All-Solution-Processed Quantum Dot Electrical Double-Layer Transistors Enhanced by Surface Charges of Ti3C2Tx MXene Contacts

ACS Nano ◽  
2021 ◽  
Author(s):  
Hyunho Kim ◽  
Mohamad I. Nugraha ◽  
Xinwei Guan ◽  
Zhenwei Wang ◽  
Mrinal K. Hota ◽  
...  
1978 ◽  
Vol 85 (4) ◽  
pp. 673-683 ◽  
Author(s):  
William B. Russel

A charged particle suspended in an electrolyte solution attracts ions of opposite charge and repels those of like charge. The surface charge and the resulting distributed charge in the fluid comprise an electrical double layer. When a shear flow deforms the diffuse part of the double layer from equilibrium, stresses are generated which make the effective viscosity of the suspension greater than it would be if there were no charges present. In this paper these stresses are calculated for a dilute dispersion of spheres which have small surface charges and which are surrounded by thin double layers. The viscosity is predicted to be Newtonian in extensional flow but shear-thinning with non-zero normal-stress differences in shear flow. For more complex flows a constitutive equation couples the bulk stress directly to the micro-structural deformation responsible for non-Newtonian effects.


2019 ◽  
Author(s):  
Divya Bohra ◽  
Jehanzeb Chaudhry ◽  
Thomas Burdyny ◽  
Evgeny Pidko ◽  
wilson smith

<p>The environment of a CO<sub>2</sub> electroreduction (CO<sub>2</sub>ER) catalyst is intimately coupled with the surface reaction energetics and is therefore a critical aspect of the overall system performance. The immediate reaction environment of the electrocatalyst constitutes the electrical double layer (EDL) which extends a few nanometers into the electrolyte and screens the surface charge density. In this study, we resolve the species concentrations and potential profiles in the EDL of a CO<sub>2</sub>ER system by self-consistently solving the migration, diffusion and reaction phenomena using the generalized modified Poisson-Nernst-Planck (GMPNP) equations which include the effect of volume exclusion due to the solvated size of solution species. We demonstrate that the concentration of solvated cations builds at the outer Helmholtz plane (OHP) with increasing applied potential until the steric limit is reached. The formation of the EDL is expected to have important consequences for the transport of the CO<sub>2</sub> molecule to the catalyst surface. The electric field in the EDL diminishes the pH in the first 5 nm from the OHP, with an accumulation of protons and a concomitant depletion of hydroxide ions. This is a considerable departure from the results obtained using reaction-diffusion models where migration is ignored. Finally, we use the GMPNP model to compare the nature of the EDL for different alkali metal cations to show the effect of solvated size and polarization of water on the resultant electric field. Our results establish the significance of the EDL and electrostatic forces in defining the local reaction environment of CO<sub>2</sub> electrocatalysts.</p>


Membranes ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 129
Author(s):  
Guilherme Volpe Bossa ◽  
Sylvio May

Poisson–Boltzmann theory provides an established framework to calculate properties and free energies of an electric double layer, especially for simple geometries and interfaces that carry continuous charge densities. At sufficiently small length scales, however, the discreteness of the surface charges cannot be neglected. We consider a planar dielectric interface that separates a salt-containing aqueous phase from a medium of low dielectric constant and carries discrete surface charges of fixed density. Within the linear Debye-Hückel limit of Poisson–Boltzmann theory, we calculate the surface potential inside a Wigner–Seitz cell that is produced by all surface charges outside the cell using a Fourier-Bessel series and a Hankel transformation. From the surface potential, we obtain the Debye-Hückel free energy of the electric double layer, which we compare with the corresponding expression in the continuum limit. Differences arise for sufficiently small charge densities, where we show that the dominating interaction is dipolar, arising from the dipoles formed by the surface charges and associated counterions. This interaction propagates through the medium of a low dielectric constant and alters the continuum power of two dependence of the free energy on the surface charge density to a power of 2.5 law.


2021 ◽  
pp. 138416
Author(s):  
Sofia B. Davey ◽  
Amanda P. Cameron ◽  
Kenneth G. Latham ◽  
Scott W. Donne

2021 ◽  
pp. 2000882
Author(s):  
Tong Chen ◽  
Siwei Yang ◽  
Jing Wang ◽  
Wei Chen ◽  
Lifu Liu ◽  
...  

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