IR Signal Research Articles

Fast prediction of anharmonic vibrational spectra for complex organic molecules

Interpreting Raman and IR vibrational spectra in complex organic molecules lacking symmetries poses a formidable challenge. In this study, we propose an innovative approach for simulating vibrational spectra and attributing observed peaks to molecular motions, even when highly anharmonic, without the need for computationally expensive ab initio calculations. Our approach stems from the time-dependent stochastic self-consistent harmonic approximation to capture quantum nuclear fluctuations in atom dynamics while describing interatomic interaction through state-of-the-art reactive machine-learning force fields. Finally, we employ an isotropic charge model and a bond capacitor model trained on ab initio data to predict the intensity of IR and Raman signals.

Enhancing Mobility and Safety: A Smart Walking Cane for Visually Impaired Individuals with Ultrasonic Sensor, Infrared, and GSM Module

Traditionally, visually impaired individuals have relied on conventional walking canes to detect obstacles in their path. However, these canes have limitations in terms of efficiency. This paper focuses on the design and implementation of an electronic travel aid for visually impaired pedestrians, utilizing ultrasonic sensors, infrared technology, and a GSM module. The smart cane integrates ultrasonic sensors and IR technology to detect obstacles using ultrasonic waves and IR signals. When obstacles are detected, the sensor relays this information to a microcontroller (Atmega328P). The microcontroller processes the data and determines the proximity of the obstacle. If the obstacle is not closed, the system remains inactive. However, if the obstacle is close, the microcontroller activates a buzzer, generates continuous alarming sounds, and vibrates a motor, enabling the user to navigate the path more easily. Additionally, the system is equipped with a GSM module, allowing it to send SMS notifications to designated contacts in case of emergencies. By pressing an emergency button, a message is sent to a specified phone number. This integrated system provides both obstacle detection and emergency SMS notifications. The successful implementation of the system demonstrates its effectiveness and efficiency.

The Phenomenon of Vibrational Circular Dichroism Enhancement: A Systematic Survey of Literature Data.

While the intensity of vibrational circular dichroism (VCD) signals is commonly 104-105 times smaller than that of corresponding IR signals, several kinds of systems display enhanced VCD spectra with g-values (VCD/IR intensity ratio) above 10-3 and even reaching 5 × 10-2 in some exceptional cases. These systems include transition metal and lanthanide complexes, protein and peptide fibrils, short oligopeptide gels, crystalline compounds, gels and solution aggregates of organic compounds. We review the literature on VCD enhancement, focusing on collecting and analyzing data on enhanced g-values. Special attention is given to the mechanisms proposed to produce these effects.

A second-order kinetic model for global analysis of vibrational polariton dynamics.

The interaction between cavity photons and molecular vibrations leads to the formation of vibrational polaritons, which have demonstrated the ability to influence chemical reactivity and change material characteristics. Although ultrafast spectroscopy has been extensively applied to study vibrational polaritons, the nonlinear relationship between signal and quantum state population complicates the analysis of their kinetics. Here, we employ a second-order kinetic model and transform matrix method (TMM) to develop an effective model to capture the nonlinear relationship between the two-dimensional IR (or pump-probe) signal and excited state populations. We test this method on two types of kinetics: a sequential relaxation from the second to the first excited states of dark modes, and a Raman state relaxing into the first excited state. By globally fitting the simulated data, we demonstrate accurate extraction of relaxation rates and the ability to identify intermediate species by comparing the species spectra with theoretical ground truth, validating our method. This study demonstrates the efficacy of a second-order TMM approximation in capturing essential spectral features with up to 10% excited state population, simplifying global analysis and enabling straightforward extraction of kinetic parameters, thus empowering our methodology in understanding excited-state dynamics in polariton systems.

Working Voltage Switching the Photo-/Thermo-Electric Effect for Distinct Ultraviolet and Infrared Signal Detection.

