Full-spectrum Light Research Articles

In Situ Construction of Interface with Photothermal and Mutual Catalytic Effect for Efficient Solar-Driven Reversible Hydrogen Storage of MgH2.

Hydrogen storage in MgH2 is an ideal solution for realizing the safe storage of hydrogen. High operating temperature, however, is required for hydrogen storage of MgH2 induced by high thermodynamic stability and kinetic barrier. Herein, flower-like microspheres uniformly constructed by N-doped TiO2 nanosheets coated with TiN nanoparticles are fabricated to integrate the light absorber and thermo-chemical catalysts at a nanometer scale for driving hydrogen storage of MgH2 using solar energy. N-doped TiO2 is in situ transformed into TiNxOy and Ti/TiH2 uniformly distributed inside of TiN matrix during cycling, in which TiN and Ti/TiHx pairs serve as light absorbers that exhibit strong localized surface plasmon resonance effect with full-spectrum light absorbance capability. On the other hand, it is theoretically and experimentally demonstrated that the intimate interface between TiH2 and MgH2 can not only thermodynamically and kinetically promote H2 desorption from MgH2 but also simultaneously weaken Ti─H bonds and hence in turn improve H2 desorption from the combination of weakened Ti─H and Ti─H bonds. The uniform integration of photothermal and catalytic effect leads to the direct action of localized heat generated from TiN on initiating the catalytic effect in realizing hydrogen storage of MgH2 with a capacity of 6.1wt.% under 27 sun.

Full-spectrum radiative cooling for enhanced thermal and electrical performance of bifacial solar photovoltaic modules: A nationwide quantitative analysis

Bifacial photovoltaic (bPV) technologies have been garnering increasing attention in recent years due to their ability to generate more power than conventional PV systems. Passive radiative cooling through spectrally selective absorption/emission is considered one of the most practical and cost-effective solutions for the thermal management of bPV modules. In this study, a full-spectrum radiative cooling (FRC) strategy was proposed to maximize the thermal and electrical performance of bPV modules by enhancing above-bandgap absorption, sub-bandgap reflection, and thermal radiation. A multi-physics model was established to characterize bPV performance, enabling analysis of the module's spectral and thermal responses to full-spectrum light under dynamic weather conditions. The proposed model was validated through outdoor experiments with a commercial bPV module, demonstrating good prediction accuracy. To quantify the radiative cooling effect of the ideal FRC strategy and compare it with the ideal traditional radiative cooling (TRC) strategy, a nationwide simulation analysis was conducted across 32 cities in China. The results indicate that the ideal FRC strategy can achieve an annual average temperature reduction of 2.3–4.4 °C and an additional power gain of 7.3%–8.4% for commercial bPV modules. In comparison, the ideal TRC strategy can only achieve an annual average temperature reduction of 1.1–2.2 °C and an additional power gain of 0.38%–0.89%. Results from correlation analysis and sensitivity analysis show that among environmental parameters, wind speed has the most significant positive effect on lowering module temperature, while precipitable water vapor has a relatively small negative impact. Overall, this research demonstrates that the FRC strategy holds great potential for reducing temperature and boosting power output in PV devices, paving the way for promoting the development of sustainable and efficient PV systems.

Comparative Transcriptome Analysis Reveals the Light Spectra Affect the Growth and Molting of Scylla paramamosain by Changing the Chitin Metabolism.

