Name: raman and ir spectroelectrochemical methods as tools to analyze conjugated organic compounds
Uploaded: 2018-10-12T12:30:00.000+00:00
Duration: 9 min 11 s
Description: Watch this Scientific Journal Video about Raman and IR Spectroelectrochemical Methods as Tools to Analyze Conjugated Organic Compounds at JoVE.com

The research leading to these results has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sk&#322;odowska-Curie grant agreement No 674990 (EXCILIGHT). We thank the networking action funded from the European Union's Horizon 2020 research and innovation programme under grant agreement No 691684.

1. Preparation of the Experiment
<ol>
	<li>Cleaning procedure24 
	NOTE: The typical spectroelectrochemical cell consists of a platinum mesh(wire) or ITO working electrode (WE), Ag/AgCl or Ag electrode as a reference electrode (RE) and platinum coil or wire as an auxiliary electrode (AE) (Figure 1). All electrodes must be cleaned before use.
	<ol>
		<li>Rinse a quartz ITO electrode with deionized water from the wash bottle. Then place it in an ultrasonic bath in a beaker filled with acetone for 15 minutes at room temperature and then in a beaker filled with isopropanol for the next 15 minutes. The higher ultrasound bath power that is used, the better result of cleaning.</li>
		<li>Let the electrode dry in the air.</li>
		<li>Burn platinum mesh or wire working electrode using a high-temperature torch (at least 500 &#176;C) until it gets red (approximately 1 min). Remove it from the fire, when it turns red and then cool it in the air to room temperature (approximately 1 min). Be careful to not melt the mesh electrode.</li>
		<li>Polish the gold working electrode with emery paper (grit 2000) and then with 1 &#181;m alumina. Ultrasonicate in deionized water for 5 minutes. Afterwards, rinse the electrode three times with the solvent used for the measurements. Use working electrodes directly after cleaning.</li>
		<li>Burn the active area of the auxiliary electrode (platinum wire or spiral) using a high-temperature gas torch (at least 500 &#176;C) until it gets red (approximately 1 min) and then cool in the air to room temperature.</li>
		<li>Take the reference electrode out from the storage electrolyte and wash it three times with the solvent used for the measurements.</li>
		<li>Clean the spectroelectrochemical vessel with alcohol (ethanol or isopropanol) or acetone using a syringe and air dry. Clean all other elements (i.e., Teflon parts) with acetone and air dry before use (minimum 1 minute).</li>
	</ol>
	</li>
	<li>Prepare at least 10 mL of the supporting electrolyte solution. The electrolyte solution should fulfil the same requirements as for standard electrochemical experiments, i.e., its concentration should be at least 100 times higher than the concentration of the analyte. An example electrolyte could be 0.2 M solution of Bu4NPF6 in dry acetonitrile or dichloromethane and a sample concentration of 1 mM. Water solutions, like 1 M H2SO4(aq), can be also used for Raman spectroscopy. If it is possible, use solvent and electrolyte of the highest purity.</li>
	<li>In the case of spectroelectrochemistry of an analyte present in solution, prepare at least 1 mL of an analyte solution at 1 mM concentration in the electrolyte solution.</li>
	<li>Put the argon (or nitrogen) Teflon pipe in the solution and start bubbling it for at least 5 min, in order to remove residual oxygen from the solution. Control the gas flow, so that only small bubbles appear at the solution surface. Do not use too high gas flow; otherwise, the solvent will evaporate from the vessel. In order to reduce solvent evaporation, a gas saturated with the solvent can be used. In this case, the inert gas must flow through a container with dry solvent before flowing to your electrolyte solution.</li>
</ol>
2. IR Spectroelectrochemistry
<ol>
	<li>Run electrochemical (cyclic voltammetry) tests on the analyte before starting the spectroelectrochemical analysis7, so that the potential range, in which the redox processes occur, or the reversibility of the redox processes, can be determined.</li>
	<li>Assemble the experimental cell equipped with three electrodes (working mesh platinum, auxiliary and reference) as presented in Figure 1. Ensure there is no leakage by filling it with the pure solvent. In the case of leakage, correct the mounting of the cell. When the cell is tight, remove the solvent with the syringe.</li>
	<li>Turn on the IR spectrometer and the corresponding software.</li>
	<li>Put the cuvette in the spectrometer holder. Fill the cuvette with the 2 mL of the analyte solution. The part of the working electrode, that will be irradiated with the incident beam, and the reference and auxiliary electrodes must be immersed in with the solution.</li>
	<li>Connect the electrodes with corresponding wires going from the potentiostat using crocodile clamps. Ensure to not short circuit the electrodes (they should not touch each other).</li>
	<li>Set the parameters of the spectra acquisition (spectrum range and resolution, the number of spectra to repeat in the case of FTIR). An example of typical parameters are as follows: spectrum range of 600-4000 cm-1, resolution of 1 cm-1, the number of spectra to repeat &#8211;&#160;16.</li>
	<li>Collect the IR spectrum by pressing the corresponding button on the spectrometer or in the software. Here, press the Background button to register a background and then press Scan button to collect spectrum.</li>
	<li>Using the connected potentiostat apply a potential of 0.0 V to the working electrode and collect the IR spectrum (press the Scan button). Save the spectrum giving it an appropriate filename.</li>
	<li>Change the applied potential, typically increase by a 100 mV, wait for app. 5 s, collect another IR spectrum and save it under the appropriate filename. Repeat this step until you reach entire potential range, in which oxidation/reduction processes may occur.</li>
