Effective Small Organic Molecule as a Defect Passivator for Highly Efficient Quasi-2D Perovskite Light-Emitting Diodes.

The use of a small organic molecular passivator is proven to be a successful strategy for producing higher-performing quasi-2D perovskite light-emitting diodes (PeLEDs). The small organic molecule can passivate defects on the grain surround and surface of perovskite crystal structures, preventing nonradiative recombination and charge trapping. In this study, a new small organic additive called 2, 8-dibromodibenzofuran (diBDF) is reported and examines its effectiveness as a passivating agent in high-performance green quasi-2D PeLEDs. The oxygen atom in diBDF, acting as a Lewis base, forms coordination bonds with uncoordinated Pb2+, so enhancing the performance of the device. In addition, the inclusion of diBDF in the quasi-2D perovskite results in a decrease in the abundance of low-n phases, hence facilitating efficient carrier mobility. Consequently, PeLED devices with high efficiency are successfully produced, exhibiting an external quantum efficiency of 19.9% at the emission wavelength of 517 nm and a peak current efficiency of 65.0 cd A-1.

Synergistic Surface Modification for High-Efficiency Perovskite Nanocrystal Light-Emitting Diodes: Divalent Metal Ion Doping and Halide-Based Ligand Passivation.

Surface defects of metal halide perovskite nanocrystals (PNCs) substantially compromise the optoelectronic performances of the materials and devices via undesired charge recombination. However, those defects, mainly the vacancies, are structurally entangled with each other in the PNC lattice, necessitating a delicately designed strategy for effective passivation. Here, a synergistic metal ion doping and surface ligand exchange strategy is proposed to passivate the surface defects of CsPbBr3 PNCs with various divalent metal (e.g., Cd2+ , Zn2+, and Hg2+ ) acetate salts and didodecyldimethylammonium (DDA+ ) via one-step post-treatment. The addition of metal acetate salts to PNCs is demonstrated to suppress the defect formation energy effectively via the ab initio calculations. The developed PNCs not only have near-unity photoluminescence quantum yield and excellent stability but also show luminance of 1175 cd m-2 , current efficiency of 65.48 cd A-1 , external quantum efficiency of 20.79%, wavelength of 514 nm in optimized PNC light-emitting diodes with Cd2+ passivator and DDA ligand. The "organic-inorganic" hybrid engineering approach is completely general and can be straightforwardly applied to any combination of quaternary ammonium ligands and source of metal, which will be useful in PNC-based optoelectronic devices such as solar cells, photodetectors, and transistors.

Effective Visible-Light-Driven Photocatalytic Degradation of Harmful Antibiotics Using Reduced Graphene Oxide-Zinc Sulfide-Copper Sulfide Nanocomposites as a Catalyst.

In recent decades, antibiotics have been found in aquatic environments, raising severe concerns. In this study, a unique reduced graphene oxide-zinc sulfide-copper sulfide (rGO-ZnS-CuS) nanocomposite (NC) prepared by using a straightforward surfactant-free in situ microwave method was used for antibiotic degradation via photocatalysis. The structural and morphological characteristics of the produced catalysts were characterized using various techniques, confirming the successful development of nanocomposite structures of better quality than that of the pure samples. The photocatalytic degradation of antibiotics containing ofloxacin was also investigated. The results suggest that the rGO-ZCS NC outperformed the other composites in terms of photocatalytic activity toward ofloxacin degradation. Superoxide and hydroxyl radicals were the main active species during the degradation process. According to our results, the catalytic activity of rGO-ZCS NC is much better than that of the other composites.

Self-Oxidation Resistance of the Curved Surface of Achromatic Copper.

Copper surfaces that exhibit a wide range of achromatic colors while still metallic have not been studied, despite advancements in antireflection coatings. A series of achromatic copper films grown with [111] preferred orientation by depositing 3D porous nanostructures is introduced via coherent/incoherent atomic sputtering epitaxy. The porous copper nanostructures self-regulate the giant oxidation resistance by constructing a curved surface that generates a series of monoatomic steps, followed by shrinkage of the lattice spacing of one or two surface layers. First-principles calculations confirm that these structural components cooperatively increase the energy barrier against oxygen penetration. The achromaticity of the single-crystalline porous copper films is systematically tuned by geometrical parameters such as pore size distribution and 3D linkage. The optimized achromatic copper films with high oxidation resistance show an unusual switching effect between superhydrophilicity and superhydrophobicity. The tailored 3D porous nanostructures can be a candidate material for numerous applications, such as antireflection coatings, microfluidic devices, droplet tweezers, and reversible wettability switches.