Light is an essential ecological factor that has been demonstrated to affect aquatic animals' behavior, growth performance, and energy metabolism. Our previous study found that the full-spectrum light and cyan light could promote growth performance and molting frequency of Scylla paramamosain while it was suppressed by violet light. Hence, the purpose of this study is to investigate the underlying molecular mechanism that influences light spectral composition on the growth performance and molting of S. paramamosain. RNA-seq analysis and qPCR were employed to assess the differentially expressed genes (DEGs) of eyestalks from S. paramamosain reared under full-spectrum light (FL), violet light (VL), and cyan light (CL) conditions after 8weeks trial. The results showed that there are 5024 DEGs in FL vs. VL, 3398 DEGs in FL vs. CL, and 3559 DEGs in VL vs. CL observed. GO analysis showed that the DEGs enriched in the molecular function category involved in chitin binding, structural molecular activity, and structural constituent of cuticle. In addition, the DEGs in FL vs. VL were mainly enriched in the ribosome, amino sugar and nucleotide sugar metabolism, lysosome, apoptosis, and antigen processing and presentation pathways by KEGG pathway analysis. Similarly, ribosome, lysosome, and antigen processing and presentation pathways were major terms that enriched in FL vs. CL group. However, only the ribosome pathway was significantly enriched in up-regulated DEGs in VL vs. CL group. Furthermore, five genes were randomly selected from DEGs for qPCR analysis to validate the RNA-seq data, and the result showed that there was high consistency between the RNA-seq and qPCR. Taken together, violet light exposure may affect the growth performance of S. paramamosain by reducing the ability of immunity and protein biosynthesis, and chitin metabolism.

Efficient Z scheme-type II charge transfer on the interfaces of PAN/ZnO/CdIn2S4 for the enhanced photocatalytic hydrogen generation

The CdIn2S4/xZnO (CIS/xZnO) and CdIn2S4/12.3ZnO-PANx (CIS/12.3ZnO-PANx, PAN is polyacrylonitrile) photocatalysts were prepared and their activities in photocatalytic water splitting for hydrogen production were studied. Their physicochemical properties were determined by XRD, SEM, TEM, XPS, UV–vis and PEC. The photocatalytic hydrogen evolution under the irradiation with full spectrum light was carried out to evaluate its photocatalytic activity and stability. The catalyst CIS/12.3ZnO-PAN30 exhibits the H2 production rate of 4.31 mmol g−1 h−1, ∼61.5 and 5.8 times that of PAN (0.07 mmol g−1 h−1) and CIS/12.3ZnO (0.74 mmol g−1 h−1), respectively. EPR, VB-XPS, Mott-Schottky analysis illustrate that the Z scheme-type II photo carriers transfer path is formed on the interfaces of the PAN/ZnO/CIS in the CIS/12.3ZnO-PAN30 composite, which is more favorable to the spatial separation and migration of photogenerated carriers with the light irradiation, thus significantly increasing the activity of the photocatalytic production. This work supplies a feasible method for preparation of novel ternary organic-inorganic hybrid photocatalysts.

Constructing a Titanium Silicon Molecular Sieve-Based Z-Scheme Heterojunction with Enhanced Photocatalytic Activity.

Titanium silicon molecular sieve (TS-1) is an oxidation catalyst that possesses a long lifetime of charge transfer excited state, high Ti utilization efficiency, large specific surface area, and good adsorption property; therefore, TS-1 acts as a Ti-based photocatalyst candidate. In this work, TS-1 coupled Bi2MoO6 (TS-1/BMO) photocatalysts were fabricated via a facile hydrothermal route. Interestingly, the optimized TS-1/BMO-1.0 catalyst exhibited a decent photodegradation property toward tetracycline hydrochloride (85.49% in 120 min) under the irradiation of full spectrum light, which were 4.38 and 1.76 times compared to TS-1 and BMO, respectively. The enhanced photodegradation property of the TS-1/BMO-1.0 catalyst could be attributed to the reinforced light-harvesting capacity of the photocatalyst, high charge mobility, and suitable band structure for tetracycline hydrochloride degradation. In addition, the mechanism of photocatalytic degradation of tetracycline hydrochloride by the TS-1/BMO-1.0 catalyst was reasonably proposed based on the band structure, trapping, and ESR tests. This research provided feasible ideas for the design and construction of high-efficiency photocatalysts for contaminant degradation.