	<li>In order to check the reversibility of the structural changes during electrochemical oxidation or reduction, return to an initial potential (0.0 V) and collect the IR spectrum again. Either apply an increment of 100 mV or go straight back to the initial potential.</li>
	<li>Subtract the initial spectrum from all other spectra to obtain differential spectra. Then, determine a straight line as the baseline by subtracting the neutral spectrum from itself in the software.
	<ol>
		<li>From the menu Process, chose Arithmetic.</li>
		<li>In the newly opened window (Arithmetic settings), chose the operator from the dropdown list Subtract (-).</li>
		<li>Select Operand and then select the spectrum registered at 0.0 V from the dropdown list.</li>
		<li>To confirm the operation, press OK.</li>
		<li>To export data to a spreadsheet, choose File | Send To | Excel.</li>
	</ol>
	</li>
	<li>When finishing the spectroelectrochemical measurement, register a CV of the solution (refer to point 2.1 of the protocol). Then add the appropriate amount of ferrocene to receive its concentration of app 0.5 mM and register the CV again. 
	NOTE: Ferrocene is used as a standard as its oxidation potential occurs at 4.8 eV. By recalculating the oxidation/reduction potentials of the sample vs. ferrocene, estimate the proper potential of the registered process and unify your data.</li>
</ol>
3. IR Spectroelectrochemistry in a Reflectance Mode
<ol>
	<li>Perform the same measurement procedure as for the transmission mode. The only difference is in the cell assembly (2.4) which is different for each kind of experimental cell.</li>
</ol>
4. Raman Spectroelectrochemistry
<ol>
	<li>Run the electrochemical (cyclic voltammetry) tests on the analyte before starting the spectroelectrochemical analysis7, so that the potential range, in which the redox processes occur, or the reversibility of the redox processes, can be determined.</li>
	<li>Deposit the layer of interest on the wire or plate electrode by electrochemical polymerization or by dip casting method12.</li>
	<li>Turn on the Raman spectrometer, laser and the corresponding software.</li>
	<li>Put the experimental cell together. Place the three electrodes (working, reference and auxiliary) in the cuvette, so that they do not touch each other, as presented in the Figure 2. The best is to use a Teflon holder, well-fitting the cuvette.
	<ol>
		<li>Place the working electrode (or working electrode covered with the deposited film) as close to the cuvette wall facing the incoming incident beam as possible, but do not press it to the wall (leave some space so the solution can flow easily between the cuvette wall and the working electrode).</li>
	</ol>
	</li>
	<li>Fill the cuvette with the electrolyte or analyte solution using a syringe (approximately 2 mL). Immerse all electrodes in the solution.</li>
	<li>Put the cuvette into the holder in the Raman spectrometer and connect the electrodes with corresponding wires going from the potentiostat using crocodile clamps. Ensure that electrodes or connectors do not touch each other.</li>
	<li>If the spectrometer is equipped with a camera, focus it onto the film deposited on the working electrode manually and/or using the software. A clear view of the working electrode surface should be visible.</li>
	<li>Close the spectrometer&#39;s cover.</li>
	<li>Choose the type of the laser desired and the corresponding grating based on the literature data or self-experience (for example the near infra-red 830 nm excitation laser and 1200 lines grating can be used). 
	NOTE: The higher energy of the incident beam light the more accurate spectra can be obtained, but also the greater risk of fluorescence, which prevents spectrum analysis. The choice of the grating type will change the range and/or resolution of acquired spectra. Typically, the most appropriate laser and grating can be selected by testing all available.</li>
	<li>Focus the laser beam on the working electrode surface using the software. If the spectrometer is equipped with a camera, the position at which the sharpest dot or line of the incident beam light on the sample is observed.</li>
	<li>Set the parameters of the spectra acquisition: laser power, spectral range, time of illumination of the sample etc. The choice of the parameters depends on the type of the film or/and the substrate and should be selected individually. Do not use too high laser power; otherwise the sample is destroyed. Example parameters are as follows: laser power - 1%, spectra range - 400-3200 cm-1, time of illumination - 1 s, measurement repeated 3 times.</li>
	<li>Collect the Raman spectrum by pressing the corresponding button on the spectrometer or in the software. If the intensity of the peaks on the registered spectra is weak, increase the power or acquisition time. A broadband in the spectra indicates the fluorescence phenomena. In this case, change the incident beam light to less energetic (higher wavelength) or try decreasing the laser power.</li>
	<li>Apply a potential of 0.0 V to the working electrode using the connected potentiostat and collect the Raman spectrum. Save the spectrum giving it an appropriate filename.</li>
	<li>Change the applied potential, typically increasing by 100 mV, wait for approximately 15 s, collect another spectrum and save it under the appropriate filename. Repeat this step until reaching the entire potential range where oxidation/reduction processes occur.</li>
	<li>In order to check the reversibility of the structural changes during electrochemical oxidation or reduction, return to the initial potential (0 V) and collect Raman spectrum again.</li>
	<li>When the spectroelectrochemical measurements are finished, register a CV of an analyte (present in solution or deposited on the electrode). Then, in the case of aprotic solutions, add the appropriate amount of ferrocene to obtain its concentration of app 0.5 mM and register the CV again. 
	NOTE: Ferrocene is used as a standard, as its oxidation potential occurs at 4.8 eV. By recalculating the oxidation/reduction potentials of the sample vs. ferrocene, the proper potentials of registered processes can be determined.</li>
</ol>

