Reflectance Infrared Research Articles

Assessing Mechanochemical Properties of Acrylonitrile Butadiene Styrene (ABS) Items in Cultural Heritage Through a Multimodal Spectroscopic Approach.

A multimodal spectroscopic approach is proposed to correlate the mechanical and chemical properties of plastic materials in art and design objects, at both surface and subsurface levels, to obtain information about their conservation state and to monitor their degradation. The approach was used to investigate the photo-oxidation of acrylonitrile butadiene styrene (ABS), a plastic commonly found in many artistic and design applications, using ABS-based LEGO bricks as model samples. The modifications of the chemical and viscoelastic properties of ABS during photoaging were monitored by correlative Brillouin and Raman microspectroscopy (BRaMS), combined with portable and noninvasive broad-range external reflection infrared (IR) spectroscopy and nuclear magnetic resonance (NMR) relaxometry, directly applicable in museums. BRaMS enabled combined measurements of Brillouin light scattering and Raman spectroscopy in a microspectroscopic setup, providing for the coincident probe of the chemical and mechanical changes of ABS at the sample surface. NMR relaxometry allowed for noninvasive measurements of relaxation times and depth profiles which are directly related to the molecular mobility of the material. Complementary chemical information was acquired by external reflection IR spectroscopy. The simultaneous probe of the chemical and mechanical properties by this multimodal spectroscopic approach enabled us to define a decay model of ABS in terms of compositional changes and variation of stiffness and rigidity occurring with photodegradation. The knowledge acquired on LEGO samples has been used to rate the conservation state of ABS design objects noninvasively investigated by external reflection Fourier transform IR spectroscopy and NMR relaxometry offered by the MObile LABoratory (MOLAB) platform of the European Research Infrastructure of Heritage Science.

Sustainable building envelopes: Evaluating the thermal performance of thatched roofs fabricated using coconut leaves

Excessive heat gain in residential buildings during sunny days, especially in tropical regions, leads to increased reliance on active energy cooling systems, contributing to higher carbon emissions and energy costs. Traditional roofing materials, such as terracotta tiles are often insufficient in mitigating indoor temperature rise, necessitating the exploration of alternative, sustainable solutions. This study investigates the thermal performance of naturally available coconut leaves used as thatch roofing, comparing it with conventional terracotta tiles, to determine their effectiveness in controlling interior temperatures and reducing heat gain in buildings. To mitigate such a problem, the Near Infra-Red (NIR) light reflectivity of dried plant leaves derived from deciduous and coniferous trees was measured. The structural hierarchy of the leaves was confirmed through Field Emission Scanning Electron Microscope (FESEM), Fourier Transform Infrared Spectroscope (FTIR) and X-ray Diffraction (XRD) studies. FTIR spectra reveal characteristic vibrations of ester, cellulosic components, etc., and XRD confirms the amorphous status of cellulosic materials present in the plant biomass. To study the use of thatched roofs made using coconut leaves as a roofing element, two test huts were fabricated - one was covered using terracotta roof tiles and the other was covered using coconut leaves thatches. The thermal performances of two roofing materials were recorded on a sunny day and the results were compared. The temperature data noticed reveal the fact that the maximum average surface temperature of the terracotta roof model was 59.53 °C, while the rooftop covered with coconut thatches exhibits a temperature of 54.26 °C which is 8.8% less than the hut covered with terracotta tiles. The interior temperature recorded in the coconut thatch was 33.36 °C, which was 1.15 °C lower (34.51 °C) than the terracotta tiles-covered test hut, confirming the better thermal comfortability of thatched roof model than a terracotta roof model.

