Rare Earth Metals Research Articles

Enhancing Efficiency of Dye-Sensitized Solar Cell using Mn or Ce Doped and Co-doped ZnO Photoanodes with Lawsonia Inermis Natural Dye

Abstract In the present research paper, Mn (transition metal) and Ce (rare earth metal) doped and co-doped ZnO nanoparticles were synthesized using a cost-effective sol-gel technique. As synthesized samples were characterized using X-ray diffraction and field emission scanning electron microscope to examine the structure and morphology respectively. The optical properties were examined by UV-Visible and photoluminescence spectroscopic techniques. The synthesized samples were used as photoanode for the fabrication of dye-sensitized solar cell (DSSC). The utilization of a photoanode, containing Mn and Ce doped and co-doped in ZnO, in DSSC leads to a significant enhancement in photovoltaic conversion efficiency with natural dye lawsonia inermis. Different combinations of Mn or Ce doped and co-doped ZnO nanoparticles were used for testing their effectiveness as photoanode in DSSC. It was observed that the efficiency for Mn and Ce co-doped ZnO photoanode-based DSSC was found to be 0.2118%, which is approximately a 750% increase as compared to bare ZnO photoanode based DSSC. The enhancement in the efficiency of DSSCs was due to the formation of a blocking layer by Mn ions which helps to stop the flow of electrons backward and the broadening of the spectrum region with the help of Ce ions using up/down conversion process also helps to achieve higher efficiency. This enhancement in the efficiency of DSSC may be attributed to the synergic effect of Mn and Ce.

Enhanced hypersensitive (5D0→7F2) transition characteristics of Eu3+ doped β-Ga2O3 microrods

Exploring and realizing the luminescence characteristics of rare earth metal (RE) ions doped gallium oxide (Ga2O3) is crucial for developing optoelectronic device applications. The current research used the solid-state reaction approach to synthesize Ga2O3 microrods doped with various europium (Eu3+) concentrations (0.1, 0.2, 0.3, 0.5, 0.75, and 1 mol). X-ray diffraction (XRD) and Raman spectral analyses confirm the monoclinic structure of β-Ga2O3. The intensity of the Raman phonon modes decreased and a peak shift was observed for Eu:β-Ga2O3. The electron microscopy (SEM, TEM) images depicted a nearly uniform distribution of microrods for undoped and Eu:β-Ga2O3 samples. The interplanar distance (d = 0.290 nm, 0.561 nm, and 0.433 nm), from HR-TEM images, corresponding to (0 0 4), (1 0 0), and (1 0 2) crystallographic orientations confirm the monoclinic structure of β-Ga2O3. The elemental mapping images showed a nearly homogeneous Ga, O, and Eu distribution. The UV–visible diffuse reflectance spectroscopy (UV-DRS) showed a notable reduction in the bandgap as the Eu3+ concentration increased. The emission spectra of Eu: β-Ga2O3 microrods showed a narrow red emission at 612 nm (5D0 → 7F2), which relates to the 5D0 → 7Fj (j = 0, 1, 2, 3) energy level arising from an intra-4f transition of Eu3+ ions upon 394 and 465 nm excitation. The red emission was found to increase with Eu content up to 0.5 mol.%. A quenching of emission due to the multipole–multipole interactions was obtained beyond 0.5 mol.% of Eu. The absolute quantum yield (η) calculated for Eu: β-Ga2O3 (0.5 mol.%) was 3.82 %. The luminescence decay curve using the bi-exponential fit and the average lifetime (τ) of the Eu: β-Ga2O3 (0.5 mol.%) was found to be ∼0.172 ms. CIE chromaticity and correlated color temperature analyses of Eu:β-Ga2O3 microrods yielded a red emission with a superior color purity (93 %). The obtained results suggest that Eu:β-Ga2O3 (0.5 wt.%) microrods could be one of the potential candidates for red light sources.