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S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Raman+Spectroelectrochemistry+of+a+Lithium/Polymer+Electrolyte+Symmetric+Cell.">Raman Spectroelectrochemistry of a Lithium/Polymer Electrolyte Symmetric Cell.</a> J Electrochem Soc. 145, 3034-3042 (1998).</li><li>Adar, F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Depth+Resolution+of+the+Raman+Microscope:+Optical+Limitations+and+Sample+Characteristics.+Spectroscopy.">Depth Resolution of the Raman Microscope: Optical Limitations and Sample Characteristics. Spectroscopy.</a> Spectroscopy. , (2018).</li></ol>

The authors have nothing to disclose.

Both IR and Raman techniques are recommended for the investigation of the structural changes occurring under applied potential and for the investigation of the products of the redox reaction. However, from the practical point of view, Raman spectroscopy is handier as an analytical tool in such experiments. Raman spectroelectrochemistry gives more possibilities, as it can be also applied to samples with nonpolar bonds. It has been therefore successfully used for the investigation of carbon materials, polymers, batteries, etc.29,30,31,32,33 Since the scattered light is measured substantially in Raman spectroscopy, there are generally no limits in the working electrode material or construction. Additionally, as used herein, incident light (UV-Vis-NIR) is poorly absorbed by the glass, which allows for the use of a standard electrochemical cell. The great advantage is also the possibility of conducting measurements outside the spectrometer through fiber optics. In order to register a Raman spectrum, the incident light needs to be properly focused on the sample. By focusing the light beam at different locations of the measuring cell, it can be decided if the changes in chemical composition occurring in the solution, e.g. near the electrode, or in the species adsorbed on the electrode surface are followed.
The use of Raman spectroscopy with an appropriate resolution also allows for the study of the profile of the solid samples, either on the surface or in its depths, also in the multi-layer structures.34,35,36,37 One can, therefore, get information about the surface topography, the distribution of different chemical species at the surface or in cross-section. Raman spectroelectrochemistry permits in situ tracking of the changes of all these features during redox processes and thus estimate the quality of the individual layers, the durability of the system during multiple oxidation/reduction cycles, or studying the diffusion in multilayer structures. The versatility of Raman spectroelectrochemistry lies in the fact that it can be used to examine both the electrochemical processes in a solution or solid state in a typical experimental cell or even test multilayer solid structures like LEDs, batteries, OPVs, etc.
The undoubted disadvantage of Raman spectroscopy and, thus also spectroelectrochemistry, is its limitation due to observed fluorescence, which often makes it impossible to analyze the spectrum. This phenomenon can be in some cases eliminated by changing the excitation wavelength or preliminary illumination - photo-bleaching.

