2022
DOI: 10.1016/j.electacta.2022.139923
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Effect of nanoparticle size on the near-surface pH-distribution in aqueous and carbonate buffered solutions

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Cited by 10 publications
(5 citation statements)
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“…3a), Cu was predicted to be entirely or primarily solid (CuO at pe 5 and Cu 2 O at pe 3.4). When the pH decreased to pH 6.5 and 5, as expected for the surface pH of the electrode during anodic polarization, 41 the relative concentration of aqueous Cu-chloride species increased. There were no solid species predicted at pH 5.…”
Section: Resultsmentioning
confidence: 58%
See 1 more Smart Citation
“…3a), Cu was predicted to be entirely or primarily solid (CuO at pe 5 and Cu 2 O at pe 3.4). When the pH decreased to pH 6.5 and 5, as expected for the surface pH of the electrode during anodic polarization, 41 the relative concentration of aqueous Cu-chloride species increased. There were no solid species predicted at pH 5.…”
Section: Resultsmentioning
confidence: 58%
“…Other input values were 1 mM of the respective amino acid, 9 g l −1 NaCl, pH values of 5, 6.5 and 7.4, a temperature of 25 °C, and a pressure of 1 atm. The lower pH values simulate oxidative conditions present under anodic polarization, 41 and the temperature was chosen to benefit from the best availability of literature data. Solids were allowed to form and precipitate.…”
Section: Methodsmentioning
confidence: 99%
“… where the index i denotes the chemical species (H + , OH − and the buffer ions), c the concentration, D the diffusion coefficient, r the radial distance from the centre, z the electric charge, e 0 Coulomb’s constant, k B Boltzmann’s constant and ϕ the electrical potential. Due to the short diffusion pathways of only a few µm, the set of partial differential equations can be solved for steady-state conditions, as further described in [ 23 ] for the case of flat surfaces and NP geometries [ 24 ]. Given the high I c of the solution, the gradient of the electric potential is small, and the migration term in Equation (1) can be simplified to the case of diffusion only.…”
Section: Methodsmentioning
confidence: 99%
“…This, in turn, affects cellular interactions, transport mechanisms, accumulation and/or excretion of the therapeutic potential of NPs [ 21 , 22 ]. In addition, local pH shifts caused by chemical reactions on the particle surface must be considered, as these might have a strong impact on the local environment [ 23 ] due to stronger pH gradients around smaller NPs [ 24 ]. However, steep pH gradients between the dispersant and the particle surface would further acidify the NP environment, which could be exploited in wound healing.…”
Section: Introductionmentioning
confidence: 99%
“…Some of the authors of this study have shown in simulations that the pH-gradients are steeper (and closer to the NP surface) for smaller nanoparticles. 23 These differences to planar surfaces become significant for nanoparticle sizes <10 nm. Second, time-of-flight secondary ion mass spectrometry measurements performed on the 5 and 50 nm Au NPs of this study showed a strong interaction between the 5 nm Au NPs and cysteine, 9 forming an Au thiolate complex.…”
Section: Cyclic Voltammetry Of Differently Sized Au Nps Immobilized Onmentioning
confidence: 99%