UV Vis NIR Research Articles

Fabrication of chitosan coated bentonite clay multifunctional nanosorbents from waste biomass for the effective elimination of hazardous pollutants from waterbodies: A fixed bed biosorption, mechanism, and mathematical model study

The anthropogenic activity and hasty fluctuating technologies have been responsible for the generation of massive effluent which is so hazardous due to the loading of several toxicants. While most industries usually discharge it directly into the environment resulting in harsh damage to the ecology/public security. Therefore, it is critical to treat with a sustainable/cost-effective technique. Here, a new route of fabrication of chitosan-coated activated natural bentonite clay (CCANBC) bionanocomposites/bionanosorbents from waste biomass has been developed. Their potential application for the simultaneous removal of Ni2+ and Eosin Y from wastewater were investigated. The effective parameters like concentration (10–30 ppm), flow rate (2–4 mL/min), and bed height (0.5–1.5 cm) were inspected. The bionanosorbents were characterized by FTIR-ATR, XRD, FESEM, TGA, and BET analysis. Additionally, the effluents were explored by AAS and UV–vis-NIR spectroscopy. According to the findings it has been stated that the CCANBC bionanosorbents possessed significant dynamic edges, greater crystallinity (94.27 %), and higher thermal stability. They have exhibited a remarkable 2D honeycomb-like mesoporous microstructure with substantial specific surface area (19.29 m2/g). These outstanding features could be responsible for the dramatic adsorption enactment around 186.42 and 238.37 mg/g for Ni2+ and Eosin Y. The obtained data were evaluated by several mathematical models for better understanding the experimental BTC curve, reaction mechanism, and adsorption isotherm.

Microwave assisted synthesis of ErxYbyCa1-x-yMoO4 nano-phosphor for efficient temperature sensing and catalytic applications

Here, Er/Yb Co-doped CaMoO4 materials (ErxYbyCa1−x−yMoO4 NPs where x = 0, 0.01 and y = 0, 0.05, 0.10, 0.15, 0.20) were prepared by microwave-assisted method and its pure-tetragonal structure were confirmed by X-ray diffraction spectra (XRD), Rietveld-refinement and Raman-vibrational spectra. The transmission-electron microscopy (TEM) study indicates the formation of nearly spherical shaped nanomaterial with average size of ~ 15 nm. Additionally, absorption and emission properties were studied by UV–Visible–NIR and photoluminescence (PL) spectrometer. The UV–Visible–NIR spectra attribute absorption of Er3+ ion in visible region (380–700 nm) and absorption of Yb3+ ion in near-infrared region (700–1400 nm). Moreover, PL up-conversion spectra of the sample recorded under excitation wavelength 980 nm. The PL peaks were observed at 530, 544–552, and 656–670 nm. Prominent PL-intensity was observed for Er0.01Yb0.15Ca0.84MoO4 phosphor. Temperature dependent PL study reveals that present phosphor is robust phosphor for temperature sensor. In addition, Er3+/Yb3+ doped CaMoO4 nanomaterials exhibited excellent activity and selectivity in the aerial oxidation of benzoin over benzyl under oxidant-free reaction conditions. The synergistic effect Er3+/Yb3+ co-doing in CaMoO4 matrix was observed, where only CaMoO4 material found to be inactive towards above oxidation reaction. Moreover, the oxidation of primary benzyl-alcohols was furnished in presence of tertiary butyl hydroperoxideas oxidant.

The probing of local charge with sulfur encapsulated in single-walled carbon nanotubes

In this study, we demonstrated the remarkable sensitivity to electrochemical local charge of sulfur chains encapsulated in small-diameter single-walled carbon nanotubes (S@SWCNTs). To perform micro- and macro-spectroscopic probing, a transparent electrochemical cell was designed in which the charging electrode is formed based on S@SWCNTs. During a short-term electrochemical charging, significant reversible changes were observed in-situ in both Raman and UV–vis-Nir spectra of S@SWCNTs. The optical response was found to depend on the magnitude and sign of the charge, as well as on the duration of the electrochemical charging process at a given potential. The enhanced Raman modes of sulfur chains exhibited a notable linear shift (up to 10 cm-1) accompanied by a redistribution of their intensities. A correlation is identified of the chronoamperometry curve (charging current versus time) and transformations of the Raman spectrum of single-atom sulfur chains. Atomistic simulations allowed to attribute these changes in the Raman spectrum to the softening of the sulfur bonds upon charging. Our findings revealed that the nanotube inhibits the chemical interactions between encapsulated sulfur and local charge sources, thus rendering S@SWCNTs suitable for repeated utilization in local charge analysis.