Less is more: An oxyfluoride garnet broadband cyan-green phosphor towards highly efficient full-spectrum WLEDs

Full-spectrum lighting has become the development direction for human-centric illumination. However, the reabsorption effect caused by cyan, green and yellow multiple-phosphor packaging leads to low luminous efficiency. In this work, a broadband cyan-green phosphor is proposed to replace the cyan and yellow phosphors for highly efficient and thermally robust full-spectrum WLEDs. A new family of oxyfluoride garnet phosphors Lu2QMg2Al3O9F3: Ce3+ (Q = Ca, Sr, Ba) has been developed by incorporating F- into the classic LuAG: Ce3+ green phosphor. The excess charge was compensated by substituting trivalent Lu3+ and Al3+ with divalent alkaline earth element. The low covalency and phonon energy of fluorine-containing system endow these serial phosphors with efficient and thermally stable blue-shifted emission. The representative Lu2SrMg2Al3O9F3: Ce3+ exhibits a broadband cyan-green emission peaked at 513 nm with a 105 nm FWHM. Furthermore, outstanding quantum efficiency (88.4%) and thermal stability (94.3% @ 423 K) were achieved. This oxyfluoride phosphor was packaged with red phosphor without cyan phosphor on a blue chip. The obtained WLEDs show an excellent color rendering index (Ra = 96.8) with luminous efficiency (LE = 106 lm/W). This research might pave a promising avenue for the development of next-generation full-spectrum lighting.

A nonmetallic plasmonic catalyst for photothermal CO2 flow conversion with high activity, selectivity and durability

The meticulous design of active sites and light absorbers holds the key to the development of high-performance photothermal catalysts for CO2 hydrogenation. Here, we report a nonmetallic plasmonic catalyst of Mo2N/MoO2-x nanosheets by integrating a localized surface plasmon resonance effect with two distinct types of active sites for CO2 hydrogenation. Leveraging the synergism of dual active sites, H2 and CO2 molecules can be simultaneously adsorbed and activated on N atom and O vacancy, respectively. Meanwhile, the plasmonic effect of this noble-metal-free catalyst signifies its promising ability to convert photon energy into localized heat. Consequently, Mo2N/MoO2-x nanosheets exhibit remarkable photothermal catalytic performance in reverse water-gas shift reaction. Under continuous full-spectrum light irradiation (3 W·cm−2) for a duration of 168 h, the nanosheets achieve a CO yield rate of 355 mmol·gcat−1·h−1 in a flow reactor with a selectivity exceeding 99%. This work offers valuable insights into the precise design of noble-metal-free active sites and the development of plasmonic catalysts for reducing carbon footprints.

Full-Spectrum White-Light Emission from Triple Self-Trapped Excitons in Hybrid Mixed-Metal Halides.

Low-dimensional metal halides with broadband emissions are expected to serve as downconversion luminescent materials for solid-state lighting (SSL). However, efficiently generating full-spectrum white-light emission with a high color-rendering index (CRI) in single-phase emitters remains a challenge. Here, we report a novel zero-dimensional (0D) hybrid mixed-metal halide (TPA)2CuAgI4 (TPA = tetrapropylammonium), in which individual [CuAgI4]2- dimers are completely isolated and surrounded by the organic cations TPA+. Cu+ and Ag+ share the same crystallographic site in [CuAgI4]2- dimers with the same statistical probability. Upon photoexcitation, single crystals exhibit a full-spectrum white-light emission with a full width at half-maximum (fwhm) of up to 314 nm and a high quantum efficiency of 46.8%. Detailed photophysical studies and theoretical calculations reveal that the ultra-broadband emission of (TPA)2CuAgI4 originates from the radiative recombination of red-, green-, and blue-emitting self-trapped excitons in [CuAgI4]2- dimers. In addition, (TPA)2CuAgI4 nanocrystals were successfully synthesized and exhibited optical properties similar to those of single-crystal counterparts. Finally, a prototype ultraviolet (UV)-pumped white-light-emitting diode (WLED) and a composite thin film employing this new white-light emitter produces a well-distributed full-spectrum white light with a high CRI of 91.4 and a warm correlated color temperature (CCT) of 4135 K, indicating the potential application of this white-light emitter in SSL. These results provide a new perspective for designing superior single-phase white-light emitters.

Effects of light qualities on growth and physiological-biochemical traits of Scutellaria baicalensis.

