Maximum Absorption Research Articles

Plasmonic metamaterial absorber for MWIR and LWIR bispectral microbolometers

Plasmonic metamaterial absorbers (PMAs) designed for multispectral imaging in the infrared (IR) with uncooled microbolometers are investigated. The study presents Fourier transform infrared spectroscopy (FTIR) measurements of PMAs consisting of metal-insulator-metal-stacks (MIM) with square-shaped micropatches as top metal layers. The measurements reveal high absorptances of 82% to 99% for distinct wavelengths within a range from 2 μm to 9.2 μm. The spectra are evaluated with respect to the lateral dimensions of the patches and to the refractive indices of the used dielectrics SiO2, Al2O3 and Ta2O5. Numerical simulations and analytical calculations of the TM010-mode using the transmission line model (TLM) for microstrip antennas show good qualitative agreement with the measurement results. Additionally, bispectral PMAs were fabricated consisting of fields of PMAs with two different patch sizes arranged in a chessboard pattern. The individual fields of this pattern correspond to microbolometers with 12 μm pitch in shape and size. Two distinct absorption maxima can be seen in the spectra measured by FTIR. The choice of materials, deposition methods and patterning processes is suitable for the integration into the existing Fraunhofer IMS's nanotube microbolometer technology to realize multispectral infrared imaging. The fabrication process is CMOS-compatible and carried out on 8-in. wafers.

On the Durability Performance of Two Adhesives to Be Used in Bonded Secondary Structures for Offshore Wind Installations.

The development of offshore wind farms requires robust bonding solutions that can withstand harsh marine conditions for the easy integration of secondary structures. This paper investigates the durability performance of two adhesives: Sikadur 30 epoxy resin and Loctite UK 1351 B25 urethane-based adhesive for use in offshore wind environments. Tensile tests on adhesive samples and accelerated aging tests were carried out under a variety of temperatures and environmental conditions, including both dry and wet conditions. The long-term effects of aging on adhesive integrity are investigated by simulating the operational life of offshore installations. The evolution of mechanical properties, studied under accelerated aging conditions, provides an important indication of the longevity of structures under normal conditions. The results show significant differences in performance between the two adhesives, highlighting their suitability for specific operating parameters. It should also be noted that for both adhesives, their exposure to different environments (seawater, distilled water, humid climate) over a prolonged period showed that (i) Loctite adhesive has a slightly faster initial uptake than Sikadur adhesive, but the latter reaches an asymptotic plateau with a lower maximum absorption rate than Loctite adhesive; and (ii) a progressive deterioration in the tensile properties occurred following an exponential function. Therefore, aging behavior results showed a clear correlation with the Arrhenius law, providing a predictive tool for the aging process and the aging process of the two adhesives followed Arrhenius kinetics. Ultimately, the knowledge gained from this study is intended to inform best practice in the use of adhesives, thereby improving the reliability and sustainability of the offshore renewable energy infrastructure.

Theoretical Insights into the Structural and Optical Properties of D-π-A-based Cyanostilbene Systems of α and β Variants.

The π-conjugated organic molecules containing cyanostilbene motifs have been extensively investigated due to their great potential applications in several optoelectronic and biological fields. Developing efficient molecules in this respect requires strategic structural engineering and a deep understanding of the structure-property relationship at the molecular level. In this context, understanding the impact of positional isomerism in cyanostilbene systems is a fundamental aspect of designing desired materials with improved photophysical properties. Herein, we designed ten donor-π-acceptor (D-π-A) type cyanostilbene derivatives (P1 - P10) with different π linkers and compared their structural and optoelectronic properties arising from the positional variations of the -CN group (α and β- variations) through the utilization of density functional theory (DFT) and time-dependent DFT (TDDFT) methods. The topological analyses of the electron density are used to explain the relatively high stability of α isomer compared to that of β. Frontier molecular orbital analysis reveals that 17 molecules tend to show a reduced highest occupied molecular orbital-lowest unoccupied molecular orbital gap, and most of them showed a greater nonlinear optical (NLO) character compared to the parent molecule. TDDFT calculations indicate that β isomers show higher absorption maxima compared to their α counterparts. Among all the scrutinized molecules, the absorption maximum extended up to 602 nm for P9 and it possesses the highest first-order hyperpolarizability. This study sheds light on positional isomers and their reactivity, absorption spectra, and NLO properties of D-π-A type architecture that can be suitably tuned by appropriating the π-bridge for practical applications.