Theoretical and experimental investigation of BaY2(MoO4)4:xSm3+ phosphors

In this paper, the novel BaY2(MoO4)4:xSm3+ phosphors with strong red emission and high thermal stabilization were prepared by a conventional method of high temperature solid state reaction in air atmosphere. Morphology, phase purity, element distribution, UV–Vis–NIR diffuse reflectance spectroscopy (DRS), and luminescence properties were investigated in detail. The crystal structure of the BaY2(MoO4)4 host was refined with the aid of the Rietveld refinement method by the GSAS program. The electronic band structure and phonon dispersion were performed using plane-wave density functional theory (DFT). The prepared BaY2(MoO4)4:Sm3+ phosphor exhibits excellent red emission under near-ultraviolet excitation. Strong red emission intensity and high thermal stability suggest potential application in backlighting or phosphor-covered white light-emitting diodes (pc-LEDs).

Effect of oxygen vacancies on enhancing the photo-catalytic activity, photo-luminescence and electronic structure properties of nanostructured Y-doped CeO2

The exceptional characteristics of CeO2 and Ce1-xYxO2 (x = 0.03, 0.05 and 0.07) nanoparticles were reported in the manuscript supporting that Y3+replaces Ce3+/Ce4+leads to oxygen vacancies formation. The results of XRD measurements revealed FCC structure of decreased crystallite size of CeO2 with improved crystallinity. To investigate the surface morphology, HRTEM and SAED patterns were performed. EDX analyses were undertaken to discuss the elemental and compositional characteristics. The absorption spectra using UV–Vis–NIR spectroscopy were analyzed and red shifted absorbance was found to enhance with decreasing band gap values for increased Y doping. The Photoluminescence spectra depicted various emissions representing the development of various defects and oxygen vacancy with incorporation of Y content in the lattice with CCT values below 4000 K to be classified as warm yellow light for indoor applications. The development of oxygen vacancies in the CeO2 lattice was further supported by XPS measurements for core levels Ce 3d, O 1s and Y 3d. Furthermore, the XPS measurements also reported the valence states of elements, Ce with 3+ and 4+, Y with 3+ and O with 2- along with charged oxygen vacancies. The photo-catalytic analysis revealed that Y-doped CeO2 nanoparticles show better degradation using a variety of characterization. A degradation mechanism that illustrates the impact of oxygen vacancies created by Y-doping on the photo-degradation process has been proposed. The novelty of Y-doped CeO2 nanoparticles stems from their improved photo-catalytic activities, which are linked to structural changes and the formation of oxygen vacancies. This doping considerably affects the electrical structure, resulting in better light absorption and less electron-hole recombination. The detailed outcomes of present study suggested the use of Y-doped CeO2 nanoparticles in optoelectronics, spintronics devices and photo-catalyst applications.

Magneto-optic properties of highly Dy3+-doped GeO2-B2O3 glasses for NIR optical applications

