Search Results (19)

A novel catalyst, Tm₂FeSbO₇, was synthesized by employing the solid-phase high-temperature sintering method, and, for the first time, it was utilized to create a Z-type heterojunction with BiYO₃. A direct Z-scheme Tm₂FeSbO₇/BiYO₃ heterojunction photocatalyst (TBHP) was successfully produced by employing the ball-milling technique. X-ray diffraction analysis results indicated that Tm₂FeSbO₇ crystallized in a cubic pyrochlorestructure which owned the Fd-3m space group, with a unit cell parameter of 10.1769 Å, whereas BiYO₃ displayed a fluorite structure in the Fm-3m space group, with a unit cell parameter of 5.4222 Å. The Mossbauer spectrum of Tm₂FeSbO₇ showed that Fe³⁺ ions might locate at octahedral sites. The measured bandgap widths for the TBHP, Tm₂FeSbO_7, and BiYO₃ were 2.14 eV, 2.21 eV, and 2.30 eV, respectively. Multiple experimental results demonstrated that the TBHP exhibited a higher valence band ionization potential, a narrower band gap width, and a higher removal efficiency of the sulfamethoxazole (SMX) compared with the Dy₂TmSbO₇/BiHoO₃ heterojunction photocatalyst. Under visible-light irradiation (VISLI) of 115 min, the TBHP showcased exceptional photocatalytic elimination performance; therefore, the elimination rate of the SMX and the total organic carbon (TOC) mineralization rate reached 99.51% and 98.10%, respectively. In contrast to single-component Tm₂FeSbO₇, BiYO_3, or conventional nitrogen-doped titanium dioxide (N-TiO₂) catalyst, the TBHP exhibited removal efficiency enhancement for degrading the SMX by 1.17 times, 1.31 times, or 4.06 times. Simultaneously, the matching mineralization rate for removing the TOC density by employing the TBHP was 1.20 times, 1.34 times, or 4.73 times higher than that by employing Tm₂FeSbO₇, BiYO₃, or conventional N-TiO₂. Above experimental results indicated that the mineralization efficiency for removing TOC density by employing the TBHP was higher than that by employing Tm₂FeSbO₇, BiYO₃, or N-TiO₂. Radicals trapping experiments and the electron paramagnetic resonance spectroscopy results revealed that hydroxyl radicals, superoxide anions, and photoinduced holes were the primary active species during the catalytic elimination course of the SMX by employing the TBHP under VISLI. The results demonstrated that the direct Z-scheme TBHP, which was developed in this study, exhibited the maximal removal efficiency for degrading the SMX in contrast to Tm₂FeSbO₇, BiYO₃, or N-TiO₂. Additionally, the possible elimination routes and elimination mechanisms of the SMX were proposed. Therefore, an important scientific foundation for developing high-performance heterojunction catalysts was established. Full article

The escalating prevalence of counterfeiting and forgery has imposed unprecedented demands on advanced anti-counterfeiting technologies. Traditional luminescent materials, relying on single-mode or static emission, are inherently vulnerable to replication using commercially available phosphors or simple spectral blending. Multimode luminescent materials exhibiting excitation wavelength-dependent emission offer significantly higher encoding capacity and forgery resistance. Herein, we report the colloidal synthesis of lanthanide-doped Cs₂ZrCl₆ nanocrystals (Ln³⁺ = Tb, Eu, Pr, Sm, Dy, Ho) via a robust hot-injection route. These nanocrystals universally exhibit efficient host-to-guest energy transfer from self-trapped excitons (STEs) under 254 nm, yielding sharp characteristic Ln³⁺ f–f emission alongside the intrinsic broadband STE luminescence. Critically, Tb³⁺ enables direct 4f → 5d excitation at ~275 nm, while Eu³⁺ introduces a low-energy Eu³⁺ ← Cl⁻ LMCT band at ~305 nm, completely bypassing STE emission. Due to their multimode luminescent characteristics, we fabricate a triple-mode anti-counterfeiting label displaying different colors under different types of excitation. These findings establish a breakthrough excitation-encoded multimode platform, offering potential applications for next-generation photonic security labels, scintillation detectors, and solid-state lighting applications. Full article

