Name: pulse voltage methods for electrochemistry
Uploaded: 2024-12-05T18:31:57.000Z
Duration: 1 min 17 s
Channel: JoVE

Ograniczenia woltamperometrii liniowo-skanującej są pokonywane za pomocą metod impulsowych, takich jak woltamperometria różnicowa i woltamperometria prostokątna, które mierzą prąd faradowy bez zakłócającego prądu ładowania.
Woltamperometria różnicowo-impulsowa wykorzystuje sekwencję impulsów potencjału nałożonych na liniową rampę potencjału. Na każdym kroku przez krótki czas przykładany jest impuls o wyższym potencjale, a prąd jest mierzony tuż przed i na końcu impulsu.
Różnica prądu jest wykreślana w stosunku do przyłożonego potencjału do wygenerowania woltammogogramu. Maksimum tego prądu jest proporcjonalne do stężenia analitu w roztworze.
Woltamperometria falowa prostokątna wykorzystuje kształt fali, który łączy falę prostokątną i schody. W tym procesie analit jest redukowany na powierzchni elektrody podczas impulsów katodowych i ponownie utleniany podczas impulsów anodowych.
Polarogram fali prostokątnej mierzy różnicę prądu między dwoma punktami.
Ponieważ oba prądy mają przeciwstawne znaki, prąd wynikowy oszacowany na podstawie ich różnicy jest większy i jest wprost proporcjonalny do stężenia analitu.

techniki woltamperometrii: woltamperometria impulsowa

Voltammetric Techniques: Pulse Voltammetry

Woltamperometria różnicowo-impulsowa (DPV) to rodzaj woltamperometrii, który polega na przyłożeniu serii impulsów napięcia do ogniwa elektrochemicznego podczas pomiaru powstałego prądu. W DPV impuls różnicowy lub małe impulsy potencjału są nakładane na liniowy przebieg potencjału. Wielkość tych impulsów jest zazwyczaj niewielka, często w zakresie miliwoltów. Każdy impuls napięcia trwa krótko, zwykle rzędu kilku milisekund, i jest przyłożony w regularnych odstępach czasu wzdłuż przebiegu potencjału.

 Podstawowa zasada DPV polega na tym, że przyłożenie impulsu potencjału do układu elektrochemicznego generuje prąd faradajowski, który powstaje w wyniku reakcji redoks zachodzących na powierzchni elektrody. Ten prąd faradajowski powstaje w wyniku transferu elektronów między elektrodą a gatunkiem analitu w roztworze. Prąd jest mierzony przed i po każdym impulsie napięcia, a różnica między tymi dwiema wartościami prądu daje prąd różnicowy, który jest wykreślany w stosunku do przyłożonego potencjału. Wielkość tego prądu jest proporcjonalna do stężenia elektroaktywnych gatunków obecnych w roztworze. DPV oferuje zalety, takie jak doskonała rozdzielczość i względna bezwładność w stosunku do prądów pojemnościowych. Podczas gdy pierwszy umożliwia rozróżnienie wielu gatunków obecnych w roztworze, drugi pomaga zaciemnić sygnał w innych technikach woltamperometrii.

 Woltamperometria fali kwadratowej stosuje połączony potencjał fali kwadratowej i schodkowy do stacjonarnej elektrody. Podczas impulsów katodowych analit ulega redukcji na powierzchni elektrody, podczas gdy podczas impulsów anodowych kształtu fali zredukowany analit jest ponownie utleniany. Polarogram fali kwadratowej przedstawia różnicę prądu między dwoma punktami na woltamperogramie fali kwadratowej. Zazwyczaj punkty te są wybierane na szczycie prądu anodowego i katodowego. Różnica w prądzie między szczytami anodowym a katodowym w polerogramie z falą prostokątną jest proporcjonalna do stężenia analitu.

Techniki woltamperometrii: Woltamperometria impulsowa

Woltamperometria różnicowo-impulsowa (DPV) to rodzaj woltamperometrii, który polega na zastosowaniu serii impulsów napięciowych do ogniwa elektrochemicznego podczas pomiaru ...

voltammetric-techniques-pulse-voltammetry

Education

JoVE Core

Analytical Chemistry

Chemia analityczna

Unit 1

Jednostka 1

Electrochemical Analyses and Redox Titration

Analizy elektrochemiczne i miareczkowanie redoks

electrochemical-analyses-and-redox-titration

KEY TERMS AND CONCEPTS

KLUCZOWE TERMINY I POJĘCIA

pulse voltage methods for electrochemistry

Pulse voltage methods in electrochemistry use small, timed changes in voltage to measure current. Differential-pulse voltammetry, or DPV, adds short potential pulses to a linear sweep across an electrochemical cell. These pulses are usually in the millivolt range and appear at regular intervals. Each pulse lasts only a few milliseconds.