Recent progress in the development of optical communication and high power laser systems in the near-infrared (NIR) region (1.5 to 2.0 μm) increased the demand for magneto-optic (MO) devices employing MO materials. These MO materials are required with lower optical absorption coefficients and higher Verdet constants at spectral range of interest. In this study, two series of highly Dy3+-doped GeO2–B2O3 glasses with and without P2O5 were fabricated using a simple melt-quenching technique. The glasses were characterized through various techniques (Raman, UV–VIS-NIR, and DTA) for the evaluation of characteristic properties with respect to the Dy2O3 concentration and glass composition. Faraday rotation measurement was carried out at 1550 nm to quantify the Verdet constant of the glasses. The Verdet constant values were found to increase linearly with increasing Dy3+ concentration for both the glass systems. The increase in Dy3+ concentration and, consequently, the number of unpaired electrons, leads to an increase in the Verdet constant. The GeO2-B2O3 glass doped with 30 mol% of Dy2O3 exhibited the highest Verdet constant of −5.36 rad/(T⋅m) at 1550 nm. The glasses exhibited a good optical transparency (>70 %) in the region covering from 400 to 2400 nm. The thermo-physical, optical, and polarizability properties of both glass systems were also investigated. The results indicate that the highly Dy3+-doped glasses are attractive for magneto-optics at 1550 nm.

TiN/TiO2 embedded in ReS2 nanoflowers with wide light absorption and multi-interfacial charge transfer for efficient photocatalytic hydrogen generation

The design of functional materials with efficient light absorption and charge separation is crucial for photocatalytic energy conversion. Herein, a plasmonic TiN/TiO2/ReS2 ternary hybrid is prepared, which exhibits exceptional photocatalytic activity caused by the plasmon-mediated light absorption and multi-interfacial charge separation. The ternary hybrids were synthesized by heating TiN, Re, and S sources at high pressure and temperature. The TiN was partially oxidized to form TiN/TiO2 hybrids, which were then embedded in ReS2 nanoflowers through Ti-S bonds, creating a 3D flower-like structure with multiple interfaces. The plasmon resonance of TiN and the bandgap excitations of ReS2 and TiO2 endow the hybrids with efficient light absorption in UV–VIS-NIR region. Additionally, the novel embedded structure and the multiple interfaces between TiN, TiO2, and ReS2 facilitate the formation of built-in electric fields and multi-channel charge transfer, which efficiently quicken photoinduced carriers’ migration and hot electron injection. Consequently, the TiN/TiO2/ReS2 hybrids demonstrate a high-efficiency photocatalytic hydrogen generation rate, which is 12.1 times that of commercial P25. Notably, the hybrids also exhibit high photocatalytic activity under near-infrared light irradiation. This study offers innovative insights into the design of photocatalysts and suggests that the prepared materials could be utilized in solar-driven energy conversion applications.

Low-temperature flux synthesis of potassium hexatitanate whiskers: Growth mechanism and applications in high-temperature infrared thermal insulation

Potassium hexatitanate whiskers (PHWs, K2Ti6O13)are a promising functional material with high thermal insulation capacity. In this study, PHWs were successfully synthesized using the flux method at temperatures ranging from 725 °C to 1100 °C. The crystal growth mechanism of PHWs in the KCl flux follows a series-parallel pattern. The synthesized PHWs have a near-infrared reflectivity (NIR) exceeding 95%, and the cause of high reflectivity was theoretically analyzed based on the Kubelka-Munk equation. The high temperature stability of near-infrared reflectivity and the thermal stability of the PHWs were further assessed using TG-DSC, XRD, SEM, and UV–VIS-NIR analysis. It was found that PHWs prepared at 800 °C begin to decompose into TiO2 at approximately 1375 °C. Nevertheless, the near-infrared reflectivity remains stable even after heat treatment. Additionally, PHWs were prepared as a composite thermal insulating coating, showing thermal conductivity between 0.177 and 0.569 W/(m K) across the temperature range of 200 °C to 900 °C. The temperature difference between the hot and cold surfaces of the composite coating was significantly greater compared to the control groups at various temperatures, with a p-value of less than 0.01 in the paired t-test. This result demonstrates the great application potential of PHWs as a high-temperature near-infrared thermal insulation material.

