexes. It is known that the higher donor property, namely Lewis basicity, of the ligands leads to the stronger interaction between the metal ion and ligand, resulting in the negative shift of the redox potential.…”
Section: Resultsmentioning
confidence: 98%
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“…It has been reported that the two anodic waves appeared in dimethyl sulfoxide when acac ¹ was liberated from the iron complex during the reduction process of Fe(acac) 3 . 23 However, only one anodic peak was observed in BMPTFSA, implying that [Fe(acac) 3 6 ] 3¹/4¹ and more negative than those of other iron complexes. It is known that the higher donor property, namely Lewis basicity, of the ligands leads to the stronger interaction between the metal ion and ligand, resulting in the negative shift of the redox potential.…”
Section: Resultsmentioning
confidence: 98%
“…14,15,22,26 The D value of Fe(acac) 3 in BMPTFSA was much smaller than those in acetonitrile, reflecting the higher viscosity (73 mPa s) of BMPTFSA containing 10 mM Fe(acac) 3 . As abovementioned, the negative redox potentials of [Fe(CN) 6 ] 3¹ and Fe(acac) 3 are considered suitable for the anolyte of the redox flow batteries. The D value of Fe(acac) 3 was larger than that of [Fe(CN) 6 ] 3¹ (0.6 © 10 ¹7 cm 2 s…”
Section: ¹1mentioning
confidence: 99%
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