DPV works by creating faradaic current at the electrode surface. Faradaic current comes from redox reactions, where electrons move between the electrode and analyte species in solution. The current is measured before and after each pulse. The difference between those two values gives the differential current, which is plotted against the applied potential.

The size of the differential current is proportional to the concentration of the electroactive species in the solution. DPV also offers excellent resolution. That makes it easier to tell multiple species apart. It is also relatively inert to capacitive currents, which can hide signals in other voltammetry methods.

Square wave voltammetry uses a different pulse pattern. It applies a square wave together with a staircase potential at a stationary electrode. During the cathodic pulses, the analyte is reduced at the electrode surface. During the anodic pulses, the reduced analyte is reoxidized.

The square wave polarogram shows the current difference between two points in the square wave voltammogram. These points are usually taken at the peaks of the anodic and cathodic currents. The difference between those peaks is proportional to the concentration of the analyte.

Pulse Voltage Methods for Electrochemistry

pulse-voltage-methods-for-electrochemistry

electrochemistry: overview

Electrochemistry and Redox Reactions

Electrochemistry connects electrical measurements with chemical reactions, especially oxidation and reduction. It focuses on how electron movement helps explain reaction behavior. Oxidation is the loss of electrons from a substance, and reduction is the gain of electrons. A species with strong electron affinity is an oxidizing agent, or oxidant. A species that donates electrons is a reducing agent, or reductant. These redox steps are often described with half-reactions. When electrons move...

electrodes: overview

Types of Electrodes in Electrochemistry

Electrodes are conductive materials in an electrochemical cell. They allow electron transfer reactions to happen at their surfaces. Electrochemical measurements use them to control and measure current and potential. The working electrode, also called the indicator electrode, is the main sensing electrode. Its potential changes with the analyte concentration and with the activity of the electroactive species. Common indicator electrodes include inert platinum electrodes, silver electrodes that...

interfacial electrochemical methods: overview

interfacial-electrochemical-methods-overview

Static and Dynamic Electrochemical Methods

Static and dynamic electrochemical methods study what happens at the boundary between an electrode and a solution. These interfacial methods focus on the electrode-solution interface rather than the overall properties of the liquid. They are useful in electroanalytical chemistry because they can detect very small changes in analyte concentration. These methods are grouped by whether a nonzero current flows through the cell. Static methods, such as potentiometry, measure the cell potential...

potentiometry: overview

Potentiometry and Electrochemical Cell Potential

Potentiometry measures the potential difference between two electrodes in an electrochemical cell. It does this without drawing significant current, so the solution’s composition is not altered. The method uses an indicator electrode, which exchanges electrons with the analyte solution, and a reference electrode, which keeps a constant potential. Each electrode is placed in a solution that makes up a half-cell. In a common setup, the reference electrode is the anode, or left-hand electrode,...

potentiometry: types of electrodes

Reference and Indicator Electrodes in Potentiometry

Potentiometric measurements use reference electrodes and indicator electrodes to track changes in a solution. A reference electrode gives a stable baseline, while indicator and working electrodes respond to changes in the solution’s composition. The Standard Hydrogen Electrode, or SHE, is a common reference electrode. It keeps a zero potential at all temperatures. However, it needs a continuous supply of hydrogen gas, so it is not practical for routine use. The Saturated Calomel Electrode, or...

potentiometry: membrane electrodes

Membrane Electrodes in Ion Sensing

Membrane electrodes measure ions by using a selective membrane that creates a potential difference across it. This membrane potential is called the asymmetry potential, and it can remain nonzero even when analyte concentrations are the same on both sides of the membrane. The signal usually depends on all ions in the sample that can interact with the membrane, not just one analyte. Selectivity is described by a selectivity coefficient. This value compares the response to an interferent with the...

redox titration: overview

Redox Titration Endpoints and Indicators

Redox titration uses electron transfer in a redox, or reduction-oxidation, reaction to find the concentration of an unknown solution. The titrant has a known concentration, and it is added gradually to the analyte, which is the solution being tested. The endpoint shows when the reaction between the two substances is complete. Before a redox titration begins, the analyte should be in a single oxidation state. If needed, this is done by pre-oxidizing or pre-reducing the sample with an auxiliary...

