Broad Absorption Research Articles

Joule heat induced ultrafine ZrO2/C composites for enhanced microwave absorption

Lightweight absorbers with effective broad absorption and high thermal stability are highly desirable in the field of electromagnetic wave absorption. In this work, we introduce a facile carbon thermal shock method to prepare ZrO2/C composites using UIO 66 (Zr) as the precursor. The instant heating and cooling process ensures the uniform deposition of nano-sized ZrO2 (ca. 5–15 nm) on graphene, exhibiting an ultrahigh interfacial number density of ca. 1015 m−2 that favors polarization loss. Due to the synergetic effect of dielectric loss and impedance matching, the prepared ZrO2/graphene composites show tunable wide-microwave absorption performance by adjusting the heat temperature, and possess a wide absorption band covering the entire X and Ku band. Notably, the ZrO2/graphene composites show high thermal stability up to 1000 °C, which presents great potential for microwave absorption applications.

M-Pyripentaphyrins(1.0.0.0.0): BIII Complexes and β-β Directly Linked Dimers.

m-Pyripentaphyrins(1.0.0.0.0) were synthesized by Suzuki-Miyaura coupling of 3,5-bis(5-borylpyrrol-2-yl)-BODIPY with 2,6-dibromopyridine. Upon treatment with PhBCl2, pyripentaphyrin 1 provided mono- and bis-BIII complexes sequentially. The Mono-BIII complex shows a distorted tetrahedral coordinated BIII with a σ-phenyl ligand on the BIII and the bis-BIII complex shows an additional distorted tetrahedral coordinated BIII with a B-H bond. Bromination of the pyripentaphyrins with N-bromosuccinimide (NBS) resulted in regioselective formation of 8-bromopyripentaphyrins, which were dimerized to 8,8'-linked dimers by reductive coupling with Ni(cod)2. While all these pyripentaphyrins are nonaromatic, they exhibit characteristic broad absorption bands at long wavelength near the NIR region, indicating the presence of effective macrocyclic conjugation.

One‐Pot Synthesis of Conductive Metal–Organic Framework@polypyrrole Hybrids with Enhanced Electromagnetic Wave Absorption Performance

Rational heterostructure design can bring interfacial polarization relaxation to significantly enhance the electromagnetic wave (EMW) absorption performance. However, intelligently building a homogeneous heterostructure with superior EMW absorption properties remains a great challenge. Herein, a typical conductive metal–organic framework Cu3(HHTP)2 (hexahydroxytriphenylene, HHTP) is delicately packed onto a polypyrrole (PPy) conductive polymer surface via a one‐step in situ polymerization approach. Results show that Cu3(HHTP)2 is well packed on the PPy surface to form an elegant Cu3(HHTP)2@PPy hybrids interfacial microstructure with a unique superiority regarding EMW absorption compared with single components of PPy and Cu3(HHTP)2. Interestingly, the interfacial microstructure of Cu3(HHTP)2@PPy hybrids can be tuned by adjusting the composition of the PPy and Cu3(HHTP)2, resulting in the improvement of impedance matching, conductive loss, and enhancement of interfacial polarization relaxation, endowing the optimization of the EM wave absorption properties of the Cu3(HHTP)2@PPy. The broad effective absorption bandwidth covers a range as broad as 6.68 GHz (11.00–17.68 GHz), which is higher than most reported metal‐organic frameworks (MOFs) and conductive polymer‐based EM absorbing materials. Herein, new insight for developing highly efficient EMW absorption materials through hybridized interfacial microstructure engineering is provided.