Efficient Integrated Perovskite/Organic Solar Cells via Interdigitated Interfacial Charge Transfer.

The architecture of integrated perovskite/organic solar cells (IPOSCs) is a promising strategy to further enhance the power conversion efficiency (PCE) by extending their photoresponse to the near-infrared range. To maximize the potential benefits of the system, it is crucial to optimize the perovskite crystallinity and intimate morphology of the organic bulk heterojunction (BHJ). More importantly, efficient charge transfer between the interface of the perovskite and BHJ plays a key role in the success of IPOSCs. This paper reports efficient IPOSCs by forming interdigitated interfaces between the perovskite and BHJ layers. Large microscale perovskite grains enable the infiltration of BHJ materials into the perovskite grain boundary, thereby increasing the interface area and promoting efficient charge transfer. Owing to the synergetic effect of the interdigitated interfaces and optimized BHJ nanomorphology, the developed P-I-N-type IPOSC exhibited an excellent PCE of 18.43% with a Jsc of 24.44 mA/cm2, a Voc of 0.95 V, and a FF of 79.49%, which is one of very efficient hybrid perovskite-polymer solar cells.

Thermal Management Enables Stable Perovskite Nanocrystal Light-Emitting Diodes with Novel Hole Transport Material.

The severely insufficient operational lifetime of perovskite light-emitting diodes (LEDs) is incompatible with the rapidly increasing external quantum efficiency, even as it approaches the theoretical limit, thereby significantly impeding the commercialization of perovskite LEDs. In addition, Joule heating induces ion migration and surface defects, degrades the photoluminescence quantum yield and other optoelectronic properties of perovskite films, and induces the crystallization of charge transport layers with low glass transition temperatures, resulting in LED degradation under continuous operation. Here, a novel thermally crosslinked hole transport material, poly(FCA60 -co-BFCA20 -co-VFCA20 ) (poly-FBV), with temperature-dependent hole mobility is designed, which is advantageous for balancing the charge injection of the LEDs and limiting the generation of Joule heating. The optimised CsPbI3 perovskite nanocrystal LEDs with poly-FBV realise approximately a 2-fold external quantum efficiency increase over the LED with commercial hole transport layer poly(4-butyl-phenyl-diphenyl-amine) (poly-TPD), owing to the balanced carrier injection and suppressed exciton quenching. Moreover, because of the Joule heating control provided by the novel crosslinked hole transport material, the LED utilising crosslinked poly-FBV has a 150-fold longer operating lifetime (490 min) than that utilizing poly-TPD (3.3 min). The study opens a new avenue for the use of PNC LEDs in commercial semiconductor optoelectronic devices.

Significant effects of mixed cations on the morphology and photochemical activities of alkali-metal-antimony (Na,K)Sb3O7.

Oxide semiconductors with mixed-valence states generally exhibit excellent optoelectronic and photochemical properties due to facile charge transfer in redox reactions. In this work, we investigate the effects of mixed alkali on the optical absorption, luminescence spectra and photocatalytic abilities of (Na1-xKx)Sb3O7 nanoparticles. All the samples are fabricated using a simple one-step hydrothermal method. The structural studies show that the largest substitution of K+ ions in (Na1-xKx)Sb3O7 is at x = 0.3. In hydrothermal synthesis, the mixed arrangement of K+ and Na+ in (Na1-xKx)Sb3O7 has an influence on the crystal shape of particles. NaSb3O7 develops into a regular cube shape. With the increase of K+ ions in (Na1-xKx)Sb3O7, the edges and corners of the cube are further ground off, resulting in irregularly spherical particles. This mixed-alkali antimonite belongs to a p-type indirect allowed transition semiconductor, and the optical band gap is 2.71 eV (x = 0.3). The intrinsic luminescence of NaSb3O7 is detected at 540 nm, which is nearly quenched in Na0.7K0.3Sb3O7. It is demonstrated that the substitution of K+ in NaSb3O7 significantly increases the photodegradation of RhB solutions. There are two types of Sb cations, i.e., Sb5+ and Sb3+ mixed in the structure. The improved photocatalysis is attributed to the charge mediators between Sb5+/Sb3+ couples. The experiment shows that co-doping cations in antimonite oxides may be one of the strategies to improve photochemical properties.