Infrared Spectroscopy Study of Edge Water Penetration at Hydrophilic Bonding Interface

Hydrophilic wafer bonding is a process used to bond two wafers without adding material between the two surfaces. Water has a definite impact both during the bonding (bonding wave propagation, adhesion) (1) and after annealing (mechanical strength of the bonding interface, adherence) (2) during such a process. To have a better understanding of mechanisms ruling direct hydrophilic wafer bonding, it is thus important to quantify the amount of water present at the bonding interface.It is known that water is able to penetrate at the bonding interface at room temperature and 40% relative humidity. This has been demonstrated by analyzing defects with scanning acoustic microscopy (SAM) and from X-Ray Reflectivity (XRR) measurements (3,4). Kinetics observed by Tedjini et al. were consistent with a Lucas-Washburn flow through a one nm gap driven by the capillary forces of the hydrophilic surfaces.Nevertheless, no investigation of this phenomenon was performed using Fourier Transform Infra-Red Multiple Internal Reflection (FTIR-MIR) spectroscopy (5). Infrared spectroscopy of silanols, hydrogen bonded water and free water is well documented (6–8) and provides knowledge about water content and organization at the bonding interface. Here FTIR-MIR spectroscopy yields a direct measurement of the relative amount of water and its structure at the interface.More precisely this study will enable us to compare Si-Si, Si-SiO2 and SiO2-SiO2 water penetration kinetics at a fixed distance from the edge of the bonded substrates. A schematic view of the FTIR-MIR setup is shown in Figure 1 to explain the measurement principle.We report the study of water kinetics penetration at bonding interface by FTIR-MIR characterization. A Gaussian decomposition of the OH stretching absorption band signal allows identifying the contributions of silanols, surface bonded water and free liquid water as shown on Figure 2. The integral of each Gaussian peak is otherwise proportional to the relative amount of water. Surface preparation will be discussed and results compared to other characterizations techniques.REFERENCES Larrey V, Mauguen G, Fournel F, Radisson D, Rieutord F, Morales C, et al. Adhesion Energy and Bonding Wave Velocity Measurements. ECS Transactions. 23 sept 2016;75(9):145-52.Fournel F, Tedjini M, Larrey V, Rieutord F, Morales C, Bridoux C, et al. Impact of Water Edge Absorption on Silicon Oxide Direct Bonding Energy. ECS Transactions. 23 sept 2016;75(9):129-34.Tedjini M, Fournel F, Moriceau H, Larrey V, Landru D, Kononchuk O, et al. Interface water diffusion in silicon direct bonding. Appl Phys Lett. 12 sept 2016;109(11):111603.Rieutord F, Tardif S, Landru D, Kononchuk O, Larrey V, Moriceau H, et al. Edge Water Penetration in Direct Bonding Interface. ECS Trans. 24 août 2016;75(9):163-7.Rochat N, Olivier M, Chabli A, Conne F, Lefeuvre G, Boll-Burdet C. Multiple internal reflection infrared spectroscopy using two-prism coupling geometry: A convenient way for quantitative study of organic contamination on silicon wafers. Appl Phys Lett. 2 oct 2000;77(14):2249-51.Baum M, Rébiscoul D, Juranyi F, Rieutord F. Structural and Dynamical Properties of Water Confined in Highly Ordered Mesoporous Silica in the Presence of Electrolytes. J Phys Chem C. 30 août 2018;122(34):19857-68.Caër SL, Pin S, Esnouf S, Raffy Q, Ph. Renault J, Brubach JB, et al. A trapped water network in nanoporous material: the role of interfaces. Physical Chemistry Chemical Physics. 2011;13(39):17658-66.Davis KM, Tomozawa M. An infrared spectroscopic study of water-related species in silica glasses. Journal of Non-Crystalline Solids. 2 juin 1996;201(3):177-98. Figure 1

Radiative transfer model and validation for infrared management optical properties of porous polymer materials incorporating impacts of micro-voids