Construction of La/Al2O3 nanorod-like catalyst with rich basic sites: Enabling efficient conversion of COS-superior selectivity and theoretical insights

The introduction of surface basic sites to COS hydrolysis catalysts can improve H2O activation and COS adsorption, leading to enhanced catalytic performance. However, maximizing the concentration of basic sites remains a challenge due to the limited exposed surface area of these catalysts. Herein, a La/Al2O3 catalyst with abundant alkaline sites to catalyze the hydrolysis of COS was prepared by a simple ammonia-assisted hydrothermal method. This synthesized La/Al2O3 catalyst exhibits a thin rod-like structure formed by the random accumulation of nanoparticles. Lanthanum, one of the most abundant rare earth metals, is an ideal doping aid to further promote the COS-catalyzed hydrolysis performance of Al2O3. Characterization studies show that the proper lanthanum loading effectively enhances the formation of basic sites, leading to improved lattice oxygen reactivity and –OH adsorption capacity. As a result, the prepared La-loaded Al2O3 nanorod sample with abundant basic sites exhibits nearly 100 % COS conversion and total H2S yield at 160 °C. In addition, the reaction pathways and deactivation mechanisms for selective catalytic hydrolysis of COS on the La-doped Al2O3 catalyst were revealed by using in situ DRIFTS to evaluate COS adsorption and hydrolysis. Density functional theory calculations showed that La loading enhances the electron transfer between the La and Al atoms, improves the formation of basic sites, and enhances the adsorption of –OH. This study provides new insights into the design of efficient alumina-based catalysts for the catalytic hydrolysis of COS.

Molecular dynamics simulations of the shear and tensile mechanical properties of rare-earth metal erbium based on deep-learning potential

To gain atomic insights into the physical and mechanical properties of rare-earth metal erbium (Er), performing molecular dynamics (MD) simulations is highly advantageous but has been constrained for lacking of Er interatomic potential. In this work, the essential Er potential for MD simulations was developed by using the deep-potential (DP) method based on first-principles calculations. By systematically comparing the DP-predicated physical properties (melting and solidifying points, elastic properties, etc.) with the results of density functional theory (DFT), experimental or MEAM, we demonstrated that the developed DP model of Er exhibits satisfactory generalization ability and reasonable DFT accuracy on predicting these properties. From the DP-predicted results, we confirmed that the HCP-Er is mechanically stable. The melting point of HCP-Er is 1847 K, while the solidifying point is 1105 K at the cooling rate of 1×1011 K/s. Moreover, we found that the prismatic unstable stacking fault energy of HCP-Er is lower than the basal one, indicating that the Shockley partial dislocation along prismatic planes is easier to slip. The basal/prismatic and prismatic/basal interfaces were discovered during the tensile deformation of HCP-Er single-crystal along the [0001] direction, signifying the occurrence of the parent-to-‘twin’ lattice reorientation. The yield strength of HCP-Er decreases from 5.41 to 5.21 GPa with rising the temperature from 150 to 500 K. The results would be helpful for better understanding the mechanical behaviors of metal Er and further developing the binary or multinary Er-containing DP models.

Tuning the Photophysical and Photochemical Properties of Rare-Earth Cluster-Based Metal–Organic Frameworks

Tuning the Photophysical and Photochemical Properties of Rare-Earth Cluster-Based Metal–Organic Frameworks

Synthesis and characterization of Lanthanum Oxide nanoparticles using Citrus aurantium and their effects on Citrus limon Germination and Callogenesis

The plant extract-mediated method is eco-friendly, simple, safe, and low-cost, using biomolecules as a reducing agent to separate nanoparticles. Lanthanum (La) is a rare earth metal that positively affects plant growth and agriculture. Citrus limon is a leading citrus fruit with many varieties. Conventional vegetative propagation methods depend on season, availability of plant material and are time-consuming. It is the main reason for limiting the acceptance of new varieties. So, In-vitro propagation of the lemon method is practiced overcoming all these problems. Lanthanum oxide nanoparticles (La2O3-NPs) were synthesized using plant extract of C. aurantium. Ultraviolet (UV)-Visible Spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Fourier Transform Infrared (FTIR) spectroscopy, and Thermal Gravimetric Analysis (TGA) were used to characterize the synthesized La2O3-NPs. Fabricated La2O3-NPs were oval and spherical, with an average size of 51.1 nm. UV-visible absorption spectra of La2O3-NPs were shown at a sharp single peak at 342 nm and FTIR showed stretching frequency at 455 cm−1-516 cm−1. In the TGA outcome, mass loss was 9.1%. In vitro experiments demonstrated that La2O3-NPs significantly enhanced the germination and growth of C. limon seeds, achieving an 83% germination rate at 5 mg/L concentration, with uncoated seeds showing root initiation at 10 days and shoot formation at 15 days. Furthermore, La2O3-NPs effectively stimulated callus induction and maturation, with optimal responses observed in media containing MS and 2 mg/L 2,4-D, resulting in a maximum callus frequency of 100% from leaves and 87.5% from shoots at 5 mg/L concentration. These findings underscore the potential of La2O3-NPs to improve seed germination rates, seedling vigor, and callogenesis efficiency, suggesting their promising integration into agricultural practices for sustainable crop production, especially in suboptimal growing conditions. Future research is recommended to explore the mechanisms and broader applications of La2O3-NPs across various plant species and environments.