The combination of sensing invisible ultraviolet photons and infrared radiation can significantly enhance target recognition by offsetting their own limit in a short sensing range and poor spatial resolution. However, the difference in their wavelength sets unique requirements for sensing materials and devices, which makes it hard to establish their implementation in a single detector. In this work, we present the design of a single detector with CH3NH3PbCl3 (MAPbCl3) for distinguishing ultraviolet and IR signals by switching its operating mode in the photo-/thermo-electric effect. The large optical band gap of ∼3.2 eV in MAPbCl3 ensures the response toward an ultraviolet photon, while its efficient thermoelectric effect allows the sensing of an IR signal. As a result, the detector exhibits a specific detectivity of 4.5 × 1012 Jones for 395 nm ultraviolet photons under 0 V, while under the working voltage of 2.5 V, it demonstrates a superior temperature coefficient of resistance of -3.7% K-1, a specific detectivity of 4.8 × 108 Jones, and a limit of detection of 0.58 mW/cm2 for 4 μm photons. The functionality of the switching response to ultraviolet or IR photons by working voltage allows background subtraction and enhances the target discrimination in the imaging.

The Fate of the Formic Acid Proton on the Anatase TiO2(101) Surface.

As a prototype adsorption reaction of gas Brønsted acid on oxides, we study the adsorption of formic acid on anatase. We perform infrared spectroscopy measurements of adsorbed HCOOH and HCOOD on TiO2 nanopowders, from 13 K up to room temperature in an ultra-high vacuum chamber. We assign the IR signals via computed spectra from nuclear quantum dynamics simulations using our divide-and-conquer semiclassical ab initio molecular dynamics method. The acid proton forms an extraordinarily short and strong hydrogen bond with the surface oxygen. The strength of this hydrogen bond, that compares to H bonds in ice at high pressures, is at the root of a substantial redshift with respect to the typical free OH stretching frequency, which eludes its straightforward detection.

Structures and dynamics of 8-oxo-7,8-dihydro-2'-deoxyguanosine in neutral and basic aqueous solutions by spectroscopy.

8-oxo-7,8-dihydro-2'-dexyoguanine (8-oxo-dG) can be tautomerized to a 6-enolate,8-keto tautomer through nearby-NH deprotonation at elevated pH. In this work, the N3-protonated 8-oxo-dG tautomers in deuterated pH-buffer solutions were studied using steady-state UV/Vis, FTIR, and ultrafast two-dimensional IR spectroscopies. The presence of 6,8-diketo and C6-anionic tautomers at neutral to basic conditions (pD = 7.4-12.0) was revealed by UV/Vis and FTIR results and was further confirmed by 2D IR signals in both diagonal and off-diagonal regions. However, the C6-enol tautomer, which may be an intermediate during the transition from 6,8-diketo to C6-enolate,C8-keto, was not observed appreciably due to its extreme low population. Furthermore, the neutral-to-anionic tautomeric transition of N3H-8-oxo-dG studied in this work occurs under more basic conditions than the N1H-8-oxo-dG reported previously, showing a higher pKa value for N3H than N1H. Finally, vibrational relaxation of the carbonyl stretching mode was found to be both molecular site dependent and pD dependent for 8oxo-dG. Taken together, this work shows that the ultrafast infrared spectroscopic method is effective for examining tautomers and their dynamics in nucleic acids.

Laser-irradiating infrared attenuated total reflection spectroscopy of articular cartilage: Potential and challenges for diagnosing osteoarthritis

ObjectiveA prototype infrared attenuated total reflection (IR-ATR) laser spectroscopic system designed for in vivo classification of human cartilage tissue according to its histological health status during arthroscopic surgery is presented. Prior to real-world in vivo applications, this so-called osteoarthritis (OA) scanner has been tested at in vitro conditions revealing the challenges associated with complex sample matrices and the accordingly obtained sparse spectral datasets. MethodsIn vitro studies on human knee cartilage samples at different contact pressures (i.e., 0.2–0.5 ​MPa) allowed recording cartilage degeneration characteristic IR signatures comparable to in vivo conditions with high temporal resolution. Afterwards, the cartilage samples were assessed based on the clinically acknowledged osteoarthritis cartilage histopathology assessment (OARSI) system and correlated with the obtained sparse IR data. ResultsAmide and carbohydrate signal behavior was observed to be almost identical between the obtained sparse IR data and previously measured FTIR data used for sparse partial least squares discriminant analysis (SPLSDA) to identify the spectral regions relevant to cartilage condition. Contact pressures between 0.3 and 0.4 ​MPa seem to provide the best sparse IR spectra for cylindrical (d ​= ​3 ​mm) probe tips. ConclusionLaser-irradiating IR-ATR spectroscopy is a promising analytical technique for future arthroscopic applications to differentiate healthy and osteoarthritic cartilage tissue. However, this study also revealed that the flexible connection between the laser-based analyzer and the arthroscopic ATR-probe via IR-transparent fiberoptic cables may affect the robustness of the obtained IR data and requires further improvements.