In order to characterize the infrared (IR) radiation absorption and/or emission performances of functional porous polymers which claim to have healthcare functions due to IR excitation and emission by processing technologies, a radiative transfer model was constructed based on the principle of IR radiation, the Beer–Lambert law, the Fresnel’s formula and Planck’s law. The theoretical analysis was conducted for the IR management optical properties of the porous sheet polymer materials, including IR reflection, transmission, absorption and emission behaviours during the dynamic process of IR radiation. A modeling method for characterization and revealing of IR management optical properties and optical and thermal transfer behaviours of the reflection and transmission was then investigated from the structural parameters and the temperature rise characteristics of the porous sheet polymer materials during the dynamic IR radiation process. The model was validated by comparing the predicted values from the radiative transfer model with the measured values from the test results of the validation experiments of eight typical porous sheet polymers in an experimental setup. The model was modified by consideration of the influences of two types of micro-voids defects represented by the porosity of micro structure and the thickness compression ratio. The micro-voids defects factors were added to the structural parameters, and therefore the model was improved and the maximum prediction errors of the transmission and reflection surfaces were mostly less than 10%. The radiative transfer model provides the theoretical fundamentals for the evaluation and guidance of IR management optical performances for new products design, development, fabrication and processing in industrial application of functional porous polymers.

Phonon Characteristics of Gas-Source Molecular Beam Epitaxy-Grown InAs1−xNx/InP (001) with Identification of Si, Mg and C Impurities in InAs and InN

The lattice dynamical properties of dilute InAs1−xNx/InP (001) epilayers (0 ≤ x ≤ 0.03) grown by gas-source molecular beam epitaxy were carefully studied experimentally and theoretically. A high-resolution Brüker IFS 120 v/S spectrometer was employed to measure the room-temperature infrared reflectivity (IRR) spectra at near-normal incidence (θi = 0). The results in the frequency range of 180–500 cm−1 revealed accurate values of the characteristic In-As-like and In-N-like vibrational modes. For InAs1−xNx alloys, a classical “Drude–Lorentz” model was constructed to obtain the dielectric functions ε~ω in the far IR regions by incorporating InAs-like and InN-like transverse optical ωTO modes. Longitudinal optical ωLO phonons were achieved from the imaginary parts of the simulated dielectric loss functions. The theoretical results of IRR spectra for InAs1−xNx/InP (001) epilayers using a multi-layer optics methodology provided a very good agreement with the experimental data. At oblique incidence (θi ≠ 0), our study of s- and p-polarized reflectance (Rs,p(ω)) and transmission (Ts,p(ω)) spectra allowed the simultaneous perception of the ωTO and ωLO phonons of the InAs, InN and InAs0.97N0.03 layers. Based on the average t-matrix Green’s function theory, the results of local vibrational modes for light SiIn+ donors and SiAs−, CAs− acceptors in InAs were found in good agreement with the existing Raman scattering and infrared spectroscopy data. InInN, however, the method predicted an in-band mode for the MgIn− acceptor while projecting an impurity mode of the SiIn+ donor to appear just above the maximum ωmaxInN[≡595 cm−1] phonon frequency region. In InAs1−xNx/InP (001) epifilms, the comparison of reflectivity/transmission spectra with experiments and the predictions of impurity modes for isoelectronic donor and acceptor impurities in InAs and InN can be valuable for appraising the role of defects in other technologically important semiconductors.

Infrared Spectroscopy Study of Edge Water Penetration at Hydrophilic Bonding Interface

In this article, we report on the use of a new characterization technique to measure the water penetration at the bonding interfaces and to quantify it. This complements previous studies done using X-ray reflectometry and surface acoustic microscopy: Fourier Transform Infra-Red Multiple Internal Reflection (FTIR-MIR) spectroscopy is used here to characterize the evolutions of contributions of silanols, surface bonded water and free liquid water groups.