The role of secondary donor in thiophene-based azo dyes for dye-sensitized solar cells and non-linear optics

The effect of altering the donating strength of secondary donors at the 4th position of the thiophene ring in a series of dyes labeled AB1 to AB9 is investigated in this study. According to the findings, the orientation of the secondary donor has a considerable impact on molecular planarity, resulting in changes in charge transfer (CT) properties within the thiophene-azo-benzoic acid backbone. The time-dependent density functional theory (TD-DFT) study supports these findings, indicating that the vertical absorption maximum of the dyes increases with the secondary donor's donating strength. From AB1 to AB5, photovoltaic parameters show an increase in DSSC performance. Furthermore, dye@TiO2 cluster experiments suggest the possibility of these dyes interacting with TiO2, resulting in red-shifted absorbance of dye@TiO2 clusters.Theoretical predictions are confirmed by the synthesis of AB1 to AB4, with initial absorption in dimethylformamide (DMF) and energies of highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) following a similar pattern as observed in density functional theory (DFT) studies. TGA results show that AB1 to AB4 have remarkable thermal stability, enabling their practical application in DSSCs. The efficiencies of the constructed DSSCs varied, with AB4 having the highest (1.90 ± 0.1) and AB1 having the lowest (1.29 ± 0.1). Secondary donors play a critical role in determining molecular characteristics and device performance, according to the theoretical and experimental DSSC results.

Formulation and Evaluation of Betulin Loaded Transdermal Patches

Objectives: To develop and evaluate Transdermal patches of Betulin along with various polymers for controlled release action. Method: Suitable method such as Solvent Casting Technique of Film Casting Technique are used for preparation of Transdermal patch. Result: The prepared Transdermal patches were transparent, smooth, uniform and flexible. The method adopted for preparation of system was found satisfactory. Conclusion: Various formulations were developed by using hydrophilic and hydrophobic polymers like HPMC E5 and EC respectively in single and combinations by solvent evaporation technique with incorporation of penetration enhancer such as dimethylsulfoxide and dibutyl phthalate as plasticizer. Formulation F7 containing equal ratio of HPMC E5: EC (5:5) showed maximum percentage drug content 95.44%. A suitable UV Spectroscopy method for the analysis of Betulin was developed. Betulin showed maximum absorption at wave length 215 nm in isotonic phosphate buffer (pH 7.4) solutions. The pre-formulation studies involving description, solubility, melting point, partition coefficient of the drug were found to be comparable with the standard. The Transdermal patch of Betulin was prepared successfully by solvent evaporation method. Transdermal patch of Betulin for Transdermal drug delivery was evaluated. Calibration curve was obtained; Transdermal film was prepared, overcome limitations regarding bioavailability of drug was done. Keywords: Controlled DDS, Transdermal DDS, Betulin, Transdermal Patch, solvent evaporation method.

Amorphous/Graphitic carbon phase engineering of Corrosion-Resistant Fe@C Core-Shell nanowires for optimized dipole polarization and enhanced microwave absorption

The study of designing and developing ferromagnetic nanocomposites with both microwave absorption (MA) and corrosion protection properties through microscopic heterogeneous interfacial engineering and crystal phase engineering remains challenging. In this study, Fe@C core–shell nanowires (FCNWs) are obtained by magnetic field-controlled in situ reduction method and annealing process to de-regulate the carbon shell thickness and carbon morphology. The enhancement of Fe-C heterogeneous relative interfacial effects and dielectric/magnetic response is revealed using density functional theory and simulated electromagnetic field distribution, and the modulation of the amorphous carbon/graphitic carbon ratio achieves the enhancement of dipole polarization in the low-frequency region. The FCNWs absorber had a minimum reflection loss (RLmin) of −47.6 dB at a thickness of 4.9 mm, and the maximum effective absorption bandwidth (EABmax) was achieved at 5.5 mm up to 4.0 GHz. In addition, the shielding effect of the graphitic carbon shell on the corrosion medium and the addition of additional electron conduction pathways allow the FCNWs absorber to obtain smaller corrosion currents and larger polarization resistances compared to Fe nanowires. Thus, modulation of atomic-scale heterogeneous interfaces and crystal phases has great potential in modulating the dielectric response.