We establish a general, device-oriented procedure to extract absolute pump-band metrics from room-temperature UV–Vis (ultraviolet–visible) absorbance—including the absorption coefficient α(λ), per-active-ion cross-section ${\sigma }_{\mathrm{e}\mathrm{f}\mathrm{f}}\left(\lambda \right)$, the effective per-active-ion absorption cross section ${\sigma }_{\mathrm{e}\mathrm{f}\mathrm{f}}\left(\lambda \right)$ and derivative-based line-shape descriptors. As a representative case study, the procedure is applied to nanocrystalline Er³⁺/Ho³⁺:Y₃Ga₅O₁₂ over the 350–700 nm spectral range. After baseline correction and line-shape inspection assisted by the numerical second derivative of the absorbance, we extract conservative peak positions and the full width at half maximum across the visible 4f–4f manifolds. At the technologically relevant pump wavelengths near 406 nm (Er-addressing) and 473 nm (Ho-addressing) bands, resulting absorption coefficients are α = 0.313 ± 0.047 cm⁻¹ and α = 0.472 ± 0.071 cm⁻¹, respectively. The corresponding per-active-ion ${\sigma }_{\mathrm{e}\mathrm{f}\mathrm{f}}$ of (3.62 ± 0.54) × 10⁻²² cm² and (5.46 ± 0.82) × 10⁻²² cm², referenced to the measured optical path length L = 0.22 ± 0.03 mm (approximately 15% propagated relative uncertainty; explicit 1/L rescaling). Cross sections are reported per total active-ion density (Er³⁺ + Ho³⁺). The spectra exhibit Stark-type substructure only partially resolved at room temperature; the second derivative highlights hidden components, and we report quantitative descriptors (component count, mean spacing, curvature-weighted prominence, and pump detuning) that link line-shape structure to absolute pump response. These device-grade metrics enable rate-equation modelling (pump thresholds, detuning tolerance), optical design choices (path length, single/multi-pass or cavity coupling), and host-to-host benchmarking at 295 K. The procedure is general and applies to any rare-earth-doped material given an absorbance spectrum and path length. Full article

Co_0.95R_0.05Fe₂O₄ nanoparticles were synthesized using a sol-gel approach incorporating bio-based agents and were found to be single phases adopting a cubic Fd-3m structure. XPS shows the presence of Gd³⁺ and Ho³⁺ ions. The spin–orbit splitting of about 15.4 eV observed in Co 2p core-level spectra is an indication that Co is predominantly present as Co³⁺ state, while the satellite structures located at about 6 eV higher energies than the main lines confirm the existence of divalent Co in Co_0.95R_0.05Fe₂O₄. The positions of the Co 3s and Fe 3s main peaks obtained by curve fitting and the exchange splitting obtained values for Co 3s and Fe 3s levels point to the high Co³⁺/Co²⁺ and Fe³⁺/Fe²⁺ ratios in both samples. The saturation magnetizations are smaller for the doped samples compared to the pristine ones. For theoretical magnetization calculation, we have considered that the heavy rare earths are in octahedral sites and their magnetic moments are aligned antiparallelly with 3d transition magnetic moments. ZFC-FC curves shows that some nanoparticles remain superparamagnetic, while the rest are ferrimagnetic, ordered at room temperature, and showing interparticle interactions. The M_S/Ms ratio at room temperature is below 0.5, indicating the predominance of magnetostatic interactions. Full article

Co-doping at Ba and Ti sites with double rare-earth elements has proven an effective strategy for enhancing the dielectric properties of BaTiO₃ ceramics. Among intermediate-sized rare-earth ions, Tb and Ho exhibit amphoteric behavior, occupying both Ba and Ti sites. Investigating the site occupation, defect chemistry, and dielectric effects of Tb and Ho in BaTiO₃ is therefore valuable. In this work, Tb/Ho-co-doped BaTiO₃ ceramics with the composition (Ba_1−xTb_x)(Ti_1−xHo_x)O₃ (x = 0.01~0.10) were fabricated at 1400 °C via solid-state reaction, and their solid solubility and crystal structures are confirmed. Microstructure, dielectric properties, photoluminescence, and valence states of samples with a single phase were systematically studied. Both the lattice parameter a and unit cell volume increase with doping level. The ceramic with x = 0.02 meets the X5S dielectric specification. Ho and Tb ions both demonstrate amphoteric site occupancy: Ho exists solely as Ho³⁺ at both Ba and Ti sites, while Tb exhibits mixed valence states as Ba-site Tb³⁺ and Ti-site Tb⁴⁺. As the doping content increases, the concentration of Tb⁴⁺ at Ti sites decreases, and the quantity of Ba-site Ho³⁺ ions initially increases to a maximum before decreasing. Defect compensation mechanisms within the samples are also discussed. Full article