Intrinsic- and Rare Earth Ion-Activated Luminescence in NbAlO4 with Wide Structure Channels.

Compounds with ordered and interconnected channels have versatile multifunctional applications in technological fields. In this work, we report the intrinsic- and Eu3+-activated luminescence in NbAlO4 with a wide channel structure. NbAlO4 is an n-type semiconductor with an indirect allowed transition and a band-gap energy of 3.26 eV. The conduction band and valence band are composed of Nb 3d and O 2p states, respectively. Unlike the common niobate oxide Nb2O5, NbAlO4 exhibits efficient self-activated luminescence with good thermal stability even at room temperature. The AlO4 tetrahedron effectively blocks the transfer/dispersion of excitation energy between NbO6 chains in NbAlO4, allowing for effective self-activated luminescence from NbO6 activation centers. Moreover, Eu3+-doped NbAlO4 displayed a bright red luminescence of 5D0 → 7F2 transition at 610 nm. The site-selective excitation and luminescence of Eu3+ ions in a spectroscopic probe were utilized to investigate the doping mechanism. It is evidenced that Eu3+ is doped in the structure channel in NbAlO4 lattices, not in the normal cation sites of Nb5+ or Al3+. The experimental findings are valuable in developing new luminescent materials and improving the understanding of the material's channel structure.

Photovoltaic Effects of Dye-Sensitized Solar Cells Using Double-Layered TiO2 Photoelectrodes and Pyrazine-Based Photosensitizers.

In this study, to obtain high performances of the dye-sensitized solar cells using the optimal TiO2 photoelectrode for the synthesized pyrazine-based organic photosensitizers, three types of TiO2 photoelectrodes were fabricated and evaluated for comparison. The double-layered nanoporous TiO2 photoelectrode (SPD type) consisted of a dispersed TiO2 layer and a transparent TiO2 layer. The single-layered nanoporous TiO2 photoelectrodes (D type and SP type) consisted of a dispersed TiO2 layer and a transparent TiO2 layer, respectively. The surface area, pore volume, and crystalline structures of the three types of TiO2 photoelectrodes were analyzed by Brunauer-Emmett-Teller method, field-emission scanning electron microscopy, and X-ray diffractometry to confirm their crystallinity and surface morphology. The structures of the three types of TiO2 photoelectrode-adsorbed organic sensitizers were investigated using X-ray photoelectron spectroscopy. The photovoltaic performances of DSSC devices using three organic photosensitizers adsorbed onto the three types of TiO2 photoelectrodes were investigated under a light intensity of 100 mW/cm2 at AM 1.5. The DSSC device using double-layered SPD type TiO2 photoelectrodes displayed 1.31∼2.64% efficiency, compared to single-layered SP type TiO2 photoelectrodes (1.31∼2.50%) and D type TiO2 photoelectrodes (0.90∼1.54%), using organic photosensitizers. The DSSC device using the SPD type TiO2 photoelectrode and trifluoromethylbenzopyrazine (TPPF) as a photosensitizer showed the highest performances: J sc of 5.69 mA/cm2, V oc of 0.69 V, FF of 0.67, and efficiency of 2.64%. The relationship between photovoltaic effects and interfacial resistance characteristics of DSSCs using the three organic photosensitizers adsorbed onto the three types of TiO2 photoelectrodes could be interpreted from interfacial resistances according to frequency through impedance analysis.

Tailoring the Interface with a Multifunctional Ligand for Highly Efficient and Stable FAPbI3 Perovskite Solar Cells and Modules.

Perovskite solar cells (PeSCs) using FAPbI3 perovskite films often exhibit unfavorable phase transitions and defect-induced nonradiative interfacial recombination, resulting in considerable energy loss and impairing the performance of PeSCs in terms of efficiency, stability, and hysteresis. In this work, a facile interface engineering strategy to control the surface structure and energy-level alignment of perovskite films by tailoring the interface between the FAPbI3 film and hole-transporting layer using 4-hydroxypicolinic acid (4HPA) is reported. According to density functional theory studies, 4HPA has prominent electron delocalization distribution properties that enable it to anchor to the perovskite film surface and facilitate charge transfer at the interface. By enabling multiple bonding interactions with the perovskite layer, including hydrogen bonds, PbO, and PbN dative bonds, 4HPA passivation significantly reduces the trap density and efficiently suppresses nonradiative recombination. The obtained perovskite films exhibit superior optoelectronic properties with improved crystallinity, pure α-phase FAPbI3 , and favorable energy band bending. Following this strategy, 4HPA post-treatment PeSCs achieve a champion power conversion efficiency of 23.28% in 0.12 cm2 cells and 19.26% in 36 cm2 modules with excellent environmental and thermal stabilities.