Single layered Ag/NiO plasmonic nanocoatings: A new green synthesis method for selective solar absorber

This study presents the synthesis of environmentally benign, single-layered spectrally selective Ag/NiO nanocoating absorbers using a green synthesis method. Various characterization techniques, including Rutherford backscattering spectroscopy (RBS), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM), were used to examine the effects of plasmonic Ag concentration on the structural, chemical composition, and surface morphology of the nanocomposites. The optical properties of the deposited nanocoatings were investigated using a UV–Vis-NIR spectrophotometer in the solar spectrum region (300–2500 nm) and an FT-IR spectrophotometer in the infrared wavelength region (3000–20,000 nm). XRD results confirmed the coexistence of a face-centered cubic phase of Ag and NiO in the Ag/NiO nanocermet thin films. SEM and TEM topography revealed uniformly distributed nanosphere NiO thin films and cubic Ag metal with better dispersibility and crystallization. The RBS spectrum of the samples showed a homogeneous distribution of Ni, Ag, and O atoms throughout the coatings. Ag/NiO nanocoatings deposited with 8 wt% Ag content exhibited excellent solar absorptance (α) = 0.95 and thermal emittance of (ɛ) of 0.08. This enhancement is primarily attributed to the localized surface plasmon resonance (LSPR) effect associated with the embedded Ag nanoparticles, which facilitates more effective utilization of light.

Synthesis, structure and characterizations of the first alkali-metal/alkaline-earth-metal oxalatophosphate Na4Mg3(HPO4)4(C2O4)·2H2O

The first alkali-metal/alkaline-earth-metal oxalatophosphate Na4Mg3(HPO4)4(C2O4)·2H2O with monoclinic P21/n space group was successfully synthesized by a conventional solvothermal method. Na4Mg3(HPO4)4(C2O4)·2H2O crystal exhibits a typical three-dimensional structure built by isolated [C2O4] and [HPO4] anionic groups connected by Na and Mg atoms. The HPO42− groups are linked by hydrogen bonds to form an unique one-dimensional zigzag band ∞[HPO4]2-, which exhibits a stable “Mortise-Tenon” structure configuration within the bc plane. Fourier transform infrared (FTIR) spectrum and Raman spectrum confirm the crystal structure of Na4Mg3(HPO4)4(C2O4)·2H2O. UV–visible near infrared (UV–Vis–NIR) diffuse reflectance and band structure calculation indicate that Na4Mg3(HPO4)4(C2O4)·2H2O is an indirect bandgap semiconductor with a bandgap of 4.42 eV. In addition, Na4Mg3(HPO4)4(C2O4)·2H2O shows a moderate birefringence of 0.046 at 550 nm.

Revealing the complexation of 3-N,N-dimethylaminodithiocarbamoyl-1-propanesulfonic acid (DPS) with cuprous ion and its contribution to Cu electrodeposition

An accelerator is an organic additive used in Cu electrodeposition, crucial for achieving superfilling during the fabrication of Cu interconnects in microelectronics. 3-N,N-dimethylaminodithiocarbamoyl-1-propanesulfonic acid (DPS) has been proposed and investigated as a substitute for SPS. However, its acceleration mechanism associated with its interaction with Cu ions has not been intensively investigated. In this study, the interaction between DPS and Cu+ was investigated using various spectroscopic analyses, including ultraviolet–visible–near-infrared absorption (UV–VIS–NIR), electron paramagnetic resonance (EPR), and nuclear magnetic resonance (NMR) spectroscopy. UV–VIS–NIR and EPR spectroscopy revealed that DPS forms a complex with Cu+, namely Cu(I)(DPS)2. The kinetic study on the complexation of DPS with Cu+ indicated second-order reaction characteristics. The structure of the complex was suggested using 1H and 13C NMR spectroscopy. Furthermore, electrochemical analyses, including cyclic voltammetry (CV) and linear sweep voltammetry (LSV), were conducted to investigate the electrochemical behaviors of the Cu(I)(DPS)2 complex, demonstrating its acceleration effect on Cu electrodeposition. These results will provide valuable insights for understanding the acceleration mechanism of DPS in Cu electrodeposition.

