Energy Transfer Channel Research Articles

Quantum–Chemical Study of the Photophysical Behavior of Mesogenic Europium(III) Complexes with β‐Diketones and Lewis Bases

AbstractMetal‐containing liquid crystals such as Ln(III) complexes possess unique structural, liquid‐crystalline (LC), optical, and magnetic properties and represent modern cutting‐edge multifunctional materials. Application of mesogenic Ln(III) complexes is hindered by their nontrivial structure–property relationships. These relationships, in turn, depend on various factors, including insufficiently studied physicochemical processes. Although a proper Ln(III) element and the respective ligand environment are selected prior to synthesis of such complexes, the structural features of the coordination polyhedra, especially upon photoexcitation, are not uniquely defined. Therefore, this work focuses on the development of theoretical approaches to creating multifunctional materials represented by highly luminescent mesogenic Eu(III) complexes with β‐diketones and Lewis bases. The relationships between their structure, the parameters of Voronoi–Dirichlet polyhedra, the luminescence efficiency, and the LC properties were considered. The calculated excited states and intramolecular energy transfer rates were used to determine intramolecular energy transfer channels. The LC behavior of the studied materials was shown to mainly depend on the ligand environment, whereas their optical properties were found to be mostly governed by the coordination polyhedra.

La3Sc2Ga3O12:Cr3+, Nd3+ near-infrared phosphor for nondestructive detection and luminescence thermometry

To develop continuous broadband emission near-infrared (NIR) phosphors compatible with blue LED chips, numerous Cr3+-Yb3+ co-doped phosphors have been synthesized. However, the emission spectra of Cr3+ vary significantly across different matrix materials, while Yb3+ maintains a relatively stable emission spectrum. This variation leads to notable luminescence depressions between 850 and 900 nm in many Cr3+-Yb3+ co-doped phosphors. To address this emission spectrum gap, we utilized Cr3+ as a sensitizer and introduced Nd3+ as the luminescence center within the La3Sc2Ga3O12 matrix material, establishing a Cr3+-Nd3+ energy transfer channel. Under 480 nm excitation, we tuned emission peaks at 800 nm (Cr3+) and 881 nm (Nd3+). The stable NIR emission of Nd3+ effectively compensates for the missing spectrum in Cr3+-Yb3+ co-doping. The Cr3+-Nd3+ energy transfer process was thoroughly analyzed using diffuse reflection spectrum, excitation spectrum, and fluorescence decay curves. The LSGO:0.125Cr3+, 0.03Nd3+ compound with the best optical performance was packaged with a 480 nm LED chip to create a NIR light source. At a working current of 10 mA, it achieved a photoelectric conversion efficiency of 9.45 %, demonstrating its potential for applications in non-destructive detection and luminescence thermometry. This work presents a novel strategy for tuning NIR spectral distribution and developing continuous broadband NIR phosphors.

A Single‐Component Sb/Ho: Cs2Na0.9Ag0.1(In/Bi)Cl6 White Phosphor with a Record Color Rendering Index of 97.4

AbstractThe study on phosphors‐converted white light‐emitting diodes (pc‐WLEDs) using lead‐free double perovskites (DPs) as single‐component white phosphors is widely concerned. However, the photoluminescence quantum yields (PLQY) of white luminescence and color rendering index (CRI) of WLED are not satisfactory. Herein, a new Sb/Ho: Cs2Na0.9Ag0.1(In/Bi)Cl6 single‐component white phosphor with the highest PLQY of 93% and a record CRI of 97.4 is reported. Experimental data and theoretical calculations evidence that in addition to broadband yellow emission of the self‐trapped exciton (STE) recombination, the material also exhibits blue emission from Sb3+: 3P1→1S0 transition and red one assigned to Ho3+: 5F5→5I8 transition. Steady‐state and time‐resolved PL spectra verify the existence of two energy transfer channels from both Sb3+ and STE to Ho3+ dopants. As a demo, Sb/Ho: Cs2Na0.9Ag0.1(In/Bi) Cl6‐based WLED is constructed, showing excellent comprehensive optical performance with specially improved saturation red index R9 and blue one R12. This work provides a novel single‐component rare‐earth doped DP white phosphor for high CRI full‐spectrum solid‐state lighting.