Discovery of a damped Ly α absorber in the circumnuclear zone of the FeLoBAL quasar SDSS J083942.11+380526.3

ABSTRACT SDSS J083942.11+380526.3 ($z=2.315$) is an iron low-ionization broad absorption lines quasar that exhibits visible Balmer absorption lines (H $\alpha$), implying a significant $n=2$ population. The quasar also shows an array of absorption lines, including O i, Ni ii, Fe ii, Mg ii, Al iii to C iv, and N v. The high-ionization absorption lines such as C iv and Si iv are revealed by slightly blueshifted broad absorption lines troughs. The resonance doublets such as Mg ii and Al iii are saturated but did not reached zero intensity which indicates that the broad-line region (BLR) is partially covered. Overall, however, the absorption is predominantly from low-ionization Fe ii lines, emitted from ground and excited states up to at least 3.814 eV. This implies that the absorbing gas spans the hydrogen ionization front and extends into the partially ionized zone where neutral hydrogen is certainly present. Notably, the hydrogen line spectrum of the quasar shows no signature of expected Ly $\alpha$ absorption. Instead, the line spectrum shows an unusual Ly $\alpha$ emission characterized by a fully filled emission line spectrum which is a composite of a strong narrow core superposed on a weak broad base. Taking into account the effect of partial covering to BLR, we have extracted a strong Damped Ly α systems (DLA) trough in Ly $\alpha$ emission region. To fit the spectrum, we performed photoionized model calculations and compared them to the observations. We found that photoionization modelling using cloudy can successfully reproduce the main characteristics of the quasar spectrum, and the predicted neutral hydrogen column density arising from the clouds responsible for the low-ionization absorption provides a good match to the extracted DLA trough. This indicates that both the DLA and the low-ionization absorption arise from the same medium that is roughly collocated with the dusty torus.

Tunable wideband terahertz absorber based on single-layer patterned graphene

In this study, we propose and validate a broadband terahertz perfect absorber. The absorber has a simple structure, which consists of a gold (Au) substrate, a TOPAS dielectric layer and a patterned graphene layer. By the simulations, a broad absorption band can be obtained with a high absorption above 90% between 3.31 THz and 7.15 THz, and the relative bandwidth reaches 73.4%. Meanwhile, the absorption higher than 99% is between 3.81 THz and 6.6 THz with a relative bandwidth of 53.6%. The mechanism of the surface excited plasma (SPP) and electromagnetic dipole resonance are responsible for its almost perfect broadband absorption. By changing the Fermi energy level of the graphene layer, the flexible broadband absorption spectra can be acquired. By varying the geometrical parameters of the structure, a wider spectral range of absorption wavelengths can be realized. For both TE and TM polarization, the absorption can remain above 90% over a wide range of incidence angles. Due to the independent tunability and high absorption of the proposed device, it has great potential applications in terahertz imaging, smart absorption, detectors and communications.

Enhancing Power Conversion Efficiency of Organic Solar Cells with Magnetoplasmonic Fe3O4@Au@m-ABS Nanoparticles.

Organic-inorganic nanocomposites have the potential to be used in photovoltaic materials due to their eco-friendliness, suitable band gaps, and high stability. In this work, we integrated gold and Fe3O4 magnetic nanoparticles with poly-m-amino benzene sulfonic (m-ABS) to synthesize Fe3O4@Au@poly-(m-aminobenzenesulfonic acid) (Fe3O4@Au@m-ABS) magneto-plasmonic nanoparticles (MPNPs) to enhance the performance of the organic photovoltaic (OPV). These MPNPs exhibit broad UV-Vis absorption and a low band gap of 2.878 eV, enhancing their suitability for photovoltaic applications. The MPNPs were introduced into the ZnO electron transporting layer (ETL) and active layer to investigate the influence of MPNPs on the power conversion efficiency (PCE) of the OPVs. When 0.1 vol% MPNPs were incorporated in the ETL, the OPVs achieved a PCE of 14.24% and a fill factor (FF) of 69.10%. On the other hand, when 0.1 vol% MPNPs were incorporated in the active layer, the OPVs showed a PCE of 14.11% and an FF of 68.83%. However, the OPVs without MPNPs only possessed a PCE of 13.15% and an FF of 63.69%. The incorporation of MPNPs increased the PCE by 8.3% in the OPV device. These findings suggest that Fe3O4@Au@m-ABS MPNPs are promising nanocomposite materials for enhancing the performance of OPVs.