redox titration: iodimetry and iodometry

Using Iodine to Find Unknown Concentrations

Iodometry and iodimetry use iodine to measure unknown concentrations in redox titrations. These methods help determine the amount of an oxidizing or reducing agent in a sample. The key idea is that iodine changes color and reacts in a known stoichiometric ratio with the analyte. In iodometric titrations, the sample usually contains an oxidizing agent. The solution is acidified and then treated with an excess of iodide ions, which releases an equivalent amount of iodine in equilibrium with...

redox titration: other oxidizing and reducing agents

redox-titration-other-oxidizing-and-reducing-agents

Choosing Oxidizing Titrants in Redox Titration

Redox titrations can use oxidizing titrants other than iodine. Common choices include potassium permanganate (KMnO4), cerium(IV), and potassium dichromate (K2Cr2O7). The best titrant depends on stability, cost, analyte strength, and the reaction rate between the analyte and the titrant. Potassium permanganate is a strong oxidizing titrant in highly acidic solution. It reduces from Mn(VII) to Mn(II) while it oxidizes the analyte to a higher oxidation state. KMnO4 also works as a self-indicator,...

potentiometric titration: overview

Endpoint Detection in Potentiometric Titration

Potentiometric titration is a quantitative analytical method used to find the concentration of an analyte by measuring the potential difference between two electrodes in a solution. The endpoint is the point where this potential changes sharply. It usually appears when the stoichiometric reaction between the analyte and the titrant is complete. To find the endpoint, the measured potential difference is plotted against the volume of titrant added. This graph is called a titration curve. A...

end point prediction: gran plot

Gran Plot for Titration Endpoint Prediction

A Gran plot helps predict the endpoint of a potentiometric or acid-base titration before the endpoint is reached. It uses titration data collected only up to a point that is still below the equivalence volume. The data are then transformed into a straight-line format. To build the plot, the line is extended to the x-axis. That x-intercept shows the titrant volume needed to reach the equivalence point. In potentiometric titration, the Gran plot uses the volume-corrected base-10 antilogarithm of...

electrogravimetric analysis: overview

Electrode Weighing in Electrogravimetric Analysis

Electrogravimetric analysis measures an analyte by weighing the material that deposits on an electrode. A pre-weighed working electrode is placed in solution, and a potential is applied. The target substance then deposits by reduction at the cathode or by oxidation at the anode. After electrolysis, the electrode is weighed again. The mass increase gives the weight of the analyte in the solution. To check that deposition is complete, the fresh electrode surface is exposed to the solution while...

coulometry: overview

Coulometry and Electrical Charge Analysis

Coulometry is an analytical method that finds the amount of an analyte by measuring the electrical charge needed for its complete electrolysis. It is known for being rapid, accurate, and precise. Unlike many other methods, it does not require analytical standards. The total charge passed during electrolysis is linked to the amount of analyte through Faraday's laws of electrolysis. For correct coulometric measurements, the charge supplied must match Faraday's constant multiplied by the number...

controlled-potential coulometry: electrolytic methods

controlled-potential-coulometry-electrolytic-methods

Measuring Analyte Charge by Potentiostatic Coulometry

Controlled-potential coulometry measures analyte amount by carefully controlling electrode potential during electrolysis. It is also called potentiostatic coulometry. A potentiostat keeps the working electrode at a set potential in a three-electrode system. The working electrode choice depends on the potential range. Platinum working electrodes are used for positive potentials. Mercury pool electrodes are preferred for very negative potentials. The platinum counter electrode is kept away from...

controlled-current coulometry: overview

Controlled-Current Coulometry in Redox Analysis

Controlled current coulometry is an electrochemical method used to measure the amount of a substance by passing a steady current through a cell. It is also called amperostatic coulometry. The analyte, or substance being analyzed, reacts at the electrode surface as charge moves through the system. The amount of analyte is found by measuring how long it takes for a known charge to pass. This calculation follows Faraday’s laws of electrolysis. A typical setup includes a galvanostat, a...

controlled-current coulometry: coulometric titration

controlled-current-coulometry-coulometric-titration

Electrically Generated Reagents in Titration

Coulometric titrations use an electrically generated reagent to measure the amount of a substance in a sample. The electron acts as the standard reagent, and the result depends on the current and the time used to generate it. The method follows the same basic idea as a regular titration, including endpoint detection. Two conditions are essential for this type of titration. First, the electrode reaction that makes the reagent must be 100% efficient. Second, the generated reagent must react...