Canopy spectral composition significantly affects growth and functional traits of understory plants. In this study, we explored the optimal light condition suitable for enhancing Scutellaria baicalensis's yield and quality, aiming to provide scientific reference for the exploitation and utilization of medicinal plant resources in the understory of forests. We measured the responses of growth, morphology, biomass allocation, physiological traits, and secon-dary metabolites of S. baicalensis to different light qualities. S. baicalensis was cultured under five LED-light treatments including full spectrum light (control), ultraviolet-A (UV-A) radiation, blue, green, and red light. Results showed that UV-A significantly reduced plant height, base diameter, leaf thickness, leaf area ratio, and biomass of each organ. Red light significantly reduced base diameter, biomass, effective quantum yield of photosystem Ⅱ (ФPSⅡ), and total flavonoid concentration. Under blue light, root length and total biomass of S. baicalensis significantly increased by 48.0% and 10.8%, respectively, while leaf number and chlorophyll content significantly decreased by 20.0% and 31.6%, respectively. The other physiological and biochemical traits were consistent with their responses in control. Our results suggested that blue light promoted photosynthesis, biomass accumulation, and secondary metabolite synthesis of S. baicalensis, while red light and UV-A radiation negatively affected physiological and biochemical metabolic processes. Therefore, the ratio of blue light could be appropriately increased to improve the yield and quality of S. baicalensis.

Charge compensator adjusts the luminescence intensity of ZnWO4: Sm3+ full spectrum phosphors: A bifunctional phosphors for plant growth lights and FIR thermometers

Full spectrum white LED plant growth light sources are suitable for use in conditions requiring a high color rendering index. In addition to red and blue light, green light was shown to have a positive impact on plant growth in earlier studies. In this work, a series of Sm3+ doped ZnWO4 phosphors was prepared using the high-temperature solid-state reaction method. Li+ serves as a charge compensator to reduce lattice defects caused by non-equivalent isomorphism. XRD measurements and Rietveld refinement were used to investigate the phase composition and structural properties of the samples. The luminescent properties of the samples were tested using a fluorescence spectrophotometer. The Li + introduction can significantly improve the energy transfer from the matrix to Sm3+ and the luminescence intensity of Sm3+. In addition, this phenomenon was explained with non-equivalent isomorphism and the charge density difference diagram. The LED lamp was prepared using ZnWO4: 0.004Sm3+, 0.004Li + phosphor and LED chip. The emitted full spectrum light can match well with the absorption spectrum of plant pigments. The color rendering index of the LED lamp is greater than 91. And the comparative experiment of plant cultivation shows that the prepared LED plant lamp has good effects. The dependence of luminescence properties of ZnWO4: 0.004Sm3+, 0.004Li+ phosphor on temperature was determined. Based on fluorescence intensity ratio (FIR) technology, the maximum SaMAX and SrMAX are 52 % K−1 at 453 K and 9.31 % K−1 at 303 K, respectively. As the temperature increases, the chromaticity shift (Δs) value is 0.254. The benefits of the ZnWO4: 0.004Sm3+, 0.004Li+ phosphor are the straightforward synthesis process, low cost, pure phase, full spectrum, high color rendering index, tunable red-to-blue ratio, and temperature monitoring function. Therefore, this phosphor is an ideal material in plant growth and optical temperature measurement.

Breaking Through the Luminescence Stability Bottleneck of Oxyfluoride Phosphor for Sun‐Like Led Lighting

AbstractSunlight like optical source is the primary objective of healthy lighting. In contrast, achieving full spectrum lighting with high stability remains challenging, mostly due to the scarcity of purple chip‐pumped cyan‐green phosphors and their inherent emission instability. In this study, a novel strategy is presented that realizes simultaneous enhancements in both humidity stability (increased by 2.9 times) and luminescence quantum efficiency (enhanced by 1.5 times) for cyan‐emitting Sr3AlO4F:Ce3+ phosphor by employing Si/N doping. Theoretical modelling shows that these improvements are attributed to the regulation of energy bands and structural rigidity as well as modulation of the ionicity of chemical bonds. Furthermore, blending the other violet chip‐pumped phosphors, sun‐like LEDs that accurately replicate solar spectra in different times of the day with an optimal color rendering index of 99 is successfully engineered. Moreover, the universality of this strategy on other oxyfluoride phosphors has also been validated. This groundbreaking outcome offers a practical solution to overcome the inherent luminescence stability limitations in oxyfluoride phosphors, thus catalyzing the application of these cyan‐green candidates in sun‐like LED lighting.