The combination of electrochemical and spectroscopic techniques allows for the possibility of tracking the structural changes in molecules present at the electrode surface or in the solution, thus investigating the mechanism of the electrochemical processes. Spectroelectrochemical methods are typically used for the in situ study of the mechanism of the reaction. The undoubted advantage over ex situ measurements is the possibility of observing the signal arising for the intermediate products of processes or investigating the processes, in which products cannot be separated1. Among all spectroscopies, the Raman and infrared spectroscopies are the most powerful for analysis of electrochemical processes due to equipment availability and the often non-destructive nature of the measurements.
Infrared and Raman spectroscopies provide information about the vibrational structure of the species and thus the existing chemical bonds. Since the nature of the signals observed in both techniques is different, some vibrations may be active only in IR or Raman spectra, making them complementary to each other2. This should be taken into account, when planning spectroelectrochemical analysis and, if possible, the vibrational structure of an analyte should be examined using both IR and Raman spectroscopies. The best results are obtained when the changes in the structure are the result of the electrochemical process involving groups active in the certain technique. For example, the infrared spectroscopy would be ideal for processes involving -CO, -CN -NO or -NH groups&#39; formation or breakage3. It is always recommended to register differential spectra of the spectroelectrochemical investigation. Also, such spectra disclose changes in the signals with lower intensity allowing the tracking of changes in the structure of the aromatic systems. Additionally, differential spectra are always less complex as only changes are registered, which makes the interpretation of the spectra much easier.
IR spectroelectrochemical experiments are mainly used for the monitoring of the soluble products, intermediates and reactants of the electrochemical reactions; such tests may be run on various systems, including organic, inorganic, or biochemical systems3,4,5,6,7,8. One should always remember that in the case of IR spectroscopy, solvents in which hydrogen bonding occurs, like water, should be avoided.
There are several ways to proceed with IR and Raman measurements. In the case of IR spectroscopy, measurements can be done in the transmission mode, in which conventional IR cuvettes for liquids can be used. The optically transparent electrodes (e.g., boron-doped diamond electrode) or perforated electrodes (metal gauze working electrode) made of fine metal (Pt or Au) are usually used as the working electrodes in such transmission cells4,9. An example of the transmission spectroelectrochemical cell is presented in the Figure 1.
In the second technique, instead of transmission, the reflectance mode is applied, thanks to the ATR (Attenuated Total Reflection) attachment10. This method allows analyzing both solutions and solid-state materials. Typically when using the method of external reflection absorption spectroscopy, in principle, any working electrode can be used, but only dissolved species can be investigated. However, in some cases, the ATR technique allows also for the investigation of processes in the solid state, using the internal reflection method5,8. A special cell is required for this technique, in which the fine metal sputtered on the ATR crystal acts as a working electrode (Figure 2). In some cases, even the ATR Ge crystal itself can act as an electrode (at least for not too high currents)5.
The second technique is Raman spectroelectrochemistry; a technique combining both electrochemistry and Raman spectroscopy, commonly used in the investigation of the potentially-induced structural changes in the deposited layer of conjugated polymers11, like polyaniline12, polypyrroles13, polycarbazole14 or PEDOT15. Additionally to polymeric films, monolayers can be also tested19,20,21, though in this case metallic substrates, like gold or platinum, are preferred. The procedure of Raman spectroelectrochemical studies is analogical to other spectroelectrochemical techniques, i.e., a spectrometer must be coupled with a potentiostat and the spectra of the film are acquired in the potentiostatic conditions under various potentials&#39; applied18. Typically, the three-electrode spectroelectrochemical cell can be constructed based on the classical quartz cuvette with electrodes mounted in a Teflon holder (Figure 3). The acquisition parameters, like the type of the laser, grating, etc., depend on the properties of the investigated layer. Selection of some parameters can be quite difficult, e.g., one has to remember that various excitation wavelengths can result in different spectra. Usually, the higher energy of incident light the more details are visible on the spectrum, but also the higher risk of fluorescence phenomena that hinders the analysis. Generally, it is very useful to obtain the UV-Vis-NIR spectra of the analyte at first, in order to select the Raman excitation laser. The tunable lasers can be adjusted so that the excitation wavelength induces coincidence with an electronic transition of the molecule, resulting in the resonance Raman scattering. In this case, the increasing Raman scattering intensity in chosen regions of the spectra or even formation of new signals is observed that would not be registered typically. The analysis of the structural changes consists in the assignment of recorded Raman bands, which can be done based on the literature data or DFT simulations23.

<table><tbody><tr><td>Potentiostat</td><td>Metrohm</td><td>Autolab PGSTAT100</td><td></td></tr><tr><td>Raman microscope</td><td>Renishaw</td><td>inVia</td><td></td></tr><tr><td>FT-IR Spectrometer&amp;nbsp;</td><td>PerkinElmer&amp;nbsp;</td><td>Spectrum Two&amp;nbsp;</td><td></td></tr><tr><td>Bu4NBF4</td><td>Sigma-Aldrich</td><td>86896</td><td></td></tr><tr><td>DCM</td><td>Sigma-Aldrich</td><td>443484</td><td></td></tr><tr><td>Isopropanol</td><td>Sigma-Aldrich</td><td>675431</td><td></td></tr><tr><td>Acetone</td><td>Sigma-Aldrich</td><td>439126</td><td></td></tr></tbody></table>

raman and ir spectroelectrochemical methods as tools to analyze conjugated organic compounds