A Universal Perovskite Nanocrystal Ink for High-Performance Optoelectronic Devices.

Semiconducting lead halide perovskite nanocrystals (PNCs) are regarded as promising candidates for next-generation optoelectronic devices due to their solution processability and outstanding optoelectronic properties. While the field of light-emitting diodes (LEDs) and photovoltaics (PVs), two prime examples of optoelectronic devices, has recently seen a multitude of efforts toward high-performance PNC-based devices, realizing both devices with high efficiencies and stabilities through a single PNC processing strategy has remained a challenge.  In this work, diphenylpropylammonium (DPAI) surface ligands, found through a judicious ab-initio-based ligand search, are shown to provide a solution to this problem. The universal PNC ink with DPAI ligands presented here, prepared through a solution-phase ligand-exchange process, simultaneously allows single-step processed LED and PV devices with peak electroluminescence external quantum efficiency of 17.00% and power conversion efficiency of 14.92% (stabilized output 14.00%), respectively. It is revealed that a careful design of the aromatic rings such as in DPAI is the decisive factor in bestowing such high performances, ease of solution processing, and improved phase stability up to 120 days. This work illustrates the power of ligand design in producing PNC ink formulations for high-throughput production of optoelectronic devices; it also paves a path for "dual-mode" devices with both PV and LED functionalities.

Photovoltaic Performances of Dye-Sensitized Solar Cells Based on Modified Polybutadiene Matrix Electrolytes by Sol-Gel Process.

A new type of polymer matrix electrolyte based on modified polybutadiene (modified PB) was developed for dye-sensitized solar cells (DSSCs) to improve their stability. The modified PB was fabricated by cross-linking the reaction of polybutadiene with siloxane groups as a substitute sol-gel process. A DSSC device using the modified PB matrix electrolyte showed an open-circuit voltage of 0.64 V, a short-circuit current density of 15.00 mA/cm2, and a fill factor of 0.58 under photointensity of 100 mW/cm2 at AM 1.5, consequently leading to an overall solar energy conversion efficiency of 5.49%. The DSSC device using the modified PB matrix electrolyte improved the conductivity, and the charge transfer ability showed the outstanding stability of the device.

Water-Repellent Perovskites Induced by a Blend of Organic Halide Salts for Efficient and Stable Solar Cells.

Despite tremendous progress in the power conversion efficiency (PCE) of perovskite solar cells (PeSCs), the long-term stability issue remains a significant challenge for commercialization. In this study, by blending organic halide salts, phenylethylammonium halide (PEAX, X = I, Br), with CH3NH3PbI3 (MAPbI3), we achieved remarkable enhancements in the water-repellency of perovskite films and long-term stability of PeSCs, together with enhanced PCE. The hydrophobic aromatic PEA+ group in PEAX protects the perovskite film from destruction by water. In addition, the smaller halide Br- in PEABr restructures MAPbI3 to form MAPbI3-xBrx during post-annealing, leading to lattice contraction with beneficial crystallization quality. The perovskite films modified by PEAX exhibited excellent water resistance. When the perovskite films were directly immersed in water, no obvious decompositions were observed, even after 60 s. The PEAX-decorated PeSCs exhibited considerable long-term stability. Under high-humidity conditions (60 ± 5%), the PEAX-decorated PeSCs held 80.5% for PEAI and 85.2% for PEABr of their original PCE after exposure for 100 h, whereas the pristine PeSC device lost more than 99% of its initial PCE after exposure for 60 h under the same conditions. Moreover, compared to the pristine device with a PCE of 13.28%, the PEAX-decorated PeSCs exhibited enhanced PCEs of 17.33% for the PEAI device and 17.18% for the PEABr device.

Enhanced Charge Separation in Ternary Bulk-Heterojunction Organic Solar Cells by Fullerenes.