Highly efficient detection of aspirin using novel lanthanide-xanthan gum hydrogels

A commonly employed method for identifying aspirin involves the use of either HPLC or electrochemical analysis. In this article, a highly selective and ultrasensitive fluorescent sensor with convenient synthesis steps for the detection of aspirin was reported. This study introduced a novel hybrid organic-inorganic optical network hydrogel achieved through the integration of a complex of Tb-xanthan gum (XG) into the backbone of polyvinyl alcohol (PVA). This hydrogel fabricated in a water-based environment, exhibits weak green luminescence at the beginning owing to the chelation and sensitization of lanthanide (Tb3+) ions by ligands. Interestingly, the green emission intensity observed at λ ex = 346 nm, is enhanced by dual energy-transfer channels from XG and aspirin. We experimentally demonstrate that luminescent Tb3+-XG complex-binding aptamer hydrogels can selectively detect aspirin from 250 nM to 1 μM with a detection limit of 150 nM in this study. Furthermore, we discuss the resulting structure, thermal stability, excellent swelling properties, mechanical characteristics, and morphology of this light-emission material in detail. The success of this method will open up new opportunities for the use of hydrogels in visual fluorescence sensing applications.

Analyses of nonequilibrium transport in atmospheric-pressure direct-current argon discharge under different modes

Abstract The key plasma parameters under different discharge modes, such as heavy-particle and electron temperatures, electron number density, and nonequilibrium volume of plasmas, play important roles in various applications of gas discharge plasmas. In this study, a self-consistent two-dimensional nonequilibrium fluid model coupled with an external circuit model is established to reveal the mechanisms related to the discharge modes, including the normal glow, abnormal glow, arc, and glow-to-arc transition modes, with an atmospheric-pressure direct-current (DC) argon discharge as a model plasma system. The modeling results show that, under different discharge modes, the most significant difference between the preceding four discharge modes lies in the current and energy transfer processes on the cathode side. On one hand, the current to the cathode surface is mainly delivered by the ions coming from the plasma column under the glow discharge mode due to the low temperature of the solid cathode, whereas the thermionic and secondary electrons emitted from the hot cathode surface play a very important role under the arc mode with a higher cathode surface temperature and higher ion flux toward the cathode. On the other hand, the energy transfer channel on the cathode side changes from mainly heating the solid cathode under the glow mode to simultaneously heating both the solid cathode and plasma column under the arc mode with an increase in the discharge current. Consequently, the power density in the cathode sheath (P c) was used as a key parameter for judging different discharge modes, and the range of (0.28–1.2) × 1012 W m−3 was determined as a critical window of P c corresponding to the glow-to-arc-mode transition for the atmospheric-pressure DC argon discharge, which was also verified by comparison with the experimental results in this study and the data in the previous literature.

A Scalable, Wide-Angle Metasurface Array for Electromagnetic Energy Harvesting.

A metasurface array for electromagnetic (EM) energy harvesting for Wi-Fi bands is presented in this paper; the metasurface array consists of a metasurface unit, a rectifier, and a load resistor. Each row of unit cells in the array is interconnected to form an energy transfer channel, which enables the transfer and concentration of incident power. Furthermore, at the terminal of the channel, a single series diode rectifier circuit and a load resistor are integrated in a coplanar manner. It is used to rectify the energy in Wi-Fi bands and enables DC energy harvesting across the load. Finally, a 5 × 7 prototype of the metasurface array is fabricated and measured for the verification of the rationality of the design. Testing in an anechoic chamber shows that the prototype achieves a 72% RF-DC efficiency at 5.9 GHz when the available incident power is about 7 dBm.

Tunable optical properties of isoreticular UiO-67 MOFs for photocatalysis: a theoretical study.