Exploring of Be1-xCrxSe alloys for spintronics and optoelectronic applications

In this study, spin polarized density functional theory (DFT) is implemented to predict physical characteristic of Be1-xCrxSe (x = 6.25%, 12.5%, 18.75%, 25%) compound. The electronic characteristics of pure BeSe compound show semiconductor behavior but after Cr doping BeSe elucidate half-metallic ferromagnetism (HMF) for all doping concentrations. The outcomes elucidate the total magnetic moment MTot per Cr-atom are 4.0028, 4.0027, 4.0021 and 4.0002 μB for 6.25%, 12.5%, 18.75%, 25% concentrations, respectively and the magnetism mainly originated from d-state of the impurity atom which is further ensured from the magnetic spin density. Furthermore, the optical parameters are also computed to determine the effect of doping on the material’s response to incident light of energy spanning from 0 to 10 eV. The optical study depict that the studied systems possess maximum absorbance and optical conductivity in UV-range with minimal reflection. The overall outcomes illustrate that the Cr doped beryllium selenide (BeSe) is promising material for spintronic and optoelectronic devices.

Boost the Circularly Polarized Phosphorescence of Chiral Organometallic Platinum Complexes by Hierarchical Assembly into Fibrillar Networks.

Circularly polarized luminescence (CPL)-active molecular materials have drawn increasing attention due to their promising applications for next-generation display and optoelectronic technologies. Currently, it is challenging to obtain CPL materials with both large luminescence dissymmetry factor (glum) and high quantum yield (Φ). A pair of enantiomeric N N C-type Pt(II) complexes (L/D)-1 modified with chiral Leucine methyl ester are presented herein. Though the solutions of these complexes are CPL-inactive, the spin-coated thin films of (L/D)-1 exhibit giantly-amplified circularly polarized phosphorescences with |glum| of 0.53 at 560 nm and Φair of ~50 %, as well as appealing circular dichroism (CD) signals with the maximum absorption dissymmetry factor |gabs| of 0.37-0.43 at 480 nm. This superior CPL performance benefits from the hierarchical formation of crystalline fibrillar networks upon spin coating. Comparative studies of another pair of chiral Pt(II) complexes (L/D)-2 with a symmetric N C N coordination mode suggest that the asymmetric N N C coordination of (L/D)-1 are favorable for the efficient exciton delocalization to amplify the CPL performance. Optical applications of the thin films of (L/D)-1 in CPL-contrast imaging and inducing CP light generation from achiral emitters and common light-emitting diode lamps have been successfully realized.

Boost the Circularly Polarized Phosphorescence of Chiral Organometallic Platinum Complexes by Hierarchical Assembly into Fibrillar Networks

AbstractCircularly polarized luminescence (CPL)‐active molecular materials have drawn increasing attention due to their promising applications for next‐generation display and optoelectronic technologies. Currently, it is challenging to obtain CPL materials with both large luminescence dissymmetry factor (glum) and high quantum yield (Φ). A pair of enantiomeric N N C‐type Pt(II) complexes (L/D)‐1 modified with chiral Leucine methyl ester are presented herein. Though the solutions of these complexes are CPL‐inactive, the spin‐coated thin films of (L/D)‐1 exhibit giantly‐amplified circularly polarized phosphorescences with |glum| of 0.53 at 560 nm and Φair of ~50 %, as well as appealing circular dichroism (CD) signals with the maximum absorption dissymmetry factor |gabs| of 0.37–0.43 at 480 nm. This superior CPL performance benefits from the hierarchical formation of crystalline fibrillar networks upon spin coating. Comparative studies of another pair of chiral Pt(II) complexes (L/D)‐2 with a symmetric N C N coordination mode suggest that the asymmetric N N C coordination of (L/D)‐1 are favorable for the efficient exciton delocalization to amplify the CPL performance. Optical applications of the thin films of (L/D)‐1 in CPL‐contrast imaging and inducing CP light generation from achiral emitters and common light‐emitting diode lamps have been successfully realized.