Carrier generation dynamics in binary PTB7-Th:COi8DFIC (1:1.5) and ternary PTB7-Th:COi8DFIC:PC71BM (1:1.05:0.45) composites were investigated to identify the origins of high power conversion efficiencies (PCEs) in ternary bulk-heterojunction (BHJ) organic solar cells. Steady-state photoluminescence and time-resolved photoinduced absorption spectroscopic analyses revealed that the ternary composite exhibited faster hole transfer from COi8DFIC to PTB7-Th (8 ps compared to 21 ps in the binary composite), which led to an improved exciton separation yield in COi8DFIC (94% compared to 68% in the binary composite). Improved intermixing of the component materials and efficient electron transfer from COi8DFIC to PC71BM facilitated enhancement in the hole transfer rate. The COi8DFIC-to-PC71BM electron transfer promoted an electron transport cascade over PTB7-Th, COi8DFIC, and PC71BM, which efficiently deactivated back-electron transfer (carrier recombination loss) from COi8DFIC to PTB7-Th at ∼160 ps and assisted in improving the PCE of the ternary BHJ cell (13.4% compared to 10.5% in the binary BHJ cell).

Ligand-engineered bandgap stability in mixed-halide perovskite LEDs.

Lead halide perovskites are promising semiconductors for light-emitting applications because they exhibit bright, bandgap-tunable luminescence with high colour purity1,2. Photoluminescence quantum yields close to unity have been achieved for perovskite nanocrystals across a broad range of emission colours, and light-emitting diodes with external quantum efficiencies exceeding 20 per cent-approaching those of commercial organic light-emitting diodes-have been demonstrated in both the infrared and the green emission channels1,3,4. However, owing to the formation of lower-bandgap iodide-rich domains, efficient and colour-stable red electroluminescence from mixed-halide perovskites has not yet been realized5,6. Here we report the treatment of mixed-halide perovskite nanocrystals with multidentate ligands to suppress halide segregation under electroluminescent operation. We demonstrate colour-stable, red emission centred at 620 nanometres, with an electroluminescence external quantum efficiency of 20.3 per cent. We show that a key function of the ligand treatment is to 'clean' the nanocrystal surface through the removal of lead atoms. Density functional theory calculations reveal that the binding between the ligands and the nanocrystal surface suppresses the formation of iodine Frenkel defects, which in turn inhibits halide segregation. Our work exemplifies how the functionality of metal halide perovskites is extremely sensitive to the nature of the (nano)crystalline surface and presents a route through which to control the formation and migration of surface defects. This is critical to achieve bandgap stability for light emission and could also have a broader impact on other optoelectronic applications-such as photovoltaics-for which bandgap stability is required.

Carrier losses in non-geminate charge-transferred states of nonfullerene acceptor-based organic solar cells.

To understand the current limitations of nonfullerene-based organic solar cells (OSCs), the early-time dynamics of the carrier generation in the high performance bulk heterojunction (BHJ) blend of a semiconducting polymer, PBDB-T, and the low bandgap nonfullerene acceptor, ITIC-m, are investigated. After photoexcitation, photo-induced excitons are separated through the ultrafast (~200 fs) electron transfer process from PBDB-T to ITIC-m and through the fast (3-6 ps) hole transfer process from ITIC-m to PBDB-T. However, a part of the separated charges recombines in the non-geminate (long-range) charge-transferred (CT) states. The yield of mobile carriers is correspondingly decreased by recombination in the CT states. In our measurements, the carrier recombination loss in the CT state is decreased by optimizing the BHJ morphology, especially for showing better electron mobility using a processing additive (1,8-diiodooctane) during the fabrication of the composite film, as evidenced by the decreased CT band intensity at ~30 ps and the increased polaron band intensity, which eventually improve power conversion efficiencies (PCEs).

Bilateral Interface Engineering for Efficient and Stable Perovskite Solar Cells Using Phenylethylammonium Iodide.

Achieving high efficiency and long-term device stability is a vital issue for the commercialization of organic-inorganic hybrid perovskite solar cells (PeSCs). In this work, phenylethylammonium iodide (PEAI)-induced bilateral interface engineering was developed to improve the device efficiency and stability of methylammonium lead triiodide (MAPbI3)-based PeSCs. Introducing PEAI onto a poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) layer modifies the surface properties of PEDOT:PSS and facilitates the formation of a high-quality perovskite active layer with enlarged grains on PEDOT:PSS. PEA+ in PEAI-PEDOT:PSS also alters the work function of PEDOT:PSS, leading to a reduction in the energy difference between the PEDOT:PSS and MAPbI3 perovskite layers, which decreases the energy loss during charge transfer. Additionally, depositing PEAI onto three-dimensional (3D) perovskite yields a two-dimensional/three-dimensional (2D/3D) stacked structure for the perovskite active layer. Because the two-dimensional (2D) top layer acts as a capping layer to prevent water penetration, the stability of the perovskite active layer is significantly enhanced. A PeSC device fabricated based on this combination exhibits enhanced power conversion efficiency (PCE) and an extended device lifetime compared to a pristine PeSC. Under high-humidity conditions (75 ± 5%), the PEAI-treated PeSC retains 88% of its initial power conversion efficiency (PCE) after 100 h. In contrast, a pristine PeSC device loses over 99% of its initial PCE after only 25 h under the same conditions.