This review delves into the forefront of upconversion luminescence (UCL) research, focusing on KY₃F₁₀-based compounds, particularly their cubic α-phase. These materials are renowned for their exceptional luminescent properties and structural stability, making them prime candidates for advanced photonic applications. The synthesis methods and structural characteristics of the existing works in the literature are meticulously analyzed alongside the transformative effects of various doping strategies on UCL efficiency. Incorporating rare earth (RE) sensitizer ions such as Yb³⁺, along with activator ions like Er³⁺, Ho³⁺, Nd³⁺, or Tm³⁺, researchers have achieved remarkable enhancements in emission intensity and spectral control. Recent and past breakthroughs in understanding the local structure and phase transitions of single-, double-, and triple-RE³⁺-doped KY₃F₁₀ nanocrystals are highlighted, revealing their pivotal role in fine-tuning luminescent properties. Furthermore, the review underscores the untapped potential of lesser-known crystal structures, such as the metastable δ-phase of KY₃F₁₀, which offers promising avenues for future exploration. By presenting a comprehensive analysis and proposing innovative research directions, this review aims to inspire continued advancements in the field of upconversion materials, unlocking new potentials in photonic technologies. Full article

Q-switched fiber lasers have become reliable light sources for generating high-energy pulses, which can be passively modulated by saturable absorbers with excellent nonlinear optical properties. The composite combining Ag and MXene exhibits a broadband nonlinear response and high modulation depth, making it a promising candidate for saturable absorbers in pulsed lasers. Herein, we demonstrate a Q-switched Tm:Ho co-doped fiber laser centered at 2 µm, where the Ag/MXene composite serves as a saturable absorber to generate pulses. The typical spectrum, pulse train, and radio frequency spectrum of Q-switched pulses were observed, in which the 60 dB signal-to-noise ratio was higher than that of 2 µm Q-switched fiber lasers based on other materials, demonstrating the stability of the output pulses. Additionally, the long-term stability of the laser was evaluated over 2 h, where the well-maintained central wavelength and output power also indicated the robustness of the Q-switched laser. Furthermore, the influence of the pump power on the parameters of Q-switched pulses was also investigated, which is conducive to control the output characteristics of lasers. Specifically, the pulse width of the Q-switched pulse decreased, while the repetition rate, output power, and single pulse energy all increased with the increase in pump power. These experimental results demonstrate the ability of Ag/MXene as a saturable absorber and show its potential for generating high-performance pulses in ultrafast lasers. Full article

Glucose-derived carbon hybrids were synthesized by hydrothermal treatment in the presence of oxidized carbon nanotubes. Additionally, iron and nitrogen functionalities were incorporated into the carbon structure using different methodologies. The introduction of iron and nitrogen in a single step under a H₂ atmosphere favored the formation of quaternary nitrogen and oxidized nitrogen, whereas the incorporation of nitrogen under an N₂ atmosphere after doping the hybrids with iron mainly produced pyridinic nitrogen. The samples were characterized by scanning electron microscopy, X-ray spectroscopy, adsorption isotherms, inductively coupled plasma optical emission spectrometry, and Raman spectroscopy. The presence of iron and nitrogen in the carbons increases the onset potential toward oxygen reduction in KOH 0.1 mol L⁻¹ by 130 mV (0.83 V), in comparison to carbonized glucose, whereas the reaction mechanism shifts closer to a direct pathway and the formation of HO₂⁻ decreases to 25% (3.5 electrons). The reaction rate also increased in comparison to the carbonized glucose, as observed by the decrease in the Tafel slope value from 117 to 61 mV dec⁻¹. Furthermore, the incorporation of iron and nitrogen in a single step enhanced the short-term performance of the prepared electrocatalysts, which may also be due to the higher relative amount of quaternary nitrogen. Full article