In the presented work, two spectroelectrochemical techniques are discussed as tools for the analysis of the structural changes occurring in the molecule on the vibrational level of energy. Raman and IR spectroelectrochemistry can be used for advanced characterization of the structural changes in the organic electroactive compounds. Here, the step-by-step analysis by means of Raman and IR spectroelectrochemistry is shown. Raman and IR spectroelectrochemical techniques provide complementary information about structural changes occurring during an electrochemical process, i.e. allows for the investigation of redox processes and their products. The examples of IR and Raman spectroelectrochemical analysis are presented, in which the products of the redox reactions, both in solution and solid state, are identified.

The structural changes of the monomer and polymer occurring during the doping are very useful to determine the mechanism of the process and for that, the IR spectroelectrochemical investigation can be conducted (Figure 4). In the example experiment, IR spectra were recorded in the differential form i.e. IR spectra of the investigated compound were taken as a reference. Such an approach allows for the exposure of the changes in the spectra occurring during polymerization: the disappearance of bonds are thus seen as a positive signal (increasing transmittance) while the formation of the new bonds is seen as negative peaks (decreasing transmittance) (Figure 4).
IR spectra recorded during analyte electropolymerization are shown in the Figure 4. As it can be seen, some changes occur at around 1600 cm-1, suggesting the disappearance of some of the material&#39;s double bonds. The most important are changes in the region between 700 - 900 cm-1: the increase in the transmittance at 750 and 675 cm-1 indicates the disappearance of the monosubstituted ring, simultaneously a new signal arising from the disubstituted ring appears around 830 cm-1. Based on the presented IR spectroelectrochemical experiment, the mechanism of the electropolymerization consisting in the reaction of the vinyl group with the free benzene ring is proposed.
In the presented example of Raman spectroelectrochemical studies, the potentially-induced structural changes of polyaniline film deposited on the electrografted layer of aniline (Figure 5) are investigated. The Raman spectra were recorded under potentiostatic conditions in the 1 M H2SO4 solution in the 800 - 1700 cm-1 range using 830 nm excitation laser and 1200 lines grating 25.
The Raman spectroelectrochemistry results of polyaniline electropolymerized on the electrografted gold substrate (PANi/amino/Au) are shown in the Figure 5. The signal assignment was based on the literature data11,26,27,28. At the starting potential of 0 mV, the bands at 1178 cm-1, 1265 cm-1 and 1608 cm-1 arising from the C-H in-plane bending, C-N stretching, and C-C stretching respectively, are observed and confirm that the polyaniline below the potential of A-redox couple exists in the leucoemeraldine form. The increase in the applied potential above the potential of the first redox couple (A) causes the formation of the C-N stretching bands at 1239 cm-1 and 1264 cm-1, and semiquinone polyaniline structure that is indicated by two overlapping peaks within the 1300-1420 cm-1 region. Further increase in the potential up to 500-700 mV, i.e. above the potential of the second redox couple (B), causes a correlated growth of three bands: at 1235 cm-1- C-N stretching, at 1483 cm-1- C=N stretching and at 1590 cm-1- C=C stretching, which are characteristic for the deprotonated quinoid ring. This is accompanied by the decrease in the relative intensity of the 1335 cm-1 band, indicating the transition of polyaniline into the pernigraniline form.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/56653/56653fig1.jpg" /> 
Figure 1: Scheme of transmission IR-spectroelectrochemistry cell (a) and its side view after assembly (b). <a href="/files/ftp_upload/56653/56653fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/56653/56653fig2.jpg" /> 
Figure 2: Schemes of reflectance cells for IR-spectroelectrochemistry. External reflectance cells a) and b) are used for the investigation of solute species. Internal reflectance cell c) is used for the investigation of species adsorbed on the electrode. <a href="/files/ftp_upload/56653/56653fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/56653/56653fig3.jpg" /> 
Figure 3: Schemes of Raman spectroelectrochemical cell <a href="/files/ftp_upload/56653/56653fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/56653/56653fig4v3.jpg" /> 
Figure 4: IR spectra of the monomer at various potentials applied <a href="/files/ftp_upload/56653/56653fig4v3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/56653/56653fig5.jpg" /> 
Figure 5: Raman spectra of polyaniline at a different potential; insert: CV curve recorded for the polyaniline film <a href="/files/ftp_upload/56653/56653fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Raman and IR Spectroelectrochemical Methods as Tools to Analyze Conjugated Organic Compounds at JoVE.com

Raman and IR Spectroelectrochemical Methods as Tools to Analyze Conjugated Organic Compounds

A protocol of step-by-step Raman and IR spectroelectrochemical analysis is presented.