0D/2D Bi2WO6:Yb3+,Tm3+/Bi12O17Cl2 S-scheme heterojunction photocatalyst with enhanced full spectrum light activity by upconversion luminescence

To effectively utilize near-infrared light in the solar spectrum, expanding the spectral response range of photocatalysts is one of the main issues at present. Herein, a novel 0D/2D Bi2WO6:Yb3+, Tm3+/Bi12O17Cl2 S-scheme heterostructure with full spectral response is successfully synthesized through a hydrothermal method. The optimized Bi2WO6:Yb3+,Tm3+/Bi12O17Cl2 (1:1) photocatalyst degraded 68.2% and 59.1% of methylene blue (MB) and Rhodamine B (RhB) at 980 nm NIR light irradiation for 240 min, and the degradation of MB and RhB was 96.1% and 92.3% under visible light irradiation for 40 min, respectively. The enhanced photocatalytic activity could be attributed to these synergistic effects including the unique 0D/2D contact interface, the expanded photoresponse range, enhanced upconversion luminescence, as well as efficient energy transfer process between Yb3+/Tm3+ and Bi2WO6. Based on characterization and photocatalytic experiments, the introduction of Bi2WO6:Yb3+, Tm3+ can construct S-scheme heterojunctions with Bi12O17Cl2 and produce a full-spectrum response to sunlight. The result, the Bi2WO6:Yb3+, Tm3+/Bi12O17Cl2 photocatalysts possessed effective charge distribution and migration and maintained the excellent redox capacity of semiconductor materials. The hydroxyl radicals (·OH), superoxide radicals (·O2), and holes (h+) as active species played crucial roles in the degradation process. This work describes a potential method to construct S-scheme photocatalyst with great upconversion activity that possesses full spectral response for water pollution control.

Improvement in productivity of strawberry (Fragaria X ananassa Duch.) under vertical farming system

Vertical farming has evolved keeping in view the constraints of space due to the increasing population and shrinking agricultural land. Although vertical farming is more associated with small-duration crops, especially vegetables, flowers, and annuals such as strawberry can also be grown through the selection of appropriate variety and farming structure. An experiment was conducted to evaluate the effect of full spectrum light on the growth, flowering, fruiting, and yield of strawberry under a vertical farming system. Results revealed that plant height, plant spread, petiole length, number of leaves, number of fruits, average berry weight, and average yield were highest at light intensity of 175–200 μmol s-1m-2. It was observed that in T1 when plants were at the fourth level or top level (L4) of verticals under natural light, were superior in comparison to plants at lower levels in T2 (L3), T3 (L2), and T4 (L1) due to decreasing light intensity down to the base of verticals. The plants grown with an additional supply of artificial full spectrum light (AFSL) at these lower levels had performed better in T5 (2 h at L3), T6 (4 h at L2) and T7 (6 h at L1) in terms of growth, flowering, fruiting, and yield of strawberry and were at par to T1. In the vertical farming system, space, water, nutrient, and light optimization is possible as it ensures efficient resource utilization such as precision agriculture. Thus, the supply of AFSL is important to ensure sustainable yield in vertical farming.

Tuning Eu2+ luminescence in Sr8CaLu (PO4)7via Na+-induced local structure engineering for violet-chip-excitable full-spectrum lighting

We develop a new type of violet-light-excitable Eu2+:Sr8CaLu(PO4)7 phosphor with tunable green–yellow emissions and high photoluminescence quantum yields above 70% via Na+ alloying-induced local structural modification.

Ag4Br6] cluster-based 3D bromoargentate hybrid: crystal structure, optical/photoelectrical performance and theoretical study.