The impact of proton ion irradiation on Se70Te20In10 thin films: Linear and non-linear optical properties for photonic applications

The examination of the linear and non-linear optical features was conducted on amorphous ternary Se70Te20 In10 thin films, which were exposed to proton irradiation energy of 3 MeV at varying fluences of 5×1013, 5×1014, 5×1015 and 5×1016 ions/cm2. The bulk sample was produced using the melt quenching method, and subsequently, thin films were obtained through electron beam evaporation. Calculations of linear and non-linear optical parameters were carried out based on transmittance and reflectance data acquired from UV–Vis–NIR spectroscopy spanning 300–2500 nm. Field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD) confirmed an amorphous phase in the films. The optical parameters showed strong dependency on the proton radiation fluence. In addition, the existence of minima or maxima for a number of parameters at a fluence of 5×1014 ions/cm2 showed that this was the optimum fluence. The linear and non-linear properties showed that the sample have potential applications in photonic devices.

Tailoring the Structural and Optical Properties of Oxychloride Magnesium Tellurite Glass with the Addition of Samarium Ions

In this study, samarium-doped oxychloride magnesium tellurite glass with composition (79−x)TeO2−xMgO−20Li2O−1Sm2O3 (Series 1) and (79−x)TeO2xMgCl2−20Li2O−1Sm2O3 (Series 2) with 0 ≤ x ≤ 15 mol% was prepared by the melt-quenching technique. The structural and optical properties of synthesized samples were investigated, and the XRD results dictated an amorphous nature for both samples. The glass density of both Series 1 and 2 decreased with increasing MgO and MgCl2 content. However, the molar volume behaves in a completely opposite manner to an increase in MgO or MgCl2 content. FTIR spectra revealed from the vibrational wavenumber shift of TeO4 and TeO3 structural units showed a significant rise in HOH vibration mode, which implies its usefulness in boosting water and light absorption. Four absorbance bands were observed via UV-Vis NIR, while the indirect optical band gap around (3.42–3.36) eV and (3.42−3.30) eV for Series 1 and Series 2 were observed from UV-Vis spectroscopy. The emission spectra from the photoluminescence study revealed four distinct bands centered at 562.54, 599.14, 645.63 and 708.40 nm which are attributed to the transition from 4G5/2 – 6HJ/2 (J = 5,7,9,11) of states of Sm3+. The optimum glass with a composition of TeO-MgO 15% demonstrates a high potential for optical device development.

Stoichiometric effect on the defect states and optical properties of LiInSe2 single crystals

LiInSe2 crystals are promising semiconductor materials for neutron detectors due to the large neutron capture cross-sectional area of the specific isotopes (6Li) and high charge transport properties. However, the optoelectronic performance fails to reach the expected level due to the difficulty of controlling the crystal defects. Herein, we modulate the stoichiometric ratio to control the type of defects in single LiInSe2 crystals grown by the vertical Bridgman method. The UV‒vis–NIR transmission results indicate that the band gap of the yellow colored Li1.01In1Se2 sample is close to ~ 2.83 eV at room temperature, and this value is consistent with the theoretical band gap of LiInSe2 (~ 2.86 eV). Photoluminescence (PL) spectroscopy was used to analyze the defect concentration. The results indicate that the defect types in the yellow Li1.01In1Se2 single crystal are VSe+ and LiIn2−; these result from the introduction of excess Li and the suppression of the adverse defects in InLi2+ and VLi−. These results demonstrate a feasible route for obtaining high-quality yellow 6LiInSe2 crystals and promote the application of 6LiInSe2 neutron detectors.

Superparamagnetic iron oxide nanoparticles functionalized with on-demand redox-responsive contractible coordination polymer brush as molecular actuator driven by π-dimerization

