Source: Laboratory of Dr. Yuriy Román — Massachusetts Institute of Technology
A potentiostat/galvanostat (often referred to as simply a potentiostat) is an instrument that measures current at an applied potential (potentiostatic operation) or measures potential at an applied current (galvanostatic operation) (Figure 1). It is the most commonly used instrument in the electrochemical characterization of anode and cathode materials for fuel cells, electrolyzers, batteries, and supercapacitors.
Conventionally, these anode and cathode materials are interfaced with a potentiostat via a three-electrode electrochemical cell. The electrode leads from the potentiostat are connected to the reference electrode, the counter electrode (often called the auxiliary electrode), and the working electrode (which contains the test material of interest). The electrochemical cell is then filled with a high ionic strength electrolyte solution, such as an acidic, alkaline, or salt solution. The media for this high ionic strength solution is typically aqueous; however, for applications necessitating higher operating cell potential windows, such as batteries and supercapacitors, non-aqueous media is often used. The cell media is degassed with an inert gas (to prevent unwanted side reactions) or with a test gas (if the test reaction involves a gas at one of the electrodes).
Alternatively, a salt bridge or membrane is employed to maintain ionic contact if the two half cells are to be measured in different electrolytes. In heterogeneous electrocatalysis, this type of "two compartment" cell is often used if the test molecule at the working electrode is also reactive at the counterelectrode. This happens frequently as the counterelectrode typically employed is platinum, which is a highly active catalyst for many reactions. Here, single compartment cells will be used, where all three electrodes are in the same media.
This video will explain the process of polishing a working electrode, preparing a catalyst ink, mounting the catalyst ink onto the working electrode, preparing the electrochemical cell, and then performing electrochemical measurements. The measurements that are performed include: cyclic voltammetry (CV), linear sweep voltammetry (LSV), chronopotentiometry (CP), and chronoamperometry (CA).
Figure 1. An example of a single compartment electrochemical cell. a.) Teflon cap, b.) glass cell, c.) Pt wire counter electrode, d.) working electrode, e.) Ag/AgCl reference electrode, f.) 0.5 M aqueous sulfuric acid electrolyte solution.
1. Catalyst Ink and Working Electrode Preparation
Safety Precautions: Metals supported on carbon black must be handled in a fume hood or balance enclosure until it is in suspension form as these powders are inhalation hazards.
This procedure will result in figures containing plots of measured current vs. potential for each of the four techniques. By convention for CV and LSV, the plots will also be outputted as measured current vs. potential despite the reality that these are transient techniques that measure current vs. the time derivative of potential.
CV, LSV, CP, and CA are indispensable techniques for determining the efficacy of new electrode materials for fuel cells, electrolyzers, batteries, and supercapacitors as well as for developing fields such as the selective partial oxidation or reduction of commodity chemicals. These methods allow for determining overpotentials of reactions on different electrode materials as compared to their thermodynamic equilibrium potentials. These methods also allow the volumetric or gravimetric capacitance of supercapacitors to be d
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