The self-assembly of cluster-based halide framework materials has been a matter of great interest but with great challenges. Herein, by exploiting hexamethylenetetramine (Hmta) with Td symmetry as a structural modifier, we successfully constructed and systematically characterized an unusual three-dimensional (3D) hybrid bromoargentate, namely K[NH4][Ag4Br6(Hmta)] (1), bearing a diamond-type [Ag4Br6(Hmta)]n2n- anionic skeleton built up from adamantane-like units of inorganic [Ag4Br6] clusters and organic Hmta ligands. UV-Vis diffuse reflectance analysis showed that the optical bandgap of the title compound was 2.68 eV, indicating a visible-light-responsive semiconductive behavior. More importantly, upon alternate light illumination, the so-designed compound exhibited remarkable photoelectric switching properties, with photocurrent densities (0.38 and 1.10 μA cm-2 for visible and full-spectrum light, respectively) that compete well with and even exceed those of some high-performance metal halide counterparts. Further theoretical calculations, including band structure, density of states, and wave functions, revealed that compound 1 has a unique valence band and conduction band distribution, rendering it with small effective masses (especially the electrons), which may be responsible for its good photoelectricity. Furthermore, in this work, Hirshfeld surface analysis, thermogravimetric analysis, and X-ray photoelectron spectroscopy (XPS) studies were performed.

Structure modification and luminescence regulation in new violet light excitable Sr(2-y)BayY4La4(SiO4)6O2:xEu2+ phosphors via cation substitution.

Cyan-emitting phosphors are urgently needed to address the "cyan gap" in artificial full-spectrum lighting. In this research, a series of Sr(2-y)BayY4La4(SiO4)6O2:xEu2+ (0.005 ≤ x ≤ 0.08, 0.0 ≤ y ≤ 2.0) phosphors with tunable luminescence was synthesized. Through cation regulation, the luminescence color of Sr(2-y)BayY4La4(SiO4)6O2:xEu2+ can be adjusted from yellow to cyan. Crystal structure analysis revealed that Eu2+ ions simultaneously occupy [Sr1/Ba1Y1La1] and [Sr2/Ba2Y2La2] sites, resulting in multiple luminescence centers and a broadened emission spectrum. With increasing Ba2+ ion concentration, the PLE spectrum was red-shifted from 337 nm to 372 nm, and the excitation intensity in the violet region was significantly enhanced, making it more compatible with violet LED chips. Meanwhile, the PL spectrum was blue-shifted from 543 nm to 496 nm with increasing Ba2+ concentration, accompanied by an increase of about 10 times in the excitation and emission intensity. The optimized Ba2Y4La4(SiO4)6O2:0.02Eu2+ phosphor can be excited by violet light and emits bright cyan light effectively, which can be used to fill the "cyan gap". Eventually, a series of white LED devices was manufactured by combining the as-prepared luminescence-tunable phosphors with commercial phosphors. Among them, the 410 nm violet LED chip-based WLED(Ba2) device comprising Ba2Y4La4(SiO4)6O2:0.02Eu2+ exhibited the best electroluminescence performance, increasing the color rendering index from 82.0 to 98.6, verifying the compensation effect of the Ba2Y4La4(SiO4)6O2:Eu2+ phosphor on cyan light.

In situ fabrication of a plasmonic Bi@Bi2O2CO3 core-shell heterostructure for photocatalytic CO2 reduction: structural insights into selectivity modulation.

The precise design of active sites and light absorbers is essential for developing highly efficient photocatalysts for CO2 reduction. Core-shell heterostructures constructed based on large-sized plasmonic Bi metals are ideal candidates because of the utilization of full-spectrum light and effective charge separation. However, the mechanism of selectivity modulation of large-sized Bi@semiconductor photocatalysts has yet to be explored in depth. Herein, a plasmonic Bi@Bi2O2CO3 core-shell heterostructure was successfully synthesized via a facile solvothermal treatment in deep eutectic solvents, demonstrating highly efficient photocatalytic CO2 reduction. This structure features a sizeable Bi sphere with a thin, epitaxially grown Bi2O2CO3 shell, which allows for the utilization of the entire light spectrum. Additionally, the oxygen vacancies in the Bi2O2CO3 shell can rapidly trap electrons transferred from the Bi core via Bi-O-Bi bonds, thereby forming abundant electron-rich interfaces that serve as the active sites for activating reactant molecules and facilitating the reaction.