Nanomachines require molecular actuators to be coupled to a condensed phase. In this work, a redox responsive 1D contractible coordination polymer (ZnL) used as non-interlocked actuator is grafted onto superparamagnetic iron oxide nanoparticles (SPIONs) in a brush-like configuration. Oxidized rod-like ZnL oligomers have ability to reversibly self-fold upon reduction via π-dimerization of their bis-viologen units. Unlike in usual responsive brushes, ZnL chains behave individually, generating spatially controlled mechanical motion at nanoparticle surface associated to significant variations of particle diameters. ZnL oligomers were “grafted to” SPIONs in a single step. Reduction of colloidal dispersions was perform by visible light illumination with the help of a photoreductant. π-dimerization was assessed by UV–vis–NIR and reversible contraction of ZnL brush was characterized by DLS. Effects of ZnL chains length and grafting density on mechanism and performance of contractibility were studied. ZnL brush can alternately be contracted and extended with excellent reversibility. Combined UV–vis–NIR, DLS and TGA analyses demonstrate that π-dimerization is only intramolecular and that chains behave as independent actuators. Maximal contraction of 22 nm is obtained for largest particles (DH = 86 nm). Full to partial contraction of the brush depends on grafting density with a threshold at ≈ 47 chains per particle.

Crystal growth, linear optical, thermal, mechanical and third-order nonlinear optical properties of 1,3-diphenyl prop‑2-en-1-one single crystals

This work brings out the viability of the chalcone derivative (E)-1,3-diphenyl-2-propen-1-one (DPP) for industrial applications in nonlinear optical technology and device fabrication, through investigations on its crystal structure and nonlinear optical properties. The unit cell features of the DPP single crystals grown by slow evaporation solution growth method have been determined and hkl values indexed. The optical transparency of DPP in the near infrared and visible range is found to be admirable and an optical bandgap of 3.42 eV is revealed in the UV–Vis-NIR analysis. The work hardening coefficient (n) of DPP, determined as 2 from Vickers microhardness measurement, shows the moderate mechanical strength of the crystal. The Laser Damage Threshold value of 3.9 GW/cm2 sheds light on the high tolerance of DPP to optical damage and suggests its suitability in device fabrication. The potential of DPP crystal in nonlinear optical applications is suggested from its superior value of 1.16×10−7 esu for third order susceptibility and appealing values of other nonlinear optical parameters.

Elucidating temperature-dependent local structure change and optical properties in GeTe phase-change material

Phase-change memory emerges as a top contender for non-volatile data storage applications. We report here a systematic change in local structure and crystallization kinetics of binary GeTe thin films using temperature-dependent resistivity measurements, which offers single-stage crystallization at around 187 °C, corroborated with x-ray diffraction. Furthermore, the change in chemical bonding upon crystallization is determined through x-ray photoelectron spectroscopy core level spectra, which reveals the existence of Ge and Te components that align with the GeTe crystal structure. Also, an investigation was carried out employing a UV–Vis–NIR spectrophotometer to explore the evolution of optical bandgaps (Eg), Tauc parameter (B) representing the local disorder, and Urbach energy (Eu) of the GeTe material, as it undergoes the transition from a disordered amorphous state to a crystalline state. As crystallization progresses, a consistent shift of Eg from 0.92 to 0.70 eV corresponds to as-deposited amorphous at room temperature and crystalline at 250 °C, respectively. In addition, the reduction in Eu (from 199.87 to 141.27 meV) and a sudden increase of B around crystallization temperature is observed upon increasing temperature, indicating direct observation of enhanced medium-range order and distortion in short-range order, respectively, in GeTe thin films, revealing improved structural and optical properties. These enhancements make the GeTe material ideal for data storage applications of phase-change memory for next-generation computing technology.

Investigation of annealing temperature effect on structural, morphological, optical, magnetic, and dielectric properties of cobalt-doped manganese ferrites

