1975
DOI: 10.1021/cr60293a002
|View full text |Cite
|
Sign up to set email alerts
|

Proton conduction and injection in solids

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

2
95
1
3

Year Published

1976
1976
2014
2014

Publication Types

Select...
7
3

Relationship

0
10

Authors

Journals

citations
Cited by 277 publications
(103 citation statements)
references
References 57 publications
2
95
1
3
Order By: Relevance
“…When exposed to H 2 gas, Pd absorbs H 2 to form PdH x with x = 0.6 for 0.1 atm < H 2 pressure < 1 atm. 11,21,22 As expected, at V D = 0 V, I D for a solution with a low proton concentration (e.g., pH 11) is larger than I D from a solution with a high proton concentration (e.g., pH 2), and no depletion occurs at pH 0 because µ pH=0 = µ PdH . This is because an increase in proton concentration at the protode surface results in a smaller protochemical potential difference between the loaded PdH x contact and the solution.…”
supporting
confidence: 67%
“…When exposed to H 2 gas, Pd absorbs H 2 to form PdH x with x = 0.6 for 0.1 atm < H 2 pressure < 1 atm. 11,21,22 As expected, at V D = 0 V, I D for a solution with a low proton concentration (e.g., pH 11) is larger than I D from a solution with a high proton concentration (e.g., pH 2), and no depletion occurs at pH 0 because µ pH=0 = µ PdH . This is because an increase in proton concentration at the protode surface results in a smaller protochemical potential difference between the loaded PdH x contact and the solution.…”
supporting
confidence: 67%
“…This type of representation [12] is useful in that it emphasises that, in this condensed type of complex, interaction between the chemically reactive components, X and Y, and the processes of ligand conduction across the complex in the osmotic barrier, require specific proximity of the reactive components, and probably also some specifically articulated conformational movements within the complex. Such conformational mobility is obviously less likely to be required for electron conduction [59-661 and proton conduction [67] than for the conduction of other types of ligand, such as hydrogen atoms carried by ubiquinol [68], or, as may be required in the protonmotive ATPase, 0'-groups carried by the circulation of adenine nucleotides and inorganic phosphate [Eqn (9)] [12]. Returning to the chemiosmotically coupled oxidative and photosynthetic phosphorylation systems represented by Fig.…”
Section: Osmotic Coupling Between Chemiosmotic Reactionsmentioning
confidence: 99%
“…They are still widely used as nonlinear optical devices and the choicest electro -optic materials having wide practical application [2][3][4][5][6][7][8][9][10][11][12][13] . Several researchers have carried out a lot of studies on pure ADP crystals [14][15][16] .…”
Section: Introductionmentioning
confidence: 99%