An efficient blue-violet phosphor: an advanced material designed for high-quality full-spectrum lighting.

A highly efficient phosphor with exceptional luminescence properties is crucial for achieving high-quality solid-state white-light illumination. Here, this paper presents a groundbreaking discovery, an innovative blue-violet emitting Ba1.31Sr3.69(BO3)3Cl:Ce3+ (BSBCl:Ce3+) phosphor designed with remarkable thermal stability and quantum efficiency for full spectrum white light-emitting diodes (WLEDs). By employing a high-temperature solid-phase method, we synthesized various BSBCl:xCe3+ phosphors with different Ce3+ doping concentrations. Remarkably, BSBCl:0.03Ce3+ displays a broad excitation band from 250 nm to 400 nm, rendering it compatible with commercial near-ultraviolet (UV) LED chips. Under 330 nm excitation, this phosphor emits blue light with an astonishing 88.2% internal quantum efficiency (IQE) and an impressive 60.9% external quantum efficiency (EQE). Notably, when employed in the temperature range of 298-473 K, the synthesized BSBCl:0.03Ce3+ phosphor exhibits exceptional color stability and thermal stability (I423 K/I298 K = 83%). Utilizing BSBCl:0.03Ce3+ as the blue-violet emitting component in the fabrication of WLED devices has demonstrated significant advancements in the color rendering index. These findings underscore the potential of BSBCl:Ce3+ phosphors for a wide range of applications in health-oriented indoor illumination.

Double-plasmonic-coupled heterojunction photocatalysts for highly-efficient full-spectrum-light-driven H2 evolution from ammonia borane

Methods to enhance the full-spectrum-light-driven water splitting for H2 evolution remain one of the critically important issues to explore advanced photocatalysts. In this study, we present a novel double-plasmon-coupled semiconductor heterojunction photocatalyst with a large number of oxygen vacancies, produced via a simple two-step solvothermal process. These materials represent a new model system to study the kinetics process and catalytic activity of ammonia borane hydrolytic dehydrogenation in a full-spectrum-light-driven plasmonic semiconductor heterostructure. Upon irradiation with full-spectrum light, the resultant photocatalysts are capable of delivering H2 generation rate up to 13,031 μmol g-1h−1, which is ∼6 times greater than that of pristine MoO3-x counterpart. The excellent photocatalytic behavior is primarily attributed to the improved carrier separation, increased light absorption, and enhanced generation of “hot electrons”, enabled by a synergistic photo- and thermo-catalytic effect. Consequently, the high performance of the novel photocatalyst derives from the design of a double-plasmonic-coupling effect and the photocatalyst containing Type-Ⅱ heterojunctions.

Enhanced photocatalytic properties of MWCNTs-decorated SrTiO3–SrCO3 hierarchical structures achieved by efficient charge transfer

Cr (VI) is a heavy metal ion that cannot be ignored in industrial wastewater and is highly toxic, posing a serious threat to the health and safety of natural organisms. In order to remove Cr (VI) ions in the wastewater, photocatalysis is currently employed and becomes a promising and effective way but the photocatalytic rate still needs further improvement. In this work, multi-walled carbon nanotubes (MWCNTs) modified SrTiO3–SrCO3 microspheres with a three-dimensional porous structure were prepared by a facile solvothermal method. When the dosage of MWCNTs was 0.55 wt%, the obtained sample exhibited the highest photocatalytic efficiency, with approximately 100 % removal of Cr (VI) within 6 min and the photocatalytic rate constant (k) can reach 0.52 min−1 under full-spectrum light irradiation. The enhancement in the photocatalytic performance is probably attributed to the large surface area for more adsorption of Cr (VI) ions on the sample and effectively transfer of photo-generated carriers via the hetero-structures for the reaction of Cr (VI) ions with more carriers. Therefore, this work can provide a facile method for the preparation of photocatalysts with good performance for the removal of Cr (VI) in the wastewater.