A_yB_1−yC_xFe_2−xO₄ (C=Ho,Gd,Al) ferrite powders have been synthesized by the sol-gel combustion route. The X-ray diffraction of the CoHo_xFe_2−xO₄ (x = 0~0.08) results indicated the compositions of single-phase cubic ferrites. The saturation magnetisation of CoHo_xFe_2−xO₄ decreased by the Ho³⁺ ions, and the coercivity increased initially and then decreased with the increase of the calcination temperature. The Mössbauer spectra indicated that CoHo_xFe_2−xO₄ displays a ferrimagnetic behaviour with two normal split Zeeman sextets. The magnetic hyperfine field tends to decrease by Ho³⁺ substitution owing to the decrease of the A–B super-exchange by the paramagnetic rare earth Ho³⁺ ions. The value of the quadrupole shift was very small in the CoHo_xFe_2−xO₄ specimens, indicating that the symmetry of the electric field around the nucleus is good in the cobalt ferrites. The absorption area of the Mössbauer spectra changed with increasing Ho³⁺ substitution, indicating that the substitution influences the fraction of iron ions at tetrahedral A and octahedral B sites. The X-ray diffraction of Mg_0.5Zn_0.5C_xFe_2−xO₄(C=Gd,Al) results confirmed the compositions of single-phase cubic ferrites. The variation of the average crystalline size and lattice constant are related to the doping of gadolinium ions and aluminum ions. With increasing gadolinium ions and aluminum ions, the coercivity increased and the saturation magnetization underwent a significant change. The saturation magnetization of AlMg_0.5Zn_0.5FeO₄ ferrite reached a minimum value (M_S= 1.94 mu/g). The sample exhibited ferrimagnetic and paramagnetic character with the replacement with Gd³⁺ ions, that sample exhibited paramagnetic character with the replacement with Al³⁺ ions, and the isomer shift values indicated that iron is in the form of Fe³⁺ ions. Full article

We propose a simple dumbbell-shaped scheme of a Holmium-doped fiber laser incorporating a minimum number of optical elements. Mode-locking regimes were realized with the help of polymer-free single-walled carbon nanotubes (SWCNTs) synthesized using an aerosol (floating catalyst) CVD method. We show that such a laser scheme is structurally simple and more efficient than a conventional one using a ring cavity and a similar set of optical elements. In addition, we investigated the effect of SWCNT film transmittance, defined by the number of 40 nm SWCNT layers on the laser’s performance: operating regimes, stability, and self-starting. We found that three SWCNT layers with an initial transmittance of about 40% allow stable self-starting soliton mode-locking at a wavelength of 2076 nm with a single pulse energy of 0.6 nJ and a signal-to-noise ratio of more than 60 dB to be achieved. Full article

Integrated wastewater treatment processes are needed due to the inefficient removal of emerging pharmaceuticals by single methods. Herein, an adsorbent-photocatalyst integrated material was fabricated by coupling calcium alginate with sulfur-doped TiO₂/tungsten disulfide (S-TiO₂/WS₂/alginate beads) for the removal of oxytetracycline (OTC) from aqueous solution by an integrated adsorption-photocatalysis process. The semiconductor S-TiO₂/WS₂ hybrid photocatalyst was synthesized with a hydrothermal method, while the integrated adsorbent-photocatalyst S-TiO₂/WS₂/alginate beads were synthesized by blending S-TiO₂/WS₂ with sodium alginate using calcium chloride as a precipitating agent. The physicochemical characteristics of S-TiO₂/WS₂/alginate beads were analyzed using X-ray diffraction , scanning electron microscopy, elemental mapping, X-ray photoelectron spectroscopy, and photoluminescence spectroscopy. The integrated adsorption-photocatalysis process showed enhanced removal from 92.5 to 72%, with a rise in the OTC concentration from 10 to 75 mg/L respectively. The results demonstrated that the adsorption of OTC onto S-TiO₂/WS₂/alginate beads followed the Elovich kinetic model and Redlich–Peterson isotherm models. The formations of H-bonds, cation bridge bonding, and n-π electron donor-acceptor forces were involved in the adsorption of OCT onto S-TiO₂/WS₂/alginate beads. In the integrated adsorption-photocatalysis, surface-adsorbed OTC molecules were readily decomposed by the photogenerated active radical species (h⁺, O₂^•−, and HO^•). The persulfate addition to the OTC solution further increased the photocatalysis efficacy due to the formation of additional oxidizing species (SO₄^•⁻, SO₄⁻). Moreover, S-TiO₂/WS₂/alginate beads showed favorable efficiency and sustainability in OTC removal, approaching 78.6% after five cycles. This integrated adsorption-photocatalysis process offered significant insight into improving efficiency and reusability in water treatment. Full article