Amorphous 1-propanol interstellar ice beyond its melting point

ABSTRACT The recent discovery of 1-propanol (CH3CH2CH2OH) in the interstellar medium (ISM) is of tremendous interest since fatty alcohols have been proposed as constituents of proto-cell membranes. Motivated by this discovery, we present the laboratory mid-infrared (MIR) and vacuum ultraviolet (VUV) absorption spectra of 1-propanol ice under astrochemical conditions, mimicking an icy mantle on cold dust in the ISM. Both MIR and VUV spectra were recorded at ultrahigh vacuum of ∼10-9 mbar and at temperatures ranging from 10 K to sublimation. The morphology of the 1-propanol ice deposited at 10 K was amorphous. By warming the ice to temperatures of 140 K and above, with subsequent recording of IR spectra, we observe complete sublimation of 1-propanol molecules from the substrate around 170 K. No amorphous-to-crystalline phase change was observed upon warming to higher temperatures. Additionally, we observe the IR and VUV signatures of 1-propanol ice on the substrate well beyond its melting point (147 K). To the best of our knowledge, this is the first reported observation of a molecular ice staying well beyond its melting point under such conditions. This result shows that the morphology of icy mantles on ISM cold dust grains is more complex than previously thought. Our atomistic molecular dynamics simulations capture the experimental trends and shed light on the microscopic origin of this unusual phase behaviour of 1-propanol.

Correlated IR-SEM-TEM studies of three different grains from Ryugu: From the initial material to post-accretional processes

In order to better constrain the alteration history of the Ryugu parent body, we performed a multi-analytical study combining scanning electron microscopy, transmission electron microscopy and infrared spectroscopy on sections extracted from the three fragments A0064-FO019, A0064-FO021 and C0002-FO019 returned from Ryugu by the Hayabusa2 space mission. The three sections show large differences in terms of structure, mineralogy and infrared signature. Section A0064-FO019 resembles the major Ryugu lithology with the presence of both fine-grained phyllosilicates (fg-phyllos) with embedded nanosulfides and coarse-grained phyllosilicates (cg-phyllos), whereas section C0002-FO019 belongs to the group of the less altered lithologies with the presence of anhydrous minerals embedded in a partially amorphous matrix. Section A0064-FO021 also belongs to this group but shows two different lithologies, a compact amorphous one and a more porous and very fractured one showing the presence of Na-rich phosphate, calcite and olivine. The two less altered lithologies (sections A0064-FO021 and C0002-FO019) show the presence of numerous mineralogical features similar to those observed in cometary interplanetary dust particles, ultra-carbonaceous Antarctic micrometeorites or in the CM Paris meteorite, i.e. amorphous and partially crystallized matrix with GEMS-like ghosts objects, whisker olivine, phosphide, or FeNi metal. This supports an outer solar system origin common with that of cometary material for the Ryugu parent body. Combined with the results of Nakamura et al. (2022b) reporting the presence of a lithology showing the presence of GEMS-like objects, we propose that section C0002-FO019 represents the onset of aqueous alteration of such primitive materials. The cg-phyllos and fg-phyllos of section A0064-FO019, i.e. of the major Ryugu lithology, representing the advanced stage of alteration, exhibit distinctive IR signatures with a higher abundance of oxygen-rich functional groups in the organic matter (OM) from the cg-phyllos. We thus suggest the following chronology of formation and evolution for Ryugu: (1) accretion of highly porous aggregate of GEMS-like units with fine-grained high-temperature anhydrous silicates, (2) onset of alteration with the dissolution of primary nanosulfides and development of amorphous/partially crystallized material in the pores, (3) crystallization of fg-phyllos with a second generation of sulfides, (4) later formation of cg-phyllos devoid of nanosulfides and their associated oxygen-rich OM in a more water-rich environment.

Large-Scale, Mechanically Robust, Solvent-Resistant, and Antioxidant MXene-Based Composites for Reliable Long-Term Infrared Stealth.