Rare-Earth Metal Complexes Bearing Electrophilic Carbon and Strongly Polarized Metallacyclopropane Moiety: Synthesis and Diverse Reactivity toward Small Molecules.

Metallacyclopropanes are highly strained and very reactive organometallics; the rare-earth metal complexes bearing both highly reactive electrophilic carbon and strongly polarized metallacyclopropanes are extremely rare. This type of rare-earth metal complexes (κ2-L)RE(η2-C2B10H10)·(THF)3 [L = 1-(2-N-C5H10NCH2CH2)-3-(2,6-iPr2C6H3N═CH)-C8H4N, RE = Lu(1a), Yb(1b), Er(1c), Y(1d), Dy(1e)] bearing the indol-2-yl electrophilic carbon and carboryne-based strongly polarized metallacyclopropanes have been synthesized. Structures of complexes 1 are further confirmed by single-crystal X-ray diffraction and DFT theoretical calculations. It is found that complexes 1 have remarkable reactivity toward different polar unsaturated small molecules, elemental sulfur, and selenium to provide different products (2-15) through the selective reactions of the RE-Ccage, and RE-C2-ind bonds with the given small molecules, respectively. The reactivities of these complexes are different from those of the reported rare-earth metallacyclopropenes and d-block metal-carborynes.

Mechanical study reinforced magnesium-yttrium alloys by eggshell powder using resistance casting

Magnesium-based alloys are relatively new materials for orthopedic implants. One common component that makes magnesium-based alloys biocompatible and chemically stable is the addition of minor compositions of rare earth metals like yttrium to anchor other chemically active components. From an orthopedic perspective, two goals are of primary concern. One is sufficient mechanical support to stabilize the fracture and reduce inflammation. Another is assistance for the transition of osteogenesis and intramembranous ossification for bone production and remodeling. To attain both goals and further improve the current magnesium-yttrium alloys, adding extra ingredients to improve osseointegration is a common and effective approach. By the nature of bone chemistry, calcium is the top choice as calcium is the key element in maintaining bone integrity and biochemical metabolism. In this study, the mechanical behaviors of a calcium-added magnesium-based alloy (Mg-Y3.5 wt%) are investigated by experiments. This inventive idea for the natural source of calcium is obtained from chicken eggs due to their (1) cost-effective and abundant availability, and (2) naturally synthesized calcium carbonate along with a minor content of organic materials. The fabrication processes involved are the ball-milling of eggshells as an additive at 1, 3, and 5 wt%. into magnesium-yttrium alloys and resistance casting to form composites. Material characterization includes microstructural analysis by X-ray diffraction, morphological/elemental analysis via optical microscopy, field emission scanning electron microscopes, energy-dispersive X-ray spectroscopy, mechanical properties by uniaxial compression and Vickers microhardness tests. Experimental results supplemented by statistical and finite element analysis indicate that the new composite exhibits enhanced ductility; and the 3 wt% eggshell-added alloys show better reinforcement of mechanical properties among all samples with an ultimate compression strength of 161.19 MPa, maximum elongation of 17.53 %, and hardness of 457.48 (N/mm2). Note that the comparable mechanical strength of the composite to that of human bones could reduce the stress shielding on bones and further help the process of bone remodeling.

Solar light driven enhanced in photocatalytic activity of novel Gd incorporated ZnO/SnO2 heterogeneous nanocomposites

The Gd-doped ZnO/SnO2 nanocomposites with various atomic percentages (0, 0.5, 0.8, and 1.2 at%) of gadolinium (coded as GdZS0, GdZS1, GdZS2, and GdZS3) was synthesis via the sol–gel method and explored for photodegradation against dye solutions exposing solar light irradiation. The synthesized nanocomposites were characterized employing the XRD, FTIR, FE-SEM, Raman spectroscopy, BET analysis and UV–Vis spectrophotometer. The FE-SEM results indicated that the formation of nanoparticles to nanoflowers covered with Gd ions was observed with an increased doping concentration of Gd. The optical bandgap was evaluated and found in the range of 3.21–3.27 eV for GdZS nanocomposites. The GdZS nano-photocatalysts were investigated against the degradation of different organic dyes and GdZS3 shows the highest degradation efficiencies of 99.3%, 98.3% and 99.4% towards MO, MB and RhB dyes, respectively at neutral pH in aqueous media. Before and after photodegradation. Biological oxygen demand and chemical oxygen demand tests to make estimations of mineralization. The investigations are very promising for the degradation process in rare earth doped metal oxide nanocomposites. A plausible photodegradation mechanism of synthesized nanocomposites under investigation has also been proposed.

