Electric double layer near electrode and electric field between electrode

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SUMMARY

The discussion centers on the behavior of charged particles in an electrolyte solution when an electric field is applied, specifically referencing the concepts outlined in "Intermolecular and Surface Forces" by Israelachvili. It establishes that the potential drop occurs primarily across the electric double layer at the electrode surfaces, resulting in no electric field within the electrolyte solution itself. Consequently, despite the absence of an electric field in the bulk solution, charged colloidal particles still exhibit movement. The conversation also explores the implications of electron transfer at the electrodes and its effect on the potential drop across the electrolyte.

PREREQUISITES
  • Understanding of electric double layers in electrochemistry
  • Familiarity with the principles of electric fields in electrolyte solutions
  • Knowledge of electron transfer mechanisms at electrodes
  • Basic concepts from "Intermolecular and Surface Forces" by Israelachvili
NEXT STEPS
  • Research the dynamics of electric double layers in electrochemical systems
  • Study the effects of electron transfer on potential distribution in electrolytes
  • Explore the role of electric fields in colloidal particle movement
  • Examine experimental setups for measuring electric fields in electrolyte solutions
USEFUL FOR

Electrochemists, materials scientists, and researchers interested in the behavior of charged particles in electric fields, particularly in the context of electrolyte solutions and electrode interactions.

wonderus
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My question about electrochemistry is best phrase via an exercise in "Intermolecular and surface forces" by Israelachvili (although this is not my homework problem!):

When an electric field is applied across an electrolyte solution containing charged particles they are seen to move parallel or antiparallel to the field depending on the sign of their charge. Now, since almost all of the potential drop must occur across the double layer at each electrode surface, there can be no electric field within the conducting electrolyte solution and hence no force on the charged colloidal particles. Why, then, do the particles move?


When two electrodes applying an electric field across a membrane, is the potential drop across the electrolyte solution the same as that I have applied? I understand that the situation above applies only to charged electrodes without electron transfer. Suppose electron transfer takes place on one or both electrodes, would the potential drop across the electrolyte the same as what I applied? Are there any electric double layers in this case. Thanks.
 
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Can someone tell me what happens if i have two strips(electrodes) of the same metal in an electrolyte. one connected to the -ve end of the battery(Vbias) and the other connected to the positive end.
 
wonderus said:
My question about electrochemistry is best phrase via an exercise in "Intermolecular and surface forces" by Israelachvili (although this is not my homework problem!):

When an electric field is applied across an electrolyte solution containing charged particles they are seen to move parallel or antiparallel to the field depending on the sign of their charge. Now, since almost all of the potential drop must occur across the double layer at each electrode surface, there can be no electric field within the conducting electrolyte solution and hence no force on the charged colloidal particles. Why, then, do the particles move?


When two electrodes applying an electric field across a membrane, is the potential drop across the electrolyte solution the same as that I have applied? I understand that the situation above applies only to charged electrodes without electron transfer. Suppose electron transfer takes place on one or both electrodes, would the potential drop across the electrolyte the same as what I applied? Are there any electric double layers in this case. Thanks.

its is effective only to a certain pint in the solution...the electrostatic force
 

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