MXene-based thermal camouflage materials have gained increasing attention due to their low emissivity, however, the poor anti-oxidation restricts their potential applications under complex environments. Various modification methods and strategies, e.g., the addition of antioxidant molecules and fillers have been developed to overcome this, but the realization of long-term, reliable thermal camouflage using MXene network (coating) with excellent comprehensive performance remains a great challenge. Here, a MXene-based hybrid network comodified with hyaluronic acid (HA) and hyperbranched polysiloxane (HSi) molecules is designed and fabricated. Notably, the presence of appreciated HA molecules restricts the oxidation of MXene sheets without altering infrared stealth performance, superior to other water-soluble polymers; while the HSi molecules can act as efficient cross-linking agents to generate strong interactions between MXene sheets and HA molecules. The optimized MXene/HA/HSi composites exhibit excellent mechanical flexibility (folded into crane structure), good water/solvent resistance, and long-term stable thermal camouflage capability (with low infrared emissivity of ≈0.29). The long-term thermal camouflage reliability (≈8 months) under various outdoor weathers and the scalable coating capability of the MXene-coated textile enable them to disguise the IR signal of various targets in complex environments, indicating the great promise of achieved material for thermal camouflage, IR stealth, and counter surveillance.

Thermal infrared observations of a western United States biomass burning aerosol plume

Abstract. Biomass burning smoke particles, due to their submicron particle size in relation to the average thermal infrared (TIR) wavelength, theoretically have negligible signals at the TIR channels. However, nearly instantaneous longwave (LW) signatures of thick smoke plumes can be frequently observed at the TIR channels from remotely sensed data, including at 10.6 µm (IR window), as well as in water-vapor-sensitive wavelengths at 7.3, 6.8, and 6.3 µm (e.g., lower, middle, and upper troposphere). We systematically evaluated multiple hypotheses as to causal factors of these IR signatures of biomass burning smoke using a combination of data from the Aqua MODerate resolution Imaging Spectroradiometer (MODIS), Aqua Cloud and the Earth Radiant Energy System (CERES), Geostationary Operational Environmental Satellite 16/17 (GOES-16/17) Advanced Baseline Imager, and Suomi-NPP Visible Infrared Imaging Radiometer Suite (VIIRS) and Cross-track Infrared Sounder (CrIS). The largely clear transmission of light through wildfire smoke in the near infrared indicates that coarse or giant ash particles are unlikely to be the dominant cause. Rather, clear signals in water vapor and TIR channels suggest that both co-transported water vapor injected to the middle to upper troposphere and surface cooling by the reduction of surface radiation by the plume are more significant, with the surface cooling effect of smoke aloft being the most dominant. Giving consideration of the smoke impacts on TIR and longwave, CERES indicates that large wildfire aerosol plumes are more radiatively neutral. Further, this smoke-induced TIR signal may be used to map very optically thick smoke plumes, where traditional aerosol retrieval methods have difficulties.

Ultrasensitive Plasmon-Enhanced Infrared Spectroelectrochemistry.

IR spectroelectrochemistry (EC-IR) is a cutting-edge operando method for exploring electrochemical reaction mechanisms. However, detection of interfacial molecules is challenged by the limited sensitivity of existing EC-IR platforms due to the lack of high-enhancement substrates. Here, we propose an innovative plasmon-enhanced infrared spectroelectrochemistry (EC-PEIRS) platform to overcome this sensitivity limitation. Plasmonic antennae with ultrahigh IR signal enhancement are electrically connected via monolayer graphene while preserving optical path integrity, serving as both the electrode and IR substrate. The [Fe(CN)6 ]3- /[Fe(CN)6 ]4- redox reaction and electrochemical CO2 reduction reaction (CO2 RR) are investigated on the EC-PEIRS platform with a remarkable signal enhancement. Notably, the enhanced IR signals enable a reconstruction of the electrochemical curve of the redox reactions and unveil the CO2 RR mechanism. This study presents a promising technique for boosting the in-depth understanding of interfacial events across diverse applications.