Visible-light-prompted photoelectrochemical sensors fabricated using Er3NbO7/P@g-C3N4/SnS2 nanocomposite for detecting mercury ion in environmental water samples

Photoelectrochemical (PEC) detection technology is key for fighting pollution, leveraging the photoelectric conversion of the photoelectrode material. A specialized photoelectrode was developed to detect Hg2+ ions with exceptional sensitivity, utilizing an anodic PEC sensor composed of Er3NbO7/P@g-C3N4/SnS2 ternary nanocomposite. Rare earth metal niobates (RENs) were chosen due to their underexplored potential, whose performance was enhanced through bandgap engineering and surface modification, facilitated by P@g-C3N4 as an immobilization matrix and SnS2, belonging to the I-IV semiconductors category fostering hybrid heterojunction formation for boasting optical properties and suitable redox potentials. Introducing Hg2+ into the system, a specific amalgamation reaction occurs between reduced Hg and Sn. This reaction obstructs electron transfer to the FTO electrode surface, leading to the recombination of charges. The proposed PEC sensor exhibited remarkable analytical performance for Hg2+ detection, high sensitivity, a detection limit of 0.019 pM, excellent selectivity, and a detectable concentration range of 0.002–0.15 nM. Additionally, it demonstrated good recovery and low relative standard deviation when analyzing Hg2+ in water samples, highlighting the potential application of the heterostructure in detecting heavy metal ions via PEC technology.

Carbochlorination of YOCl for Synthesis of YCl3

AbstractAs the production of high-quality titanium (Ti) metal increases significantly, the generation of low-quality Ti scraps increases and exceeds the demand for current cascade recycling in ferrous metallurgy. Therefore, the development of an upgrading recycling technology, in which scraps are refined and reutilized, is required. The magnesium (Mg) deoxidation assisted by the formation of oxychlorides of rare earth metals is currently considered a promising process for upgrading recycling technology, during which YOCl is formed as a byproduct. In this study, we investigate the synthesis and separation of YCl3 from YOCl via carbochlorination at 973 and 1073 K and confirmed that YCl3 can be regenerated from YOCl at a high conversion rate (82.7 pct at maximum). YCl3 was also formed even in the presence of MgCl2; however, MgCl2 decreased the conversion rate (49.8 pct at minimum). The conversion rate in the temperature region where YCl3 is a liquid (1073 K) was lower than that in the temperature region where YCl3 is a solid (973 K). Therefore, an operation with temperature cycling, in which YCl3 is formed at a temperature where YCl3 is a solid and then the temperature is increased to a temperature where YCl3 is a liquid to drain the molten mixed salt, is efficient.

Exploring the synergistically enhanced activity of novel α-MnSe/ppy composite for superior OER catalyst in alkaline medium

The extremely slow kinetics of the water-splitting process stymies the synthesis of hydrogen (H2) from water. To comprehend the main obstacle to the oxygen evolution reaction (OER), it is also necessary to enhance the development of efficient OER electrocatalysts. In this work, manganese selenide with polypyrrole heterostructure is synthesized, described, and electrochemically assessed as an effectiveelectrocatalystfor OER. The novel synthesized materialis characterizedusing a variety of techniques, including scanning electron microscopy (SEM), powder x-ray diffraction (PXRD), transmission electron microscopy (TEM) etc. The unique α-MnSe/ppy composite catalyst is shown to be exceedingly efficient, starting the OER at an astoundingly low voltage of 168 mV (vs. reversible hydrogen electrode [RHE]) at 10 mA cm−2, with a tafel slope of 67 mV dec-1. Also, operando UV–Vis spectro-electrochemical studies give an insight towards the intermediate species formed during the OER catalysis. Under similar electrochemical conditions, the α-MnSe/ppy electrocatalyst outperforms its α-MnSe and ppy counterparts for OER in an aqueous KOH (1.0 M) solution. These results surpass benchmark electrocatalysts made of Mn and rare earth metals. With this invention, a desired non-noble metal is made available that works excellently as an OER electrocatalyst.