In the presented work, two spectroelectrochemical techniques are discussed as tools for the analysis of the structural changes occurring in the molecule ...

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18.2K Views.  Silesian University of Technology. A protocol of step-by-step Raman and IR spectroelectrochemical analysis is presented.

Video: Raman and IR Spectroelectrochemical Methods as Tools to Analyze Conjugated Organic Compounds

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds

Cyclic voltammetry (CV) is a technique used in the analysis of organic compounds. When this technique is combined with electron paramagnetic resonance (EPR) or ultraviolet-visible and near-infrared (UV-Vis-NIR) spectroscopies, we obtain useful information such as electron affinity, ionization potential, band-gap energies, the type of charge carriers, and degradation information that can be used to synthesize stable organic electronic devices. In this study, we present electrochemical and spectroelectrochemical methods to analyze the processes occurring in active layers of an organic device as well as the generated charge carriers.

In this article, we describe electrochemical, electron paramagnetic resonance, and ultraviolet-visible and near-infrared spectroelectrochemical methods to analyze organic compounds for application in organic electronics.

Cyclic voltammetry (CV) is a technique used in the analysis of organic compounds. When this technique is combined with electron paramagnetic resonance ...

Ultrafast Time-resolved Near-IR Stimulated Raman Measurements of Functional &#960;-conjugate Systems

Femtosecond time-resolved stimulated Raman spectroscopy is a promising method of observing the structural dynamics of short-lived transients with near infrared (near-IR) transitions, because it can overcome the low sensitivity of spontaneous Raman spectrometers in the near-IR region. Here, we describe technical details of a femtosecond time-resolved near-IR multiplex stimulated Raman spectrometer that we have recently developed. A description of signal generation and optimization, measurement, data acquisition, and calibration and correction of recorded data is provided as well. We present an application of our spectrometer to analyze the excited-state dynamics of &#946;-carotene in toluene solution. A C=C stretch band of &#946;-carotene in the second lowest excited singlet (S2) state and the lowest excited singlet (S1) state is clearly observed in the recorded time-resolved stimulated Raman spectra. The femtosecond time-resolved near-IR stimulated Raman spectrometer is applicable to the structural dynamics of &#960;-conjugate systems from simple molecules to complex materials.

Details of signal generation and optimization, measurement, data acquisition, and data handling for a femtosecond time-resolved near-IR stimulated Raman spectrometer are described. A near infrared stimulated Raman study on the excited-state dynamics of &#946;-carotene in toluene is shown as a representative application.

Femtosecond time-resolved stimulated Raman spectroscopy is a promising method of observing the structural dynamics of short-lived transients with near ...

Raman Spectroscopy for Chemical Analysis

Source: Laboratory of Dr. Ryoichi Ishihara &#8212; Delft University of Technology
Raman spectroscopy is a technique for analyzing vibrational and other low frequency modes in a system. In chemistry it is used to identify molecules by their Raman fingerprint. In solid-state physics it is used to characterize materials, and more specifically to investigate their crystal structure or crystallinity. Compared to other techniques for investigating the crystal structure (e.g. transmission electron microscope and x-ray diffraction) Raman micro-spectroscopy is non-destructive, generally requires no sample preparation, and can be performed on small sample volumes.
For performing Raman spectroscopy a monochromatic laser is shone on a sample. If required the sample can be coated by a transparent layer which is not Raman active (e.g., SiO2) or placed in DI water. The electromagnetic radiation (typically in the near infrared, visible, or near ultraviolet range) emitted from the sample is collected, the laser wavelength is filtered out (e.g., by a notch or bandpass filter), and the resulting light is sent through a monochromator (e.g., a grating) to a CCD detector. Using this, the inelastic scattered light, originating from Raman scattering, can be captured and used to construct the Raman spectrum of the sample.
In the case of Raman micro-spectroscopy the light passes through a microscope before reaching the sample, allowing it to be focused on an area as small as 1 &#181;m2. This allows accurate mapping of a sample, or confocal microscopy in order to investigate stacks of layers. Care has to be taken, however, that the small and intense laser spot does not damage the sample.
In this video we will briefly explain the procedure for obtaining a Raman spectra, and an example of a Raman spectrum captured from carbon nanotubes will be given.

Source: Laboratory of Dr. Ryoichi Ishihara &#8212; Delft University of Technology
Raman spectroscopy is a technique for analyzing vibrational and other ...

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Infrared Spectroscopy

Source: Vy M. Dong and Zhiwei Chen, Department of Chemistry, University of California, Irvine, CA
This experiment will demonstrate the use of infrared (IR) spectroscopy (also known as vibrational spectroscopy) to elucidate the identity of an unknown compound by identifying the functional group(s) present. IR spectra will be obtained on an IR spectrometer using the attenuated total reflection (ATR) sampling technique with a neat sample of the unknown.