Design and preparation of reticular superabsorbent hydrogel material with nutrient slow-release and high shear strength for ecological remediation of abandoned mines with steep slopes

In order to solve ecological remediation issues for abandoned mines with steep slopes, a kind of hydrogels with high cohesion and water-retaining were designed by inorganic mineral skeleton combining with polymeric organic network cavities. This eco-friendly hydrogel (MFA/HA-g-p(AA-co-AM)) was prepared with acrylic acid (AA)-acrylamide (AM) as network, which was grafted with humic acids (HA) as network binding point reinforcement skeleton and polar functional group donors, KOH-modified fly ash (MFA) as internal supporter. The maximum water absorption capacities were 1960 g/g for distilled water, which followed the pseudo-second-order model. This super water absorption was attributed to the first stage of 62 % fast absorption due to the high specific surface area, pore volume and low osmotic pressure, moreover, the multiple hydrophilic functional groups and network structure swell contributed to 36 % of the second stage slow adsorption. In addition, the pore filling of water in mesoporous channels contributed the additional 2 % water retention on the third stage. The high saline-alkali resistance correlated with the electrostatic attraction with MFA and multiple interactions with oxygen-containing functional groups in organic components. MFA and HA also enhanced the shear strength and fertility retention properties. After 5 cycles of natural dehydration and reabsorption process, these excellent characteristics of reusability and water absorption capacity kept above 97 %. The application of 0.6 wt% MFA/HA-g-p(AA-co-AM) at 15° slope could improve the growth of ryegrass by approximately 45 %. This study provides an efficient and economic superabsorbent material for ecological restoration of abandoned mines with steep slopes.

Ruthenium complexes bearing nile red chromophore and one of its derivative: Theoretical evaluation of PDT-related properties.

The outcomes of DFT-based calculations are here reported to assess the applicability of two synthesized polypyridyl Ru(II) complexes, bearing ethynyl nile red (NR) on a bpy ligand, and two analogues, bearing modified-NR, in photodynamic therapy. The absorption spectra, together with the non-radiative rate constants for the S1 - Tn intersystem crossing transitions, have been computed for this purpose. Calculations evidence that the structural modification on the chromophore destabilizes the HOMO of the complexes thus reducing the H-L gap and, consequently, red shifting the maximum absorption wavelength within the therapeutic window, up to 620 nm. Moreover, the favored ISC process from the bright state involves the triplet state closest in energy, which is also characterized by the highest SOC value and by the involvement of the whole bpy ligand bearing the chromophore in delocalising the unpaired electrons. These outcomes show that the photophysical behavior of the complexes is dominated by the chromophore.

Constructing multiple heterogeneous interfaces in one-dimensional carbon fiber materials for superior electromagnetic wave absorption

Due to impedance mismatch and a single loss mechanism, carbon fiber fails to meet the requirements for efficient absorbers in terms of lightweight construction and broad absorption band. In this study, we have successfully prepared one-dimensional beaded SiO2@SiC@C nanofiber (SSCF) composites with multiple heterogeneous interfaces by employing the electrospinning-carbothermal reduction method. The beaded SSCF composites effectively address the impedance mismatch issue by controlling silicon dioxide and silicon carbide through carbothermal reduction. This optimization enriches the defects and interfaces of carbon fibers composites, consequently enhancing the electromagnetic wave absorption performance. The SSCF composites demonstrate remarkable performance, with a minimum reflection loss of −59.53 dB at a matched thickness of 2.21 mm and a maximum absorption bandwidth of 6 GHz. This outstanding performance is attributed to the synergistic effects of the multi-phase composition, bead structure, and one-dimensional network structure. These features not only optimize impedance matching but also enhance defect loss, interface polarization loss (SiC/SiO2, C/SiO2, SiC/C, C/Air), conduction loss, and relaxation loss of the SSCF composites. Furthermore, radar cross-section analysis utilizing computer simulation technology confirms the excellent attenuation of microwave energy by the SSCF composites under realistic far-field conditions. This study provides valuable insights for designing efficient one-dimensional carbon-based electromagnetic wave absorbers.

Characterization and investigation of biofabricated ZnO nanoparticles using Caulerpa sertularioides for antioxidant and antibacterial purposes

Nanoparticles synthesized from marine macroalgae have garnered significant attention in biomedical research due to their potential applications. In this study, zinc oxide nanoparticles (ZnO NPs) were synthesized using an extract from Caulerpa sertularioides (Cs) as a reducing agent. The synthesized C. sertularioides-mediated zinc oxide nanoparticles (Cs-ZnO NPs) were characterized by UV–visible spectroscopy, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Field emission scanning electron microscopy (FE-SEM), High-resolution transmission electron microscopy (HR-TEM), and Dynamic light scattering (DLS) techniques. In the UV–visible spectroscopy analysis, the maximum absorption peak was observed at 364 nm. XRD analysis confirmed that the Cs-ZnO NPs had a crystalline structure. FE-SEM and HR-TEM demonstrated that the Cs-ZnO NPs were mostly spherical in shape and the size ranged between 20 and 87 nm. The zeta size and potential of Cs-ZnO NPs at 97.89 nm and 14.1 mV were confirmed by DLS analysis. The antioxidant activities were tested by various in vitro assays, and the results demonstrated that Cs-ZnO NPs exhibit dose-dependent antioxidant activities. Further, Cs-ZnO NPs were highly effective against Vibrio harveyi both as an antibacterial and anti-biofilm agent. The toxicity assessment of Cs-ZnO NPs on Artemia nauplii indicated moderate toxicity. Overall, this study concludes that Cs-ZnO NPs have potential application in the aquaculture industry to prevent pathogenic illnesses and enhance disease resistance without causing adverse effects.