The color rendering and near infrared reflection properties of coated iron oxide green pigments

In this study, a novel iron oxide green pigment (FePc), composed of phthalocyanine blue (CuPc) and iron oxide yellow pigments (FeOOH), was prepared by intermittent stirring. The FePc was coated with the hydrolysate of sodium metasilicate and silane coupling agent KH602. The structure and properties of prepared pigments were characterized by TEM, SEM, XRD, FT-IR, XPS, and TG-DTA techniques. The aspect ratio of FePc decreased compared to FeOOH. XPS analysis showed that CuPc and FeOOH were bound by hydrogen bonds. The thermal decomposition temperature of the coated pigments increased from 266 °C to 314 °C, and the color difference ΔE of pigment was 1.623 after baking at 240 °C for 30 min, indicating the prepared pigments had excellent heat resistance. The surface modification of FePc improved their hydrophobicity and dispersibility in organic media. The pigments with CuPc/FeOOH ratio of 0.2 exhibited well color properties (L* = 55.44, a* = −9.9, b* = 6.63), and green tone. The coating and surface modification had little impact on a* value. Particularly, all the newly prepared green pigments displayed high NIR reflectance. The prepared pigments have high heat resistance and dispersion properties, and are expected to be used in fields such as plastics and high-temperature coatings.

Facilitating methane conversion and hydrogen evolution on platinized gallium oxide photocatalyst through liquid-like water nanofilm formation

The dehydrogenative coupling of methane, an approach aimed at converting methane into valuable chemicals like ethane and hydrogen, can be facilitated under ambient thermal conditions using semiconductor photocatalysts. Herein, we present an efficient continuous-flow photocatalytic system for methane conversion by inducing the formation of physically adsorbed water nanofilms on the surface of a Pt-loaded Ga2O3 photocatalyst. The microscopic properties of the adsorbed water were examined by diffuse reflectance infrared (IR) spectroscopy and ab initio molecular dynamics (AIMD) calculations. In comparison to the photocatalytic non-oxidative coupling of methane operated in the absence of water vapor, the presence of the interfacial water resulted in a 90-fold and 500-fold enhancement in the production rate of hydrogen and ethane, respectively. The rate of ethane formation significantly increased with increasing water vapor pressure (PH2O) under a high methane pressure (PCH4) of 200 kPa. The selectivity for ethane reached 65 % based on carbon content at PH2O = 3 kPa and PCH4 = 200 kPa. Through diffuse reflectance IR spectroscopy, volumetric water vapor adsorption analysis, and AIMD calculations conducted under the reaction conditions, we observed the formation of a liquid-like water nanolayer on the Ga2O3 surface at 300 K. Thus, this strategy of inducing water nanofilms affords a highly efficient photocatalytic system for hydrogen and ethane production.

(Invited) Structure and Dynamics of Interfacial Species in Electrical Double Layer