Broadband microwave absorption and antibiosis effect of Cu@C@Fe3O4 nanocomposites

Metal Cu nanoparticles have been recognized as the long-standing presence in the fields of antibacterial and low-induced bacterial resistance, however, the uncontrollable Cu ion concentration from Cu nanoparticle leads to the unstable release of copper ions, limiting their controllable antibacterial application. Based on stable release of copper ions from Cu@C nanocapsules, herein, we report a novel A/B/C structure Cu@C@Fe3O4 nanocomposite to present integrated functionalities of highly controllable antibiosis and electromagnetic wave (EMW) absorption to realize a bifunctional EMW absorption system. With stable concentration, the Cu@C@Fe3O4 nanocomposite can slowly release Cu ions to experience an efficient reactive oxygen species process to realize extreme stable antibiosis behavior and long-term antibacterial effect that is 100 % bactericidal effect. With the sustained antibacterial conditions, the Cu@C@Fe3O4 with magnetic component simultaneously exhibits a good impedance matching to lead a broad microwave absorption with a bandwidth of 5.87 GHz. Considering above two functions, the multifunctional Cu@C@Fe3O4 provides a pathway for multifunctional EMW absorption materials exploration in antibacterial and microwave absorption applications. This strategy also indicates the possibility to functionalize magnetic nanocapsules towards even broader applications.

Construction of direct Z-scheme Co9S8/CdS with tubular heterostructure through the simultaneous immobilization and in-situ reduction strategy for enhanced photocatalytic Cr(VI) reduction under visible light

Tubular Co9S8/CdS heterostructures have been successfully synthesized by in-situ growing CdS onto Co9S8 nanotubes through a simultaneous immobilization and in-situ reduction strategy. It turned out that the so-obtained heterostructure with Co9S8/CdS molar ratio of 1/10 can display a broad light absorption edge and especially much enhanced capacity for photocatalytic reduction of Cr(VI) under visible light. The characterization analysis and experimental results suggested that an interfacial electrostatic field between Co9S8 and CdS elements in the heterostructure could be constructed due to their different Fermi levels, allowing for more quantities of highly reductive electrons to participate in the photocatalytic reaction. Therefore, the so-obtained Co9S8/CdS (1/10) heterostructures could achieve the photocatalytic reduction efficiency of 100% within 20 min, which was more than two and four times larger than that of pristine CdS and Co9S8, respectively. Moreover, the possible photocatalytic reaction mechanism for reducing Cr(VI) was investigated and found to follow the direct Z-scheme charge transfer pathway. This novel fabrication route for composite photocatalysts with tubular heterostructures could lead to the widespread implementations for the elimination of various harmful pollutants in the process of environmental governance.

Advanced acoustic design: 3D printed thermoplastic folded core sandwich structures with porous materials and microperforations for enhanced sound absorption

This study introduces a novel sound-absorbing sandwich structure with a folded core, created through 3D printing technology, to address the challenge of weak sound absorption in the low-frequency range in sound absorption materials (SAMs). The structure comprises chopped carbon fiber–dispersed thermoplastic polyamide (CF-PA), continuous carbon fiber (CCF) filaments, and polyurethane (PU) foam coated with graphene oxide (GO). Simulation studies revealed that optimized structural parameters and microperforation diameters resulted in enhanced sound absorption coefficient (SAC) of 99 % or more at 1250 Hz, within the low-frequency range (160–1600 Hz). The GO-coated PU foam SAMs demonstrated excellent sound absorption performance measured in the high-frequency range (1600–6000 Hz), achieving 99 % SAC at 2400 Hz. Furthermore, the manufactured folded core structure exhibited outstanding sound absorption performance, achieving SAC of 99 % at 732 Hz measured in the low-frequency (160–1600 Hz) band and 99 % at 600 Hz, showcasing broad absorption capabilities measured in the high-frequency band (160–6000 Hz). Additionally, a flatwise compression test on the structure filled with GO-coated PU foam demonstrated a 32 % improvement in compressive load, indicating the structure’s versatility for various applications.