Infrared Spectroscopy: Characterization of Functional Groups

Source: Vy M. Dong and Zhiwei Chen, Department of Chemistry, University of California, Irvine, CA
This experiment will demonstrate the use of infrared ...

Organic Chemistry II

Infrared (IR) Spectroscopy: Overview

When electromagnetic radiation passes through a material, atoms or molecules transition from a lower to a higher energy state by absorbing radiation corresponding to the energy difference between the two states. The absorption of infrared (IR) radiation causes transitions between vibrational energy levels in a molecule. Therefore, IR spectroscopy is a useful analytical tool for determining the molecular structure of molecules.
Different compounds display unique properties due to their functional groups, which allows IR spectroscopy to be used to determine the present functional groups. Vibrational IR spectroscopy is performed in the 2.5 to 25 &#181;m wavelength range. A&#160; molecule is considered IR active if it exhibits a change in dipole moment during vibration when absorbing IR radiation. For a molecule to absorb IR radiation effectively, its vibrations must fluctuate its dipole moments, allowing it to interact with the electromagnetic field of the IR light.
Since different functional groups absorb IR radiation at varying frequencies, the IR spectrum is similar to the &#34;fingerprint&#34;&#160;for each molecule. IR spectroscopy is primarily employed in qualitative analysis to identify the functional groups in organic and inorganic compounds by comparing their vibrational frequencies with known compounds. Additionally, It can determine the concentration of a substance by applying the Beer-Lambert law, where absorbance is proportional to concentration.

Spektroskopia w podczerwieni (IR): przegląd

When electromagnetic radiation passes through a material, atoms or molecules transition from a lower to a higher energy state by absorbing radiation ...

KEY TERMS AND CONCEPTS

Spektroskopia w podczerwieni (IR): Przegląd

IR and UV&ndash;Vis Spectroscopy of Aldehydes and Ketones

Infrared spectroscopy, also known as vibrational spectroscopy, is mainly used to determine the types of bonds and functional groups in molecules. In aldehydes and ketones, the carbonyl (C=O)&#160;bond shows an absorption around 1710 cm-1. The C=O bond vibration of an aldehyde occurs at lower frequencies than that of a ketone. In addition to the C=O absorption in an aldehyde, the aldehydic C&#8211;H bond also gives two peaks in the 2700&#8211;2800 cm-1 range. This absorption, coupled with the C=O stretching, is characteristic of an aldehydic group.
Conjugation reduces the electron density in the C=O bond, thereby reducing its stretching frequency. The stretching frequencies of cyclic ketones vary depending on their ring sizes. The strain in larger rings is lower than in smaller cyclic ketones. Stretching frequency increases with increasing ring strain. Therefore, the smallest and highly strained cyclopropanone ring has the highest stretching frequency.
UV-Visible spectroscopy employs UV and visible light to transition between different electronic energy levels. Two major transitions in organic compounds are n to &#960;* and &#960; to &#960;* transitions. The &#960;&#8211;&#960;* is a stronger transition but occurs below 200 nm, which is not detectable in UV-Vis spectrometers. Conjugation of these molecules with a double bond or an aromatic ring shifts the absorption wavelength to above 200 nm. Each double bond that is conjugated adds a value of 30 nm to the absorption wavelength of the molecule.
n&#8211;&#960;* transition is weaker than &#960;&#8211;&#960;* transition. Since the non-bonding orbital on oxygen and the anti-bonding &#960;* orbital on the C&#8211;O bond is perpendicular, no overlap occurs between these two orbitals. Hence the n&#8211;&#960;* is a forbidden transition and occurs much less frequently.

IR and UV&amp;#8211;Vis Spectroscopy of Aldehydes and Ketones

Spektroskopia aldehydów i ketonów w podczerwieni i UV-VIS

Infrared spectroscopy, also known as vibrational spectroscopy, is mainly used to determine the types of bonds and functional groups in molecules. In ...