Ultrasensitive Plasmon‐Enhanced Infrared Spectroelectrochemistry

AbstractIR spectroelectrochemistry (EC‐IR) is a cutting‐edge operando method for exploring electrochemical reaction mechanisms. However, detection of interfacial molecules is challenged by the limited sensitivity of existing EC‐IR platforms due to the lack of high‐enhancement substrates. Here, we propose an innovative plasmon‐enhanced infrared spectroelectrochemistry (EC‐PEIRS) platform to overcome this sensitivity limitation. Plasmonic antennae with ultrahigh IR signal enhancement are electrically connected via monolayer graphene while preserving optical path integrity, serving as both the electrode and IR substrate. The [Fe(CN)6]3−/[Fe(CN)6]4− redox reaction and electrochemical CO2 reduction reaction (CO2RR) are investigated on the EC‐PEIRS platform with a remarkable signal enhancement. Notably, the enhanced IR signals enable a reconstruction of the electrochemical curve of the redox reactions and unveil the CO2RR mechanism. This study presents a promising technique for boosting the in‐depth understanding of interfacial events across diverse applications.

Vibrational Study of the Inward Proton Pump Xenorhodopsin NsXeR: Switch Order Determines Vectoriality

Common proton pumps, e.g. HsBR and PR, transport protons out of the cell. Xenorhodopsins (XeR) were the first discovered microbial rhodopsins which come as natural inward proton pumps. In this work we combine steady-state (cryo-)FTIR and Raman spectroscopy with time-resolved IR and UV/Vis measurements to roadmap the inward proton transport of NsXeR and pinpoint the most important mechanistic features. Through the assignment of characteristic bands of the protein backbone, the retinal chromophore, the retinal Schiff base and D220, we could follow the switching processes for proton accessibility in accordance with the isomerization / switch / transfer model. The corresponding transient IR signatures suggest that the initial assignment of D220 as the proton acceptor needs to be questioned due to the temporal mismatch of the Schiff base and D220 protonation steps. The switching events in the K-L and MCP-MEC transitions are finely tuned by changes of the protein backbone and rearrangements of the Schiff base. This finely tuned mechanism is disrupted at cryogenic temperatures, being reflected in the replacement of the previously reported long-lived intermediate GS* by an actual redshifted (O-like) intermediate.

An optimized purification protocol for enzymatically synthesized S-adenosyl-L-methionine (SAM) for applications in solution state infrared spectroscopic studies

S-adenosyl-L-methionine (SAM) is an abundant biomolecule used by methyltransferases to regulate a wide range of essential cellular processes such as gene expression, cell signaling, protein functions, and metabolism. Despite considerable effort, there remain many specificity challenges associated with designing small molecule inhibitors for methyltransferases, most of which exhibit off-target effects. Interestingly, NMR evidence suggests that SAM undergoes conformeric exchange between several states when free in solution. Infrared spectroscopy can detect different conformers of molecules if present in appreciable populations. When SAM is noncovalently bound within enzyme active sites, the nature and the number of different conformations of the molecule are likely to be altered from when it is free in solution. If there are unique structures or different numbers of conformers between different methyltransferase active sites, solution-state information may provide promising structural leads to increase inhibitor specificity for a particular methyltransferase. Toward this goal, frequencies measured in SAM’s infrared spectra must be assigned to the motions of specific atoms via isotope incorporation at discrete positions. The incorporation of isotopes into SAM’s structure can be accomplished via an established enzymatic synthesis using isotopically labeled precursors. However, published protocols produced an intense and highly variable IR signal which overlapped with many of the signals from SAM rendering comparison between isotopes challenging. We observed this intense absorption to be from co-purifying salts and the SAM counterion, producing a strong, broad signal at 1100 cm−1. Here, we report a revised SAM purification protocol that mitigates the contaminating salts and present the first IR spectra of isotopically labeled CD3-SAM. These results provide a foundation for isotopic labeling experiments of SAM that will define which atoms participate in individual molecular vibrations, as a means to detect specific molecular conformations.

A novel method to calibrate a fast IR-measurement system by utilizing the temperature dependence of oxide layers

Laser material processing by pulsed lasers is an effective method for realizing a variety of temperature-critical processes. Through appropriate parameter selection and processing strategies, micro-structuring can be used to functionalize material surfaces. One of these functionalization is the defined tempering of metallic surfaces to generate annealing colors. By locally heating the surface an oxide layer is formed that produces a specific color when exposed to light. This resulting color depends on its oxide layer thickness, which is determined by the temperature. Commonly this process is referred as laser coloring. In our present work we developed a new calibration method for a fast IR-emission measuring setup by utilizing the temperature dependence of the oxide layer. By using fast IR-detectors during laser coloring, it is possible to assign each measured IR signal to the resulting color and its corresponding temperature of the oxide layer, allowing a conversion to absolute temperatures.