Understanding electrochemical processes is of importance for many industrial and scientific fields. Especially, interfacial species, such as electrolyte ions and solvent significantly affect electrochemical reaction activity. Surface oxide species also promote or inhibit various electrode reactions; therefore, the oxidation processes of metal electrode have been investigated using in situ vibrational spectroscopy. Infrared (IR) spectroscopy is an important tool because it can detect the complementary vibrational modes of surface oxide species. However, observation of the low-frequency mode is restricted by infusible IR windows such as CaF2, that are generally used in the IR reflection absorption spectroscopy (IRAS). We developed a complementary IR method that can be used to avoid contamination by dissolved ions from window material. The fusible low-pass IR window can be applied to in-situ IRAS measurements [1,2]. The adsorbed hydroxide was observed on the single crystal Pt electrodes depending on the surface orientation, its coverage was correlated with the decrease in oxygen reduction reaction activity [3]. Recent time resolved X-ray diffraction measurements revealed that there is a delay in the approach of alkali metal cations to surface because the interfacial water causes a blocking effect [4]. Therefore, the kinetics of approaching step in the EDL is significantly different from that of migration in the bulk phase, and the adsorption rate depends on the hydration structure, ionic valence, and ionic size. Although X-ray diffraction provides a distribution of interfacial species, it does not provide sufficient information about species identification and molecular orientation. We investigated the coadsorption dynamics of metal cation and (bi)sulfate anion using time resolved IR measurement [5]. Boron doped diamond (BDD) is a promising material of which properties are significantly different from those of metals and other carbon materials. However, the complex atomic arrangement and oxidation state of the polycrystalline BDD surface inhibit an atomic level study on the relationship between the electrochemical response and surface structure. More detailed surface analyses are necessary for the investigation of the electrode surface of BDD. We applied in situ ATR−IR spectroscopy to reveal the oxidative species and dopamine oxidation on the BDD electrode [6,7].[1] M. Nakamura, Y. Nakajima, N. Hoshi, H. Tajiri, O. Sakata, ChemPhysChem, 14, 2426 (2013).[2] M. Nakamura, Y. Nakajima, K. Kato, O. Sakata, N. Hoshi, J. Phys. Chem. C, 119, 23586 (2015).[3] T. Kumeda, H. Tajiri, O. Sakata, N. Hoshi, M. Nakamura, Nat. Commun., 9, 4378 (2018).[4] M. Nakamura, H. Kaminaga, O. Endo, H. Tajiri, O. Sakata, N. Hoshi, J. Phys. Chem. C, 118, 22136 (2014).[5] M. Nakamura, T. Banzai, Y. Maehata, O. Endo, H. Tajiri. O. Sakata, N. Hoshi, Sci. Rep., 7, 914 (2017).[6] T. Ogose, S. Kasahara, N. Ikemiya, N. Hoshi, Y. Einaga, M. Nakamura, J. Phys. Chem. C, 122, 27456 (2018).[7] R. Hosoda, N. Kamoshida, N. Hoshi, Y. Einaga, M. Nakamura, Carbon, 171, 814 (2021).

Predicting the Surface Soil Texture of Cultivated Land via Hyperspectral Remote Sensing and Machine Learning: A Case Study in Jianghuai Hilly Area

Soil reflectance spectra and hyperspectral images have great potential to monitor and evaluate soil texture in large-scale scenarios. In hilly areas, sand, clay, and silt have similar spectral characteristics in visible, near-infrared, and short-wave infrared (VNIR-SWIR) reflection spectra. Soil texture spectra belong to mixed spectra despite some differences in particle size, mineral composition, and water content, making their distinction difficult. The accurate identification of the content within different particle sizes is difficult as it involves capturing spectral reflection features. Therefore, this study aimed to predict soil texture content through machine learning and unmixing the soil texture’s spectra while also comparing their respective modelling performances. Taking typical cultivated land in the Jianghuai hills as an example, the GaoFen-5 Advanced Hyperspectral Imaging (GF-5 AHSI) laboratory spectra of soil samples were used to predict sand, silt, and clay particle contents using partial least squares regression (PLSR) and convolutional neural networks (CNNs). The entire spectra of VNIR-SWIR regions were smoothed, and the dimensions were reduced via principal component analysis (PCA). The prediction models of sand, silt, and clay particle content were constructed, and inversion maps were generated using AHSI. The results showed that the PCA-CNN model achieved a higher prediction precision than the PCA-PLSR in both ASD and GF-5 data. Clay content exhibited the highest predictive performance with a coefficient of determination (R2) of 0.948 and 0.908 and a root mean square error (RMSE) of 26.51 g/kg and 31.24 g/kg, respectively, which represented a 39.0% and 79.8% increase in R2 and a 57% and 57.1% decrease in RMSE compared to that of the PCA-PLSR. This method indicates that the PCA-CNN model can effectively achieve nonlinear interactions between multiple spectral components and better model and fit spectral mixing processes; moreover, it provides an alternative method for investigating the spatial distribution of soil texture.

Multiprotein Adsorption from Human Serum at Gold and Oxidized Iron Surfaces Studied by Atomic Force Microscopy and Polarization-Modulation Infrared Reflection Absorption Spectroscopy.