In this paper, we have demonstrated a dispersion-managed, high-power, Tm-Ho co-doped ultrashort pulse fiber laser using a single walled carbon nanotube (SWNT) dispersed in polyimide film. An in-line type spectral filter was developed to control the output pulse spectra. Two SWNT films with different modulation depths were examined as a mode-locker. Normal dispersion fiber was used in the fiber laser oscillator, and dependence on net cavity dispersion was investigated. Passive mode-locking was achieved in a wide dispersion range, from −0.319 to +0.101 ps². Stable soliton mode-locking operation and dissipative soliton mode-locking operations were observed. The pumping efficiency was ~3 times higher than that in a Tm-doped fiber laser with a similar configuration. The developed fiber laser showed self-start and stable operations, and this laser is useful for practical applications. Full article

A heterogeneous Fenton-like catalyst with single redox site has a rate-limiting step in oxidant activation, which limited its application in wastewater purification. To overcome this, a bimetallic doping strategy was designed to prepare a heterogeneous Fenton-like catalyst (Fe-Mo/rGO) with a double-reaction center. Combined with electrochemical impedance spectroscopy and density functional theory calculation, it was confirmed that the formation of an electron-rich Mo center and an electron-deficient Fe center through the constructed Fe-O-Mo and Mo-S-C bonding bridges induced a higher electron transfer capability in the Fe-Mo/rGO catalyst. The designed Fe-Mo/rGO catalyst exhibited excellent sulfamethazine (SMT) degradation efficiency in a broad pH range (4.8–8.4). The catalytic performance was hardly affected by inorganic anions (Cl⁻, SO₄²⁻ and HCO₃⁻) in the complicated and variable water environment. Compared to Fe/rGO and Mo/rGO catalysts, the SMT degradation efficiency increased by about 14.6 and 1.6 times in heterogeneous Fenton-like reaction over Fe-Mo/rGO catalyst. The electron spin resonance and radical scavenger experiments proved that ·O₂⁻/HO₂· and ¹O₂ dominate the SMT removal in the Fe-Mo/rGO/H₂O₂ system. Fe and Mo, as active centers co-supported on rGO, significantly enhanced the electron transfer between catalyst, oxidant, and pollutants, which accelerated the reactive oxygen species generation and effectively improved the SMT degradation. Our findings offer a novel perspective to enhance the performance of heterogeneous Fenton-like catalysts by accelerating the electron transfer rate in the degradation of organic pollutants. Full article

To overcome the drawbacks of the single N-doped carbon materials, the further development of dual-heteroatoms (N and S) co-doped electrocatalysts is highly anticipated. Herein, N, S-doping and Fe-based carbon materials were synthesized by pyrolyzing a metal–organic framework (MIL-88) with the addition of N-/N, and S-containing ligands (chitosan and L-Cysteine) in the case of iron salt. The resulting electrocatalyst heat-treated at 850 °C (FeNSC-850) displays superior oxygen reduction reaction (ORR) performances to MIL-88-850, with an overall electron transfer number of 3.97 and a minor yield of HO₂^-% (<2.6%). In addition to the comparable activity to commercial Pt/C in catalyzing the ORR in alkaline solution, the FeNSC-850 also shows higher stability, with a slight decline in half-wave potential (∆E_1/2 = 15 mV) after 5000-cycle scanning of cyclic voltammetry. In view of the multiple Fe-based active sites, the additional S doping within FeNSC-850 creates more FeS_x active sites for boosting the ORR performances in alkaline solution. Full article

We present the results of ex vivo exposure by an ultrafast all-fiber Holmium laser system to porcine longissimus muscle tissues. A simple Ho-doped laser system generated ultrashort pulsed radiation with less than 1 ps pulse width and a repetition rate of 20 MHz at a central wavelength of 2.06 μm. Single-spot ex vivo experiments were performed at an average power of 0.3 W and different exposure times of 5, 30 and 60 s, varying the total applied energy in the range of 1.5–18 J. Evaluation of laser radiation exposure was performed according to the depth and diameter of coagulation zones, ablation craters and thermal damage zones during the morphological study. Exposure by ultrashort pulsed radiation with an average power of 0.3 W showed destructive changes in the muscle tissue after 5 s and nucleation of an ablative crater. The maximum ablation efficiency was about 28% at the ablation depth and diameter of 180 μm and 500 μm, respectively. The continuous-wave radiation impact at the same parameters resulted only in heating of the near-muscular tissue, without ablation and coagulation traces. Exposure to tissue with an average power at 0.3 W of ultrashort pulsed radiation led, within 30 and 60 s, to similar results as caused by 0.5 W of continuous-wave radiation, although with less carbonization formation. Full article