Enhancing photocatalytic dye degradation efficiency through the utilization of shock wave effects on neodymium oxide (Nd2O3)

This article delves into the impact of shockwaves on neodymium oxide (Nd2O3) nanoparticles, aiming to evaluate their physical and chemical stability. Nd2O3 nanoparticles were subjected to varying sets of shock pulses (100, 200, and 300) in photocatalytic dye degradation. The nanoparticles crystallinity and unit cell volume after shockwave exposure were examined using powder X-ray diffraction (PXRD) analysis with unit-cell software. PXRD data revealed no alterations in the crystalline structure, lattice parameter and unit cell volume. Comparisons between pre- and post-shockwave field emission scanning electron microscopy (FE-SEM) portraying data demonstrate that repeated shockwave application causes a decrease in particle size. Raman spectroscopy, under ambient conditions, shows a high intensity after shock conditions intensity will decrease. Furthermore, FTIR spectroscopy revealed the characteristic strong and broad absorption band associated with metal-oxygen (Nd-O) groups in the Nd2O3 nanoparticles. UV–Vis diffuse reflectance spectroscopy (DRS) was used to investigate the bandgap of the Nd2O3 nanoparticles. Initially, the bandgap was measured at 5.96 eV under ambient conditions, but following the shockwave exposure, it was decreased to approximately 5.91 eV. Interestingly, the surface area of the shockwave-treated Nd2O3 nanoparticles is increased and exhibited an increased efficiency in photocatalytic dye degradation. This finding holds promising implications for environmental remediation applications.

Broad absorption line quasars in the Dark Energy Spectroscopic Instrument Early Data Release

ABSTRACT Broad absorption line (BAL) quasars are characterized by gas clouds that absorb flux at the wavelength of common quasar spectral features, although blueshifted by velocities that can exceed $0.1c$. BAL features are interesting as signatures of significant feedback, yet they can also compromise cosmological studies with quasars by distorting the shape of the most prominent quasar emission lines, impacting redshift accuracy and measurements of the matter density distribution traced by the Lyman $\alpha$ forest. We present a catalogue of BAL quasars discovered in the Dark Energy Spectroscopic Instrument (DESI) survey Early Data Release, which were observed as part of DESI Survey Validation, as well as the first two months of the main survey. We describe our method to automatically identify BAL quasars in DESI data, the quantities we measure for each BAL, and investigate the completeness and purity of this method with mock DESI observations. We mask the wavelengths of the BAL features and re-evaluate each BAL quasar redshift, finding new redshifts which are $243\, {\rm km}\, {\rm s}^{-1}$ smaller on average for the BAL quasar sample. These new, more accurate redshifts are important to obtain the best measurements of quasar clustering, especially at small scales. Finally, we present some spectra of rarer classes of BALs that illustrate the potential of DESI data to identify such populations for further study.

Ultralight Hierarchical Fe3O4/MoS2/rGO/Ti3C2Tx MXene Composite Aerogels for High-Efficiency Electromagnetic Wave Absorption.