Broad spectral response of Y-NaBi(MoO4)2@NaYF4:Yb, Tm photocatalysts for efficient degradation of ciprofloxacin: Upconversion mechanism and theoretical calculations

In this work, a novel Y-NaBi(MoO4)2@NaYF4:Yb, Tm composite was successfully synthesized for the first time by hydrothermal method. The lamellar Y-NaBi(MoO4)2 was dispersed on the surface of the hexagonal prism NaYF4:Yb, Tm without aggregation. The composite achieved a broad spectral response. The NaYF4:Yb, Tm absorbed near-infrared light and emitted ultraviolet and visible light by the energy transfer upconversion process. The emitted light was reabsorbed by Y-NaBi(MoO4)2 through the fluorescence resonance energy transfer process. Moreover, the doping of Y3+ ions enhanced the light response capability of the composite. The experimental results revealed that the photocatalytic degradation efficiency of ciprofloxacin (CIP) reached 96.2 % after 180 min of illumination under simulated sunlight. Meanwhile, the degradation pathways and attack sites of CIP were intensively investigated by liquid chromatography-mass spectrometry analysis and density functional theory theoretical calculations. The upconversion process, the separation of photogenerated carriers and rare earth metal ion doping all contributed to the high effective photodegradation. This work provided a new strategy for effective utilization of solar energy for the degradation of emerging pollutants to mitigate environmental pollution.

Complexation of ThoriumIV with Fluorinated Heterocyclic β‐Diketones in Aqueous Hydrochloric Solutions

AbstractThe interaction of Thorium(IV) with a group of non‐symmetric CF3‐diketones has been studied by means of electronic absorption spectroscopy in HCl aqueous solutions at I=0.5 M (NaCl) and T=298 K. Six heterocyclic dicarbonyl ligands (2‐thenoyl‐trifluoroacetone, 2‐furoyl‐trifluoroacetone, 2‐selenophen‐trifluoroacetone, 2‐tellurophen‐trifluoroacetone, phenyl‐trifluoroacetone, and 2‐naphthyl‐trifluoroacetone) demonstrate the chelation activity toward ThIV in the acidic pH range. Obtained values of the “true” stability constants lie in the range 6.2–6.8 logarithmic units, respectively. A significant (10–15 nm) bathochromic shift between the maximum absorption wavelength of lanthanide and actinide monocomplexes has been detected. Observed spectral shift increases with the atomic number of substituted chalcogen atoms in the heterocyclic ring of the corresponding ligand: 10 nm for furan, 11 nm for thiophen, 14 nm for selenophen, and 15 nm for tellurophene rings. The complexation with Thorium occurs in an acidic media, where studied ligands do not interact with transition and rare earth metals. Spectral and pH shifts make studied ligands useful reagents for the detection and analytical determination of Thorium in the mixture with other metals without prior separation. Quantum‐chemical simulations (DFT and TD‐DFT) demonstrate that the nine‐ and deco‐coordinated structures of ThoriumIV complexes reproduce experimental values within reasonable errors.

Inducing high-concentration Tb3+ with free oxygen via atomic layer deposition

Precise preparation and control of trivalent states in rare earth metal oxide films are crucial for their optical and magnetic applications. In this study, compact and continuous terbium-doped nanofilms were deposited on silica substrates using atomic layer deposition (ALD). The average nanoparticle size varied from 17.9 to 78.5 nm with increasing growth cycles. X-ray photoelectron spectroscopy showed that the Tb3+/Tb4+ ratio increased from 0.98 to 1.42. A valence reduction mechanism involving free oxygen was introduced to analyze the reasons for the enhanced Tb3+ concentration in the nanofilms. The enhanced photoluminescence of Tb3+ (5D4→7F5) ions and the increased magnetization in terbium oxide nanofilms both reveal that free oxygen ions are the effective active sites responsible for the transition from the tetravalent to the trivalent state, in excellent agreement with theoretical analysis. Size control and free oxygen induction are promising strategies for enhancing the optical and magnetic properties of multivalent rare earth oxides.

Efficient Adsorption and Elimination of Tm3+ for Enhanced Seed Germination Using Pillar[5]Arene Polymer.