Design and optimization of a corrugated tubular shell structure based on triply periodic minimal surface

A novel corrugated tubular shell structure based on triply periodic minimal surface (TPMS) was proposed in this study. The initial diamond tubular thin-walled structure (D-TTS) and corrugated tubular thin-walled structures (C-TTS) model were designed and then fabricated using selective laser melting (SLM). The 3D-printed model deviation distribution was obtained by using computed tomography (CT) scanning. Compressive behaviors and energy absorption capacity of the tubular thin-walled structures were investigated using experimental and numerical methods. To obtain optimal designs of C-TTS, a surrogate model was established and multi-objective optimization was carried out. The maximal specific energy absorption (SEA) and the minimal peak crushing force (PCF) were obtained by non-dominated sorting genetic algorithm II (NSGA-II). Compared with the initial D-TTS, maximal SEA is increased by 9.34%, and the minimal PCF is reduced by 58.96%. This structure enhances the diversity of tubular structure designs while also inspiring innovative approaches for developing energy absorption devices and structures utilizing TPMS.

Synthesis, optical properties, and dual‐color halochromic fluorescence of novel π‐conjugated polymers bearing coumarin unit in the main chain

AbstractA series of novel π‐conjugated polymers bearing alternating coumarin and phenylene units in the main chain backbone was synthesized via Sonogashira coupling reaction. The red‐shifts in the absorption maxima of the polymers indicate the expansion of π‐conjugated system in the polymer main chains. These polymers exhibited strong green fluorescence in organic solvents. Clearly perceptible dual‐color halochromic fluorescence was confirmed for the polymers by the significantly reversible changes of emission color from green to blue during alkalization and acidification processes. The lactone ring opening and closing property in the coumarin molecule functioned as a controllable switch, broadening the applications of the coumarin‐based π‐conjugated polymers as acid–base responsive fluorescence materials.

Highly Twisted Ladder Oligosilanes Bearing Phenyl and tert‐Butyldimethylsilyl Groups

Two stereoisomers of bicyclic ladder oligosilanes bearing phenyl and tert‐butyldimethylsilyl groups were synthesized, and their structures and electronic properties are compared with previously reported perisopropyl‐substituted analog. These novel ladder oligosilanes have highly twisted structures with the twist angles between the two terminal Si–Si bonds of av. 37.7 and 39.8°. The UV spectra of these compounds show bathochromically shifted absorption maxima with the longest wavelength compared with that of the perisopropyl‐substituted bicyclic ladder oligosilane. The electronic properties of the ladder oligosilanes were analyzed by theoretical calculations.

Investigation of structural, electronic, optical and thermoelectric properties of hallide double perovskite Rb2AlAgX6 (X = Cl, I): A first-principles DFT study

In order to meet the demands of the energy consumption, double perovskites (DP) are a dependable green energy source. Consequently, there is a great deal of promise for thermoelectric and optoelectronic device applications when studying these perovskite halides. Our work examined the thermoelectric and optoelectronic properties of Rb2AlAgCl6 and Rb2AlAgI6 halides using Density Functional Theory (DFT). The tolerance factor and energy of formation for the halides that were examined show that they are stable in the cubic phase, structurally and thermodynamically. We calculated the bandgaps for Rb2AlAgCl6 (Eg = 3.82 eV) and Rb2AlAgI6 (Eg = 1.321 eV) using mBJ potentials, and compared them to the reported values. The optical characteristics of the materials under investigation were revealed through the use of a complicated dielectric function. The computed optical findings show that the materials are suitable for optoelectronic applications, with maximal light absorption occurring in the ultraviolet (UV) and infrared (IR) ranges. Optical parameters obtained includes large values of absorption coefficients (∼105cm−1), low reflectivity (∼1–15 %), and high optical conductivity (∼1015 sec−1). Thermoelectric properties revealed enhanced power factor for Rb2AlAgI6 as compared to Rb2AlAgCl6. These results imply that these materials are appropriate for application in optical and thermoelectric devices.