Multiprotein adsorption from complex body fluids represents a highly important and complicated phenomenon in medicine. In this work, multiprotein adsorption from diluted human serum at gold and oxidized iron surfaces is investigated at different serum concentrations and pH values. Adsorption-induced changes in surface topography and the total amount of adsorbed proteins are quantified by atomic force microscopy (AFM) and polarization-modulation infrared reflection absorption spectroscopy (PM-IRRAS), respectively. For both surfaces, stronger protein adsorption is observed at pH 6 compared to pH 7 and pH 8. PM-IRRAS furthermore provides some qualitative insights into the pH-dependent alterations in the composition of the adsorbed multiprotein films. Changes in the amide II/amide I band area ratio and in particular side-chain IR absorption suggest that the increased adsorption at pH 6 is accompanied by a change in protein film composition. Presumably, this is mostly driven by the adsorption of human serum albumin, which at pH 6 adsorbs more readily and thereby replaces other proteins with lower surface affinities in the resulting multiprotein film.

Nanosized amorphous and nanocrystalline titania doped by Cr as novel, efficient, and cost-effective cool-colored nanopigments

Ceramic cool-colored nanopigments (NPGs) are becoming more promising in painting applications for their cooling and aesthetic performance. The phase structure and the doping by color elements play a crucial role in the performance of nanopigments. Throughout this study, pure titania (TiO2) and chromium (Cr)-doped TiO2 NPGs in nanosized amorphous and nanocrystals structures were synthesized using a simple hydrolysis route. The molar ratios of chromium (III) acetate hydroxide: titanium tetra isopropoxide are 0%, 5%, 15%, and 25%. The synthesized NPGs were studied as-synthesized and after annealing at 500oC and 700oC. X-ray diffraction analyses, FTIR and high-resolution transmission electron microscope (HRTEM) were utilized to explore the microstructure and property of the synthesized NPGs. Also, surface area of the synthesized NPG samples was estimated by BET measurement. Optical property of synthesized NPGs was specified by UV/Vis/NIR spectroscopy. The combined influences of the annealing temperature and Cr addition on the phase structure, grain growth and near infrared (NIR) reflectivity of NPGs have been investigated. Pure white TiO2 NPG annealed at 700oC was displayed the higher NIR solar reflectance (R* = 94.72%) than the other investigated NPGs. The presence of Cr ion in annealed TiO2 NPGs caused a massive reduction in R* which is reaching out to 21.5% for the highest Cr concentration with annealing at 700oC. While the NIR reflectivity of as-synthesized pure TiO2 was slightly reduced from 87.49% to 77.05% as Cr ion content was increasing. The reflectance parameter in the visible region (RVIS*) was determined for the studied NPGs to define their aesthetic performance. Moreover, the color coordinates CIE (L*, a* &b*) and (ho, C*) were presented for the investigated NPGs according to the perpendicular form and the polar form, respectively.

Operational Control of Substrates and Epitaxial Layers of Silicon Carbide and Diamond by IR Spectroscopy

A set of efficient operational methods for post-growth determination of the kinetic parameters of charge carriers and impurity concentration in silicon carbide and diamond substrates and epitaxial layers, as well as layer thicknesses, by analyzing infrared (IR) reflection and absorption spectra, is presented.

Synthesis and characterization of a high near infrared reflectance yellow pigment SbxWO3 (x ≤ 0.14)

In this work, a novel yellow near-infrared (NIR) reflective pigment based on the formula of SbxWO3 was developed by high temperature solid-state method at 700–900 °C. The formation of SbxWO3 was confirmed by XRD analysis, and the synthesized pigments are orthorhombic phase with high near infrared reflectivity (84.69%–87.28%). The acid/alkali resistance studies reveal that the color difference ΔE * of the pigments before and after soaking was less than 5, and the as prepared pigments are chemically stable under the atrocious weather. In addition, the synthetic pigments are bright yellowish green (L* = 92.1–92.9, a* = -4.9–4.1, b* = 35.0–37.0). In the heat insulation performance test, the indoor temperature with the SbxWO3 heat insulation coating is 3.1 °C lower than that without heat insulation coating. In summary, the as prepared SbxWO3 pigment has the advantages of high solar reflectivity and less toxic elements, making this new environmentally friendly energy-saving yellow pigment used as a colorant for building exterior coating formulations to reduce heat accumulation and cooling energy consumption.