Aerogel-based composites, renowned for their three-dimensional (3D) network architecture, are gaining increasing attention as lightweight electromagnetic (EM) wave absorbers. However, attaining high reflection loss, broad effective absorption bandwidth (EAB), and ultrathin thickness concurrently presents a formidable challenge, owing to the stringent demands for precise structural regulation and incorporation of magnetic/dielectric multicomponents with synergistic loss mechanisms within the 3D networks. In this study, we successfully synthesized a 3D hierarchical porous Fe3O4/MoS2/rGO/Ti3C2Tx MXene (FMGM) composite aerogel via directional freezing and subsequent heat treatment processes. Owing to their ingenious structure and multicomponent design, the FMGM aerogels, featured with abundant heterogeneous interface structure and magnetic/dielectric synergism, show exceptional impedance matching characteristics and diverse EM wave absorption mechanisms. After optimization, the prepared ultralight (6.4 mg cm-3) FMGM-2 aerogel exhibits outstanding EM wave absorption performance, achieving a minimal reflection loss of -66.92 dB at a thickness of 3.61 mm and an EAB of 6.08 GHz corresponding to the thickness of 2.3 mm, outperforming most of the previously reported aerogel-based absorbing materials. This research presents an effective strategy for fabricating lightweight, ultrathin, highly efficient, and broad band EM wave absorption materials.

Efficiency enhancement of novel ITO/ZnSe/CNTs thin film solar cell

This study presents a novel photovoltaic cell design utilizing a layered structure of Indium Tin Oxide (ITO), Zinc Selenide (ZnSe), and Carbon Nanotubes (CNTs) for enhanced solar energy conversion. We employed the Solar Cell Capacity Simulator (SCAPS-1D) to model and optimize the device under AM 1.5 spectrum conditions. Our simulations systematically investigated the influence of key parameters including layer thicknesses, doping concentrations, temperature, back contact work function, and parasitic resistances on cell performance. The optimized structure demonstrated a theoretical power conversion efficiency of 29.91%, with an open-circuit voltage (Voc) of 799 mV, a short-circuit current density (Jsc) of 43.49 mA/cm², and a fill factor (FF) of 86.02%. These promising results are attributed to the synergistic combination of CNTs' broad spectral absorption, ZnSe's effective charge separation, and optimized layer properties. We found that the CNT absorber layer's doping concentration significantly impacted cell performance, with an optimal value of 10¹⁷ cm⁻³. The ZnSe buffer layer thickness showed minimal effect on efficiency within the studied range. Temperature increases from 300 K to 400 K led to a significant efficiency drop from 33.97% to 24.65%, primarily due to Voc reduction. While these results represent idealized conditions and upper theoretical limits, they provide valuable insights for the potential of CNT-based solar cells. This study offers a roadmap for future experimental work in high-efficiency thin-film photovoltaics, highlighting the promise of novel material combinations and the importance of device architecture optimization.

Biopreparation of titanium dioxide nanoparticles mediated by Calendula officinalis flower extract for catalytic reduction of 4-nitrophenol and treatment of allergic conjunctivitis

This study investigates the an eco-friendly synthesis for the production of titanium dioxide nanoparticles (TiO2 NPs) by employing the water-soluble flower extract of Calendula officinalis as a natural reducing and stabilizing agent. The green produced TiO2 NPs/C. officinalis were characterized using different advanced analytical techniques, including FT-IR, FE-SEM, EDS-elemental mapping, XRD, ICP-OES and TEM. It represents the TiO2 NPs were found to be spherical in shape and well distributed without agglomeration. It also revealed the particle sizes were in the range of 30–50 nm. EDX represented the Ti atomic species along with C and O are seen to be well-dispersed in a homogeneous manner. The broad absorption band appeared at 3200–3450 cm−1 assigned to OH bond stretching belong to the adsorbed water over the titanium dioxide nanoparticles. Further, newly synthesized TiO2 NPs/C. officinalis are used as a nanocatalyst for the reduction of 4-nitrophenol (4-NP). A UV–Vis spectrophotometer is employed to track the effectiveness of the reduction process. Recyclability in 8 further degradation cycles is used to assess the sustainability of this catalyst, and the results show a steady and notable degradation activity. After a week of daily treatment, the allergic conjunctivitis clinical scores in Dunkin-Hartley guinea pigs were evaluated. The guinea pigs were sensitized with intraperitoneal ovalbumin and then subjected to topical conjunctival challenge. Different doses of TiO2 NPs/C. officinalis (20 and 100 µg/kg), prednisolone (30 mg/kg), chlorpheniramine (10 mg/kg), or PBS (10 mL/kg) were administered. The levels of serum Immunoglobulins were measured by ELISA. It was observed that the levels of ovalbumin-specific IgE notably decreased. Notably, the treatment with TiO2 NPs/C. officinalis at both doses led to a notably lower clinical score for allergic conjunctivitis. Furthermore, the TiO2 NPs/C. officinalis-treated guinea pigs conjunctival tissue showed mild mononuclear infiltration compared with the intense conjunctival tissue inflammatory infiltration observed in the PBS-treated group. These data suggest that TiO2 NPs/C. officinalis may have clinical efficacy in alleviating allergic conjunctivitis.