Impact of UV radiation on the Raman and infrared spectral signatures of sulfates, phosphates and carbonates: Implications for Mars exploration

Perseverance is on Mars, collecting samples which will inform about Martian geology and paleoenvironmental conditions. However, the surface of Mars is continuously bombarded by ionizing and non-ionizing radiation, including UVs, which may significantly alter hydrated mineral phases such as sulfates, phosphates and carbonates. To explore and constrain this effect, we experimentally exposed pellets of more or less hydrated minerals to UV radiation within a Martian chamber at a temperature relevant for the rocks at the surface of Mars. Results show that exposure to UV leads to a strong alteration of the Raman and IR signals of sulfates, phosphates and carbonates. The strong increase of the luminescence signals coupled to the decrease of the Raman signals relatively to the background and the clear attenuation of the IR signals are interpreted as caused by an increasing concentration of electronic defects. The present results have major implications for the ongoing exploration of Mars: one should not expect to detect pristine materials, except over freshly excavated surfaces. Still, as a precaution, all the targets measured or collected on Mars should be considered as having been exposed to UV radiation to some extent.

Rapid discrimination of Lentilactobacillus parabuchneri biofilms via in situ infrared spectroscopy

Microbial contamination in food industry is a source of foodborne illnesses and biofilm-related diseases. In particular, biogenic amines (BAs) accumulated in fermented foods via lactic acid bacterial activity exert toxic effects on human health. Among these, biofilms of histamine-producer Lentilactobacillus parabuchneri strains adherent at food processing equipment surfaces can cause food spoilage and poisoning. Understanding the chain of contamination is closely related to elucidating molecular mechanisms of biofilm formation. In the present study, an innovative approach using integrated chemical sensing technologies is demonstrated to fundamentally understand the temporal behavior of biofilms at the molecular level by combining mid-infrared (MIR) spectroscopy and fluorescence sensing strategies. Using these concepts, the biofilm forming capacity of six cheese-isolated L. parabuchneri strains (IPLA 11151, 11150, 11129, 11125, 11122 and 11117) was examined. The cut-off values for the biofilm production ability of each strain were quantified using crystal violet (CV) assays. Real-time infrared attenuated total reflection spectroscopy (IR-ATR) combined with fluorescence quenching oxygen sensing provides insight into distinct molecular mechanisms for each strain. IR spectra showed significant changes in characteristic bands of amides, lactate, nucleic acids, and extracellular polymeric substances (i.e., lipopolysaccharides, phospholipids, phosphodiester, peptidoglycan, etc.), which are major contributors to biofilm maturation involved in the initial adhesion processes. Chemometric methods including principal component analysis and partial least square-discriminant analysis facilitated the rapid determination and classification of cheese isolated L. parabuchneri strains unambiguously differentiating the IR signatures based on their ability to produce biofilm. All biofilms were morphologically characterized by confocal laser scanning microscopy on relevant industrial equipment surfaces. In summary, this innovative approach combining MIR spectroscopy with luminescence sensing enables real-time insight into the molecular composition and formation of L. parabuchneri biofilms.

Dual-band absorption due to simultaneous excitation of TE and TM modes in ITO-ES metamaterial for IR stealth technology

We proposed a plasmonic based Indium Tin Oxide Embedded Silver (ITO-ES) infrared dual-band perfect absorber for the utilization in IR stealth technology. The proposed structure comprised of nano size Ag ring and desk embedded in ITO. The optical losses in optical regime of nanoscale plasmonic Ag were incorporated in terms of collision frequency using the modified Drude model. The optical response of the proposed structure was predicted by exciting it with a planwave using full wave vector frequency domain solver by employing Finite Element Method (FEM) in Computer Simulation Technology (CST) Microwave Studio. The simultaneous excitation of higher order transverse electromagnetic (TE and TM) modes in the proposed structure lead to high values of both absorption and Front to Back ratio (FTBR). The controlled and selective wavelength multiband absorption is crucial for IR stealth technology. The proposed metamaterial structures exhibit dual-bands IR absorption at wavelengths λ = 1.40 μm and 6.4 μm. First absorption peak suppresses the back scattering of the laser used by laser guided devices for detection, while the second peak suppresses the IR signature of the structure due thermal radiation which can be used by tracking devices to detect warm/hot objects.