Organic Chemistry

Aldehydes and Ketones

IR and UV&ndash;Vis Spectroscopy of Carboxylic Acids

In IR spectroscopy of carboxylic acids, the C=O bond shows a characteristic band between 1710 and 1760 cm&#8315;&sup1;, and the O&#8211;H bond exhibits a broad band between 2500 and 3300 cm&#8315;&sup1;.
However, the stretching absorptions for the C=O bond vary depending on the structure of carboxylic acids. The C=O bond of the free carboxylic acids shows a higher stretching frequency, 1760 cm&#8722;1, while H-bonded carboxylic acids (dimers) exhibit stretching absorptions at a lower frequency, 1710 cm&#8722;1. The C=O bond of the conjugated aliphatic and aromatic carboxylic acids shows an even lower stretching frequency at 1690 cm&#8722;1.
In IR spectra of carboxylic acids, the stretching absorptions for the C&#8211;H and O&#8211;H bonds overlap and exhibit absorption around 3000 cm&#8722;1, having sharp C&#8211;H peaks and a broad O&#8211;H peak. Many carboxylic acids also exhibit small spikes or shoulder bands between 2500 and&#160; 2700 cm&#8722;1.
UV&ndash;vis spectroscopy of the carboxylic acids shows a weak band at a lower wavelength of 200&#8211;215 nm due to an n&#8594;&#960;&#8727; transition. However, in highly conjugated carboxylic acids, the n&#8594;&#960;&#8727; transition shifts to a higher wavelength with higher molar absorptivity.

IR and UV&#8211;Vis Spectroscopy of Carboxylic Acids

Spektroskopia IR i UV-VIS kwasów karboksylowych

In IR spectroscopy of carboxylic acids, the C=O bond shows a characteristic band between 1710 and 1760 cm&#8315;&sup1;, and the O&#8211;H bond exhibits a ...

Carboxylic Acids

Spectroscopy of Carboxylic Acid Derivatives

Infrared spectroscopy is primarily used to determine the types of bonds and functional groups. In carboxylic acid derivatives, a typical carbonyl bond absorption is observed around 1650&#8211;1850 cm&#8722;1. For esters, the absorption is recorded at around 1740 cm&#8722;1, while acid halides show the absorption at about 1800 cm&#8722;1. Another acid derivative, the acid anhydrides, exhibit two carbonyl absorption around 1760 cm&#8722;1 and 1820 cm&#8722;1, arising from the symmetrical and unsymmetrical carbonyl vibration.
In the case of nitriles, the polar carbon&#8211;nitrogen triple bond stretching produces a strong absorption at a higher frequency, around 2200 cm&#8722;1. In comparison, the carbonyl stretching of an amide occurs at a lower frequency, around 1660 cm&#8722;1, which can be attributed to the conjugation effect. Conjugation in the carbonyl compounds delocalizes the &pi; electrons, inducing a partial single bond character. Consequently, the bond requires less energy to stretch and absorbs at lower frequencies.
Interestingly, decreasing ring size in cyclic derivatives increases the ring strain, thereby increasing carbonyl absorption frequency.
The 1H NMR spectra of carboxylic acid derivatives show a peak around 10&#8211;12 ppm for highly shielded acidic protons, and the peak for the protons of the &alpha; carbon is observed around 2&#8211;2.5 ppm. In the 13C NMR spectra, the carbonyl carbon shows a distinct peak around 160&#8211;185 ppm. The absorption of the nitrile carbon is observed at a lower frequency.

Spektroskopia pochodnych kwasów karboksylowych

Infrared spectroscopy is primarily used to determine the types of bonds and functional groups. In carboxylic acid derivatives, a typical carbonyl bond ...

Carboxylic Acid Derivatives

UV&ndash;Vis Spectroscopy of Conjugated Systems

Organic compounds with conjugated double bonds show strong absorption features in the UV&ndash;visible region of the electromagnetic spectrum attributed to &#960;&VeryThinSpace;&#8594;&VeryThinSpace;&#960;* electronic excitations. Generally, a UV&ndash;vis absorption spectrum is recorded as a plot of absorbance vs wavelength. The wavelength of maximum absorbance, which manifests as a peak in the absorption spectrum, is denoted as &#955;max.
One of the factors influencing &#955;max is the extent of conjugation in the molecule. As shown below, an increase in conjugation shifts &#955;max to longer wavelengths.
<img alt="Figure1" src="/files/ftp_upload/12411/12411_PT_Figure_1.svg" style="text-align: center; height: 55px;" />
Highly conjugated &#960; systems absorb in the visible region rather than the UV and appear colored. The color reflected tends to be roughly complementary to the color that is absorbed. For example, lycopene, a compound found in tomatoes, absorbs in the blue region of the visible spectrum at 505 nm and reflects red, which is the perceived color.
<img alt="Figure2" src="/files/ftp_upload/12411/12411_PT_Figure_2.svg" style="text-align: center; height: 135px;" />

UV&amp;#8211;Vis Spectroscopy of Conjugated Systems

Spektroskopia UV–VIS układów sprzężonych

Organic compounds with conjugated double bonds show strong absorption features in the UV&ndash;visible region of the electromagnetic spectrum attributed ...

Raman and IR Spectroelectrochemical Methods as Tools to Analyze Conjugated Organic Compounds

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Infrared Spectroscopy

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