Photoluminescence emission enhancement in the LiSrVO4:Eu3+ vanadate phosphor by partial substitution of M+ ions (M+=Li+/Na+/K+); optical thermometry; and optical transition probabilities using Judd-Ofelt analysis

In solid state lighting (SSL), pcWLEDs gain more attention for various illumination applications. The Eu3+ activated LiSrVO4:xEu3+ (0–15 mol% in steps of 3) phosphors are prepared by the conventional solid state method and their phase formation is confirmed by PXRD. It suggest that the samples are in a monoclinic structure with P2/m space group. SEM results confirmed that the size of the prepared phosphor is in a micrometer range with an irregular spherical shape. The optical diffuse reflectance spectrum (DRS) consisted broad band absorption in the ultraviolet (UV) region (270–350 nm) and also, they are found to absorb strongly the NUV light (396 nm) and the blue light (466 nm). They exhibit the strongest emission at 617 nm for the samples under 326 nm excitation. The PL intensity of the phosphors are improved by co-doping. The optical transition probabilities of the LiSrVO4:9 mol% Eu3+ phosphor are also analyzed using the Judd-Ofelt theory. The optimized phosphor showed a good thermal stability and the lifetime values are in the millisecond range. The absolute and the relative sensitivities are obtained from the temperature dependent lifetime measurements. The LiSrVO4:9 mol%Eu3+ phosphor yielded CIE coordinates (x, y) of (0.5987, 0.4005), a low CCT of 1468K, and a color purity of 96.4 %. These results indicate the potential application of the LiSrVO4 based phosphors in WLEDs.

Non-uniform polarization boosted electromagnetic wave absorption with high efficiency and a broad frequency range

3-Aminobenzene sulfonic acid (mASA) has been co-polymerized into polyaniline (PANI) surface layers of ferrite nano particles by oxidative polymerization method. The sulfonic group of mASA anchored into PANI molecular have been employed as a dopant of PANI to partially substitute the dissociative dopant, hydrochloric acid (HCl). Owing to the constrained local distribution of mASA in PANI, the non-uniform polarization of PANI has been successfully stimulated by sulfonic acid doping. This results in various scattering loss modes and refined impedance matching in the synthesized ferrite/PANI nano-composite, which contributes to excellent absorbing properties with a high reflection loss of −56.42 dB and a broad effective absorption bandwidth of 3.8 GHz. The exhibited performances in microwave absorption are superior to most of ferrite-related composites. The explored strategy provides a novel way to tailor microwave absorbing composites to enhance their comprehensive microwave absorbing properties.

Broad Light Absorption and Multichannel Charge Transfer Mediated by Topological Surface State in CdS/ZnS/Bi2Se3 Nanotubes for Improved Photocatalytic Hydrogen Production