Manipulation of ZrO2/CaZrO3 fibrous membrane with high thermal stability and NIR reflectivity

AbstractGrain size control is an important aspect to manipulate the microstructure and high temperature stability of ceramic fibers. In the present work, phase competition mechanism was proposed to regulate the grain size of ZrO2/CaZrO3 composite fibers. Calcium precursor with different molar ratio of Ca/Zr was introduced to the zirconia system not only for phase stabilization of ZrO2 but also for phase competition between solid‐solution CaxZr1‐xO2‐x and new phase CaZrO3. Effects of Ca/Zr molar ratio on the thermal pyrolysis, crystallization, solid reaction of precursor fibers were fully explored. The change of grain size of fibers with various Ca/Zr molar ratio was characterized and discussed. Furthermore, the near‐infrared reflectivity and high‐temperature stability of fibrous membranes were also presented. The results indicated that ZrO2/CaZrO3 fibrous membrane has promising applications in high‐temperature for the excellent thermal stability and high near infrared (NIR) reflectivity.

Microstructure FSS patterning to improve 5G microwave signals through low-e plastic windows

Low emissivity (low-e) windows are widely used in the architectural sector to block the infrared (IR) radiation from the Sun. The windows contain a multilayer nanoscale coating of metallic and dielectric layers. The metallic layer, which is responsible for the IR reflection, also attenuates the radio and microwave frequencies used for modern-day technologies such as Fifth Generation (5G) communications. As there is an ever-increasing demand for a reliable interior-to-exterior signal coverage, low-e windows should be transparent to such signals. A class of surface modification — Frequency Selective Surface (FSS) is the technique of choice to be applied on the thin metallic coating to transmit the wireless signal.In this work, a thin silver (Ag) film — 10 nm thick was deposited by electron beam evaporation on polycarbonate substrates as an example low-e coating. Despite excellent IR blocking (64 %) and visible light transmittance (60 %), it also presented a high attenuation of 20 dB at 5G signal bands (72–82 GHz).​ FSS patterns of various geometries and sizes were applied via laser ablation and evaluated to provide the lowest attenuation. We demonstrated that the application of the hexagonal pattern provided largest improvement reducing the 5G attenuation value from 20 dB to 1 dB, without compromising the visible transmittance and having only a minor effect on IR reflection.

New Insights into Cation- and Temperature-Driven Protein Adsorption to the Air–Water Interface through Infrared Reflection Studies of Bovine Serum Albumin

The chemistry and structure of the air-ocean interface modulate biogeochemical processes between the ocean and atmosphere and therefore impact sea spray aerosol properties, cloud and ice nucleation, and climate. Protein macromolecules are enriched in the sea surface microlayer and have complex adsorption properties due to the unique molecular balance of hydrophobicity and hydrophilicity. Additionally, interfacial adsorption properties of proteins are of interest as important inputs for ocean climate modeling. Bovine serum albumin is used here as a model protein to investigate the dynamic surface behavior of proteins under several variable conditions including solution ionic strength, temperature, and the presence of a stearic acid (C17COOH) monolayer at the air-water interface. Key vibrational modes of bovine serum albumin are examined via infrared reflectance-absorbance spectroscopy, a specular reflection method that ratios out the solution phase and highlights the aqueous surface to determine, at a molecular level, the surface structural changes and factors affecting adsorption to the solution surface. Amide band reflection absorption intensities reveal the extent of protein adsorption under each set of conditions. Studies reveal the nuanced behavior of protein adsorption impacted by ocean-relevant sodium concentrations. Moreover, protein adsorption is most strongly affected by the synergistic effects of divalent cations and increased temperature.