voltammetry: overview

Voltammetry for Detecting Redox Species

Voltammetry measures current in an electrochemical cell as the applied potential changes. It is an electroanalytical method used to study redox-active species. The current response is shown on a graph called a voltammogram. A voltammetric cell uses three electrodes: a working electrode, a reference electrode, and an auxiliary electrode. Redox reactions happen at the working electrode, and a potentiostat controls its potential. The reference electrode, such as a saturated calomel electrode or a...

voltammetry: factors affecting measurements

voltammetry-factors-affecting-measurements

Voltammetry and Faradaic Current

Voltammetry measures faradaic current, which is the current created by redox reactions of an analyte at the working and auxiliary electrodes. The current from reduction is called cathodic current and carries a positive charge. The current from oxidation is called anodic current and has a negative charge. The applied potential at the working electrode controls the flow of faradaic current. The size of that current depends on how fast the oxidation or reduction reaction occurs at the electrode...

voltammograms: overview

Voltammogram Shapes and Redox Analysis

Voltammograms are current plots made against applied potential. They help show how an electrochemical system behaves during a redox reaction. The shape of the plot depends on how the current is measured and on whether convection, or fluid movement, is present. When convection is present, as in hydrodynamic voltammetry, the voltammogram usually has a sigmoid shape. In this case, the current rises from a residual current to a limiting current at the analyte’s oxidation or reduction potential.

voltammetric techniques: linear-scan (e vs time)

voltammetric-techniques-linear-scan-e-vs-time

Polarography and Voltammetry with Mercury Drops

Polarography and hydrodynamic voltammetry are voltammetric techniques used to study electrochemical reactions. They track the current that flows as the electrode potential changes. In polarography, the key working electrode is a dropping mercury electrode, or DME. A DME uses a capillary tube filled with mercury. A tiny mercury droplet forms at the tip and then drops away. This gives a fresh electrode surface for each measurement. During the test, the potential applied to the DME changes...

voltammetric techniques: pulse voltammetry

Pulse voltage methods in electrochemistry use small, timed changes in voltage to measure current. Differential-pulse voltammetry, or DPV, adds short potential pulses to a linear sweep across an electrochemical cell. These pulses are usually in the millivolt range and appear at regular intervals. Each pulse lasts only a few milliseconds. DPV works by creating faradaic current at the electrode surface. Faradaic current comes from redox reactions, where electrons move between the electrode and...

voltammetric techniques: cyclic voltammetry

voltammetric-techniques-cyclic-voltammetry

Reading Redox Peaks with Cyclic Voltammetry

Cyclic voltammetry measures how current changes as the potential at an electrode is varied. It is used to study the redox properties of a chemical species, meaning how easily it is oxidized or reduced. The setup uses three electrodes in an electrolyte solution. The working electrode is where the redox reaction of interest takes place. The reference electrode provides a stable potential, and the counter electrode completes the circuit for current flow. The process starts at a chosen initial...

voltammetry: stripping methods

Trace Analysis by Stripping Voltammetry

Stripping voltammetry is an electrochemical method used to detect trace amounts of analytes in solution. It works by applying a potential to an electrode and measuring the current that results. The current is then used to estimate the analyte concentration. Anodic Stripping Voltammetry, or ASV, is used for metals and metalloids at very low levels. It has two main steps: deposition and stripping. First, a negative potential reduces analyte ions and deposits them on the working electrode surface.

amperometry: overview

Measuring Analytes with Amperometric Sensors

Amperometry measures specific analytes in a solution by tracking the electric current from an electrochemical reaction. A constant potential is applied between a working electrode and a reference electrode. The current that results is proportional to the analyte concentration. The Clark oxygen electrode is a common example of amperometry. It uses a cathode and an anode sealed inside a gas-permeable membrane. The cathode is typically platinum or gold, and the anode is silver. When a potential...

key terms and concepts

Learn how differential-pulse and square wave voltammetry use timed voltage pulses to measure current, separate signals, and estimate analyte concentration.

Pulse Voltage Methods for Electrochemistry | JoVE K12

analytical chemistry

JoVE Core Analytical Chemistry simplifies complex chemical principles by breaking them down into clear, engaging animations, making topics from SI Units to NMR spectroscopy more accessible and straightforward. Additionally, the scientist-in-action videos highlight the application of these concepts in real-world research conducted in laboratories globally.

Pulse Voltage Methods for Electrochemistry

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