First-principles screening of optoelectronics and thermoelectric response of XAcTe2 (X=K, Rb) full Heusler alloys: mBJ+SOC effect

Structural geometry, Electronic, optical, and thermoelectric attributes of XAcTe2 (X=K,Rb) full Heuser alloys were investigated theoretically via density functional theory (DFT). Structural optimization yielded optimized lattice parameters along with obtained negative formation energies (Ef) revealed the thermodynamically stable cubic geometries of alloys under investigation. For both alloys, the computed electronic band dispersions exhibit semiconductor behavior with a direct band gap. The band gap value of KAcTe2 is 1.59 eV, and 1.66 eV for RbAcTe2. The analysis of optical response shows maximum absorption α (ω) in the ultraviolet (UV) region, validating their quality for photovoltaic devices. The investigation of thermoelectric characteristics showed that both alloys display higher electrical conductivities and lower thermal conductivities.

MXene/cobalt ferrite/carbon materials based composites for efficient microwave absorption

In the present study, cobalt ferrite (CF) nanoparticles were in-situ grown on MXene/carbon-based materials (activated carbon (AC), MWCNT, and GO) to develop composites via facile hydrothermal route. The MXene/CF/MWCNTs composite (FMCNT4) achieved an excellent maximum reflection loss (RLmax) of −67.04 dB at 16.24 GHz & a thickness of 5.94 mm, whereas at the thickness of 5.86 mm, the FMCNT4 obtained a maximum effective absorption bandwidth (EAB, RL < −10 dB) of 2.73 GHz. On the other hand, replacing MWCNTs with AC in the composite (FMAC4) showed RLmax of −46.52 dB at 18 GHz and 5.1 mm thickness, it also got an EAB of 2.54 GHz at 5.5 mm thickness. The MXene/CF/GO composite (FMGO5) obtained RLmax = −17.31 @ 17.12 GHz & 6 mm. The composite having MWCNTs showed the best performance, and the reason for this remarkable MW absorption performance originated from the high impedance matching followed by dielectric polarization and magnetic losses in the composite. The formation of multiple heterointerfaces between MXene, CF, and MWCNTs enhanced the interfacial polarization, whereas the conducting MXene and MWCNTs also contributed to conduction polarization. Thus, the present investigation showcases FMCNT as an excellent synergetic nanocomposite for MW absorption applications.

Doping Engineering To Modulate Surface Plasmon Resonance and Enzyme-like Activities for Enhancing Photoacoustic Imaging-Guided Targeted Cancer Therapy in the Second Near-Infrared Window.

Biological imaging-guided targeted tumor therapy has been a soughtafter goal in the field of cancer diagnosis and treatment. To this end, we proposed a strategy to modulate surface plasmon resonance and endow WO3-x nanoparticles (NPs) with enzyme-like catalytic properties by doping Fe2+ in the structure of the NPs. Doping of the Fe2+ introduced oxygen vacancies into the structure of the NPs, inducing a red shift of the maximum absorption wavelength into the near-infrared II (NIR-II) region and enhancing the photoacoustic (PA) and photothermal properties of the NPs for more effective imaging-guided cancer therapy. Under NIR-II laser irradiation, the Fe-WO3-x NPs produced very strong NIR-II PA and photothermal effects, which significantly enhanced the PA imaging and photothermal treatment effects. On the other hand, Fe2+ in Fe-WO3-x could undergo Fenton reactions with H2O2 in the tumor tissue to generate ·OH for chemodynamic therapy. In addition, Fe-WO3-x can also catalyze the above reactions to produce more reactive oxygen species (ROS) and induce the oxidation of NADH to interfere with intracellular adenosine triphosphate (ATP) synthesis, thereby further improving the efficiency of cancer therapy. Specific imaging of tumor tissue and targeted synergistic therapy was achieved after ligation of a MUC1 aptamer to the surface of the Fe-WO3-x NPs by the complexing of -COOH in MUC1 with tungsten ions on the surface of the NPs. These results demonstrated that Fe-WO3-x NPs could be a promising diagnosis and therapeutic agent for cancer. Such a study opens up new avenues into the rational design of nanodiagnosis and treatment agents for NIR-II PA imaging and cancer therapy.