While rare earth elements (REEs) are essential for modern technology, their production methods raise concerns for agriculture. Researchers are now exploring ways to control and recycle REEs pollution, aiming to minimize agricultural impacts and potentially even develop methods to utilize these elements for improved crop yields. Regarding this issue, a new type of pillar[5]arene polymer (Pol-P[5]-BTZP) has been designed and synthesized by click reaction to enhance the efficiency of adsorption and recovery of rare earth metals. This polymer incorporates the unique structure of 2,6-di-1,2,3-triazolyl-pyridine. The results of various analyses revealed that Pol-P[5]-BTZP exhibits excellent thermal stability, a high specific surface area, and well-distributed networks of micropores and mesoporous structures. The adsorption capacity of Pol-P[5]-BTZP for Tm3+, a representative REE, was evaluated using the Langmuir and Freundlich isothermal adsorption models with a maximum adsorption capacity (Qmax) of 127.71 mg/g. Furthermore, the versatility of Pol-P[5]-BTZP in adsorption and recovering various REEs was tested. In addition to its adsorption capabilities, the potential of Pol-P[5]-BTZP for rare earth recovery and reuse was assessed through experiments on the impact of Tm3+ and La3+ on seed germination. These experiments demonstrated the wide-ranging applicability of Pol-P[5]-BTZP in recovering and reusing REEs for green agriculture.

Synthesis of Rare Earth Metal Complexes Stabilized by Amine Bridged Bis(phenolato) Ligands and Their Performance in the Polymerization of rac-β-Butyrolactone.

A series of rare earth alkoxides bearing amine-bridged bis(phenolato) ligands were synthesized through sequential reactions of RE(C5H5)3(THF) (RE = Y, Lu) or Nd[N(SiMe3)2]3 with bis(phenols) LH2 and CF3CH2OH. Complexes REL(OCH2CF3)(THF)n (1-6) bearing different aryl-substituents were obtained in good yields of 59-70%. They were applied in the ring-opening polymerization (ROP) of rac-β-butyrolactone (rac-BBL), which showed good activity (TOF up to 27,300 h-1), resulting in syndiotactically enriched poly(3-hydroxybutyrate) (PHB) (Pr up to 0.86) with narrow polydispersities (PDI ≤ 1.27). The yttrium complex 3 bearing bulky o-1,1-diphenylethyl substituents outperformed other complexes, suggesting that the smaller ionic radii of metal centers and bulky ortho substituents of ancillary ligands play crucial roles in controlling the activity and stereoselectivity in ROP of rac-BBL. Kinetics of the polymerization of rac-BBL initiated by complex 3 was investigated, which revealed first order dependences on the monomer and initiator concentrations, respectively.

Sorption-Desorption of Rare-Earth Metal Cations by Ferromanganese Crusts of the Govorov Guyot, Magellan Seamounts, Pacific Ocean

Sorption-Desorption of Rare-Earth Metal Cations by Ferromanganese Crusts of the Govorov Guyot, Magellan Seamounts, Pacific Ocean

Lanthanides in the water electrolysis

AbstractThe most feasible technique for producing green hydrogen is water electrolysis. In recent years, there has been significant study conducted on the use of transition metal compounds as electrocatalysts for both anodes and cathodes. Peoples have attempted several strategies to improve the electrocatalytic activity of their original structure. One such technique involves introducing rare earth metals or creating heterostructures with compounds based on rare earth metals. The incorporation of rare earth metals significantly enhances the activity by many folds, while their compounds offer structural stability and the ability to manipulate the electronic properties of the original system. These factors have led to a recent boom in investigations on rare earth metal‐based electrocatalysts. There is currently a pressing demand for a review article that can provide a comprehensive overview of the scientific advancements and elucidate the mechanistic aspects of the impact of lanthanide doping. This review begins by explaining the electronic structure of the lanthanides. We next examine the mechanistic aspects, followed by recent advancements in lanthanide doping and heterostructure formation for water electrolysis applications. It is expected that this particular effort will benefit a broad audience and stimulate more research in this area of interest.image

Construction of CdS nanosphere with rare earth metal modification over acid theory with boosted photocatalytic hydrogen reaction

Absorption of light, surface reaction and carriers transfer are three main aspects that affect the whole photocatalytic process and activity. Surface modification strategy is widely adopted to promote the light response while still presented poor carriers transfer. Therefore, rare earth metal was introduced to regulate the surface property of the photocatalyst, which shows enhanced photocatalytic performance of 4567.0 μmol h−1 g−1 under optimal rare earth doping compare to 1553.3 μmol h−1 g−1 of pure CdS. The addition of Gd could expose more reactive centers and reduce the recombination of photo-generated carriers. Meanwhile, the doping of Gd could extend the light absorption and accelerate the hydrogen production kinetics.