Dual-Function Smart Windows Using Polymer Stabilized Cholesteric Liquid Crystal Driven with Interdigitated Electrodes.

In this study, we present an electrically switchable window that can dynamically transmit both visible light and infrared (IR) light. The window is based on polymer stabilized cholesteric liquid crystals (PSCLCs), which are placed between a top plate electrode substrate and a bottom interdigitated electrode substrate. By applying a vertical alternating current electric field between the top and bottom substrates, the transmittance of the entire visible light can be adjusted. The cholesteric liquid crystals (CLC) texture will switch to a scattering focal conic state. The corresponding transmittance decreases from 90% to less than 15% in the whole visible region. The reflection bandwidth in the IR region can be tuned by applying an in-plane interdigital direct current (DC) electric field. The non-uniform distribution of the in-plane electric field will lead to helix pitch distortion of the CLC, resulting in a broadband reflection. The IR reflection bandwidth can be dynamically adjusted from 158 to 478 nm. The electric field strength can be varied to regulate both the transmittance in the visible range and the IR reflection bandwidth. After removing the electric field, both features can be restored to their initial states. This appealing feature of the window enables on-demand indoor light and heat management, making it a promising addition to the current smart windows available. This technology has considerable potential for practical applications in green buildings and automobiles.

Fabrication life prediction model for HDPE/Cr2O3 composites toward roof passive cooling

Passive cooling materials have been widely investigated to reduce building energy consumption. However, references about life prediction of the materials are insufficient. In this work, a novel life prediction model based on the passive cooling composites was established. The inorganic pigment chromium oxide (Cr2O3) was introduced into the high density polyethylene (HDPE) matrix to prepare HDPE/Cr2O3 composites with high long wave infrared (LWIR) emissivity and near infrared (NIR) reflectivity. The composites showed excellent cooling performance and color stability. The addition of ultraviolet absorber (UVA) and hindered amine light stabilizer (HALS) further improved the UV resistance of HDPE/Cr2O3 composites. HALS performs better and meets the needs of long-life outdoor use. Furthermore, a new failure point selection method is proposed and a model is established to predict the actual service life of HDPE/Cr2O3 composites, which provides theoretical guidance for the outdoor long-life use of the polymer composites. Based on the model, the fabricated HDPE/Cr2O3/HALS system can be used for more than 15 years. The long-term cooling composites can be used for building roof and wall to effectively reduce the indoor temperature and realize the sustainable use of energy. Besides, if used in military engineering, it has excellent cooling function and military camouflage effect. In addition, the composites can also be widely used in outdoor decoration, artificial lawn, floating materials and other fields.

Thermal performance analysis of near infra-red reflection and green roof cooling techniques on buildings made of mild steel

This paper investigates the thermal performance of green roofs, cool roofs, and their combined effects in tropical climates. Although each technology has been studied independently for its potential to reduce cooling energy consumption in buildings, their combined effects have not been thoroughly examined in tropical climates. The study employed experimental and numerical methods, demonstrating that combining green and cool roofs can lead to even greater cooling energy savings. The research involved fabricating four identical cubicles made of mild steel sheets and placing them in an open space for testing under two operational conditions: closed window and open window/door. The combined green and cool roof technology achieved a temperature difference reduction of 4.14 °C compared to the original roof under the closed window and door state, with green and cool roofs achieving 0.72 °C and 0.79 °C, respectively. Combining green and cool roofs led to even more significant cooling energy savings, with 53.57 kWh energy savings compared to 20.1 kWh and 3.68 kWh for combined, green, and cool cubicles, respectively. The study found that combining green and cool roofs led to even more significant cooling energy savings, with 53.57 kWh energy savings compared to 20.1 kWh and 3.68 kWh for combined, green, and cool cubicles, respectively. The research suggests that combining these technologies can lead to greater cooling energy savings and highlights the potential benefits of green and cool roofs for tropical climates.