Spinel ferrite Mn0.95Co0.05Fe2O4 was prepared via chemical co-precipitation routes and annealed at four distinct temperatures of 600 °C, 650 °C, 700 °C, and 750 °C. The XRD peak confirmed a single-phase cubic spinel structure, with an increasing crystallite size of 21.64–23.98 nm by the annealing effect. The TEM images show an increase in particle size with rising annealing temperature and indicate well-defined nanocrystalline Mn-Co ferrite. FT-IR spectra detected two vibrational modes at interstitial sub-lattice sites, identifying Co-O, Mn-O, and Fe-O bonds with the spinel structure of Mn-Co ferrite. UV–vis–NIR reflectance revealed an optimal direct band gap of 3.76–4.70 eV, indicating a scope of semiconducting behaviors in the nanocatalysts. In the magnetic hysteresis curve, saturation magnetization decreased while coercivity increased with rising annealing and crystallite size. The M-T loop reveals the Curie temperature of Mn-Co ferrite decreases from 533.84 °C to 382.74 °C. Frequency-dependent complex permeability at different annealing temperatures shows stable initial permeability over a wide frequency range (1 kHz to 100 MHz) and a quality factor several times higher due to reduced magnetic tangent loss. The real dielectric constant and losses decline in rising alternating fields (100 Hz to 1 MHz) and stabilize at higher frequencies following Maxwell-Wagner-type polarization. Eventually, structural, morphological, and magnetic properties are performed relatively well at higher annealing temperatures, and optical and dielectric properties are performed at lower annealing temperatures.

Improving broadband absorption of carbon dot conjugated melanin via pre-doping strategy as interfacial photothermal evaporator

Photothermal seawater desalination harnesses solar energy to induce heat and expediates seawater evaporation and purification. The desalination efficacy heavily relies on the light absorption capability and microstructure of the solar evaporator. Polydopamine (PDA) represents a typical synthetic melanin with broad spectral absorption characteristics. However, its absorption capacity within the near-infrared (NIR) region is limited, leading to inadequate photothermal conversion efficiency. To overcome this challenge, we adopt a straightforward approach involving the pre-doping of N,S-doped carbon quantum dots (N,S-CQDs) with dopamine through covalent interaction to fabricate CQDs-loaded mesoporous polydopamine (MPDA-8). This strategy effectively reduces the band gap of PDA by fostering additional donor–acceptor pairs and π-stacking structures, thereby broadening the absorption capacity across the UV–Vis-NIR spectrum through nonradiative transitions. The MPDA-8 coated Balsa wood and cellulose evaporator achieved high evaporation rates of 1.82 kg m−2 h−1 and 2.10 kg m−2 h−1, respectively, overcoming the limit of 2D interfacial evaporator. The small pores and fiber channels within the wood, coupled with the hydrophilicity of MPDA-8, facilitates efficient water transportation and reduces evaporation enthalpy. Outdoor evaporation experiments conducted under sunlight corroborated the practical viability of this material. This study introduces a new perspective for advancing synthetic melanins in photothermal applications through the nanoparticle pre-doping strategy.

Thin film synthesis and photovoltaic performance of polypyrrole@cobalt hydroxide composites for solar cells and optoelectronic devices

Mono-nanocomposites (MNCs) comprising polypyrrole (PPy) and cobalt hydroxide nanoparticles (Co(OH)2 NPs) are emerging as highly favorable contenders for applications in solar cells and optoelectronic devices, owing to their distinctive attributes encompassing robust light absorption, elevated conductivity, and commendable chemical stability. This investigation delves into the production of a thin film [PPy@Co(OH)2]MNC utilizing the physical vapor deposition (PVD) method. The structural and morphological characteristics of the [PPy@Co(OH)2]MNC thin film were scrutinized through X-ray diffraction (XRD) and scanning electron microscopy (SEM). Optical properties, namely reflectance (R), absorbance (Abs), and transmittance (T) within the UV–vis–NIR spectrum, were precisely gauged at room temperature. Time-dependent density functional theory (TD-DFT) calculations and optimizations were conducted to analyze the geometric parameters, while the refractive index dispersion was probed using the single oscillator Wemple-Didomenico (WD) model. Additionally, the energy of a single oscillator and the energy of dispersion were quantified. The [PPy@Co(OH)2]MNC thin film exhibited pronounced light absorption across the UV–vis–NIR spectrum, characterized by a bandgap of 1.6 eV. The Au/[PPy@Co(OH)2]MNC/p-Si/Al heterojunction device demonstrated a power conversion efficiency and fill factor (FF) of 2.6 % and 55.07 %, respectively, under an irradiance of 100 W/cm2. The findings of this investigation underscore the potential of [PPy@Co(OH)2]MNC-based thin films as auspicious candidates for deployment in solar cells and optoelectronic devices.