Lead Acetate Assisted Interface Engineering for Highly Efficient and Stable Perovskite Solar Cells.

High power conversion efficiency (PCE) and long-term stability are inevitable issues faced in practical device applications of perovskite solar cells. In this paper, significant enhancements in the device efficiency and stability are achieved by using a surface-active lead acetate (Pb(OAc)2) at the top or bottom of CH3NH3PbI3 (MAPbI3)-based perovskite. When a saturated Pb(OAc)2 solution is introduced on the top of the MAPbI3 perovskite precursor, the OAc- in Pb(OAc)2 participates in lattice restructuring of MAPbI3 to form MAPbI3-x(OAc)x, thereby producing a high-quality perovskite film with high crystallinity, large grain sizes, and uniform and pinhole-free morphology. Moreover, when Pb(OAc)2 solution is mixed in the poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS) solution in the bottom way, the OAc- in Pb(OAc)2 improves the water resistance of PEDOT-PSS. As the OAc- easily bonds with the Pb2+, the deposition of MAPbI3 precursor onto the Pb(OAc)2 mixed with PEDOT-PSS results in a reduction of the uncoordinated Pb, leading to strong stabilization of the perovskite layer. Both the top- and bottom-treated devices exhibit enhanced PCE values of 18.93% and 18.28%, respectively, compared to the conventional device with a PCE of 16.47%, which originates from decreased trap sites and reduced energy barriers. In particular, the bottom-treated device exhibits long-term stability, with more than 84% of its initial PCE over 800 h in an ambient environment.

One-Pot Exfoliation of Graphitic C3 N4 Quantum Dots for Blue QLEDs by Methylamine Intercalation.

Here, a simplified synthesis of graphitic carbon nitride quantum dots (g-C3 N4 -QDs) with improved solution and electroluminescent properties using a one-pot methylamine intercalation-stripping method (OMIM) to hydrothermally exfoliate QDs from bulk graphitic carbon nitride (g-C3 N4 ) is presented. The quantum dots synthesized by this method retain the blue photoluminescence with extremely high fluorescent quantum yield (47.0%). As compared to previously reported quantum dots, the g-C3 N4 -QDs synthesized herein have lower polydispersity and improved solution stability due to high absolute zeta-potential (-41.23 mV), which combine to create a much more tractable material for solution processed thin film fabrication. Spin coating of these QDs yields uniform films with full coverage and low surface roughness ideal for quantum dot light-emitting diode (QLED) fabrication. When incorporated into a functional QLED with OMIM g-C3 N4 -QDs as the emitting layer, the LED demonstrates ≈60× higher luminance (605 vs 11 Cd m-2 ) at lower operating voltage (9 vs 21 V), as compared to the previously reported first generation g-C3 N4 QLEDs, though further work is needed to improve device stability.

Infrared excited Er3+/Yb3+ codoped NaLaMgWO6 phosphors with intense green up-conversion luminescence and excellent temperature sensing performance.

The Er3+/Yb3+-codoped NaLaMgWO6 phosphors were synthesized via a traditional high-temperature solid-state reaction method. The temperature sensing performance was thoroughly investigated by studying the temperature-dependent up-conversion (UC) emission intensity ratio in the range of 293-533 K. A remarkable enhancement of green UC emission, as well as enhanced temperature sensitivity, were observed by increasing the Yb3+ concentration. The maximum absolute sensor sensitivity was 2.29% K-1 at 533 K. When the pump power of the 980 nm laser increased from 200 to 1000 mW, a slightly elevated temperature from 293-307 K was achieved in the compounds. Using the prepared phosphors and a 940 nm NIR chip, a green-emitting LED device was developed to confirm the applicability of our prepared phosphors for solid-state lighting. As a temperature probe, the prepared phosphor detected that the temperature increased from 286 K to 315 K when the drive current was increased from 90 mA to 300 mA. These results suggest that the Er3+/Yb3+-codoped NaLaMgWO6 phosphors have a potential application in solid-state lighting and optical thermometry.