AbstractSemiconductor heterojunctions have garnered extensive interest in photocatalytic hydrogen generation, yet the limited light absorption and charge transfer efficiencies still restrict the photocatalytic performance. The topological insulator has unique surface states and high‐mobility electrons, demonstrating the significant potential for enhancing photocatalysis. Herein, a ternary photocatalyst based on a topological insulator, in which CdS and ZnS nanoparticles are grown on Bi2Se3 nanotube, is prepared for efficient photocatalysis driven by topological surface state for the first time. Under simulated solar light irradiation, the CdS/ZnS/Bi2Se3 nanotubes display a robust photocatalytic hydrogen production rate of 7.13 mmol h−1 g−1, which is 69.2 times of CdS and comparable to many CdS‐based photocatalysts. The unique hollow structure, topological surface state of Bi2Se3, and cooperative bandgap excitations of the three components endow the hybrids with wide light response to harvest solar energy. Meanwhile, the multichannel charge transfer facilitated by topological surface state and internal electric fields within the hybrids effectively suppresses the recombination of the photogenerated charge carriers. This mechanism maintains a high concentration of stable electrons on Bi2Se3, resulting in highly efficient hydrogen production. This work provides a new inspiration for designing heterojunction photocatalysts based on topological insulators for high‐efficiency solar‐driven energy conversion.

Recent Development and Advancement in Quantum Dots in Pharmaceutical and Biomedical Fields for the Delivery of Drugs

Abstract: Nanoscale semiconductors known as quantum dots (QDs) are essential for drug testing because they bridge the gap between nanotechnology and the testing of drugs. QDs are a valuable tool in theranostics and treatment because of their unique physicochemical features. Due to their photoluminescence and electronic properties, including broad and continuous absorption spectra, narrow emission spectra from visible to near-infrared wavelengths, and long-lasting and high brightness, they are suitable probe materials for use in (bio)sensing (immunological) platforms. Several studies use QDs due to their optical, magnetic, electrical, photochemical, and biological features that allow them to be employed in various scientific domains. When utilized in drug delivery systems, fluorescent markers, such as QDs, can track the metabolism of drugs in the human body. Many medicinal applications, such as disease diagnosis and medication research, can benefit from these fluorescent tests. In this review article, the application of QD in drug delivery and immunoassay sensing has been described in detail.

Spectral properties and photophysical processes of triphenylamine-porphyrin-pyrimidine triads

Porphyrins have attracted considerable attention as an important family of photosensitizers used for dye-sensitized solar cells (DSSCs). In this work, a novel triphenylamine-porphyrin-pyrimidine triad with a triple bond linkage was synthesized and characterized. The sensitizer presents broad absorption in solution and on TiO2 films across the UV-Vis region benefiting from the extended conjugation. The acetenyl [Formula: see text]-conjugated bridge stimulates the photoinduced electron transfer (PET) process and brings a charge-separated state lifetime of around 4 μs. DSSC devices based on the sensitizer achieve a power conversion efficiency (PCE) of 3.77% thanks to the prolonged charge-separated state lifetime and suppressed charge recombination. The understanding of the structural, optical, and electrochemical properties of triphenylamine-porphyrin-pyrimidine triads provides new insights into the rational design of porphyrin sensitizers for various applications.

Broadband sensitized near-infrared emission in Eu2+-Nd3+ co-doped BaAl2O4 as a potential spectral modulator for silicon solar cells.

The near-infrared (NIR) down-conversion process for broadband sensitization has been studied in Eu2+-Nd3+ co-doped BaAl2O4. This material has a broad absorption band of 200-480 nm and can convert photons in the visible region into NIR photons. The NIR emission at 1064 nm, attributed to the Nd3+:4F3/2 → 4I11/2 transition, matches the bandgap of Si, allowing Si solar cells to utilize the solar spectrum better. The energy transfer (ET) process between Eu2+ and Nd3+ was demonstrated using photoluminescence spectra and luminescence decay curves, and Eu2+ may transfer energy to Nd3+ through the cooperative energy transfer (CET) to achieve the down-conversion process. The energy transfer efficiency (ETE) and theoretical quantum efficiency (QE) were 68.61% and 156.34%, respectively, when 4mol% Nd3+ was introduced. The results indicate that BaAl2O4:Eu2+-Nd3+ can serve as a potential modulator of the solar spectrum and is expected to be applied to Si solar cells.