A theoretical study of the reported photocatalytic systems based on Zr-based MOF (UiO-67) with biphenyl-4,4'-dicarboxylic acid (bpdc) and 2,2'-bipyridine-5,5'-dicarboxylic acid (bpydc) as linkers was performed. Quantum chemical calculations were carried out to understand the optical properties of the materials and to facilitate the rational design of new UiO-67 derivatives with potentially improved features as photocatalysts under ambient conditions. Hence, the effect of the structural modifications on the optical properties was studied considering different designs based on the nature of the linkers: in 1 only the bpdc linker was considered, or the mixture 1 : 1 between bpdc and bpydc linkers (labeled as 1A). Also, substituents R, -NH2, and -SH, were included in the 1A MOF only over the bpdc linker (labeled as 1A-bpdc-R) and on both bpdc and bpydc linkers (labeled as 1A-R). Thus a family of six isoreticular UiO-67 derivatives was theoretically characterized using Density Functional Theory (DFT) calculations on the ground singlet (S0) and first excited states (singlet and triplet) using Time-Dependent Density Functional Theory (TD-DFT), multiconfigurational post-Hartree-Fock method via Complete Active Space Self-Consistent Field (CASSCF). In addition, the use of periodic DFT calculations suggest that the energy transfer (ET) channel between bpdc and bpydc linkers might generate more luminescence quenching of 1A when compare to 1. Besides, the results suggest that the 1A-R (R: -SH and NH2) can be used under ambient conditions; however, the ET exhibited by 1A, cannot take place in the same magnitude in these systems. These ET can favor the photocatalytic reduction of a potential metal ion, that can coordinate with the bpydc ligand, via LMCT transition. Consequently, the MOF might be photocatalytically active against molecules of interest (such as H2, N2, CO2, among others) with photo-reduced metal ions. These theoretical results serve as a useful tool to guide experimental efforts in the design of new photocatalytic MOF-based systems.

Thermal Enhanced Energy Transfer and High Thermal Sensitivity of Sb3+ Doped Cs2KYbCl6 Rare Earth Double Perovskites

AbstractRare‐earth based double perovskites (DPs) have attracted much attention due to stable, efficient, and unique luminescence, and wide applications in many optoelectronic fields. However, their weak near‐infrared (NIR) emission and poor anti‐thermal quenching severely limit the further applications. Herein, Sb3+‐doped Cs2KYbCl6 DP with cyan self‐trapped exciton (STE) and NIR emission is prepared by a solvothermal method, and the separate photoluminescence quantum yields from STE and NIR emission reached ≈26.1% and 43.8%, respectively. More importantly, Sb3+ not only contributes to the absorption and energy transfer but also helps to establish an effective thermally enhanced energy transfer channel through self‐trapping state, resulting in the NIR emission with superior anti‐thermal quenching resistance. The thermal sensitivity of luminescence intensity ratio (LIR) of I1010 nm/I505 nm (I is the intensity of PL) and time‐resolved temperature sensor reach 21.4 and 13.6% K−1, respectively, which are ahead of most temperature sensing materials. Furthermore, it is found that the material exhibited advanced multifunctional applications in LED lighting, flexible luminescent thin film, and NIR imaging. This work provides in‐depth understanding on photophysical mechanisms of rare‐earth luminescent materials and references for designing high‐performance materials.

Resonance of Low-frequency Electromagnetic and Ion-sound Modes in the Solar Wind

Parker Solar Probe measurements have recently shown that coherent fast magnetosonic and Alfvén ion-cyclotron waves are abundant in the solar wind and can be accompanied by higher-frequency electrostatic fluctuations. In this Letter we reveal the nonlinear process capable of channelling the energy of low-frequency electromagnetic to higher-frequency electrostatic fluctuations observed on board Parker Solar Probe. We present Hall-MHD simulations demonstrating that low-frequency electromagnetic fluctuations can resonate with the ion-sound mode, which results in steepening of plasma density fluctuations, electrostatic spikes, and harmonics in the electric field spectrum. The resonance can occur around the wavenumber determined by the ratio between local sound and Alfvén speeds, but only in the case of oblique propagation to the background magnetic field. The resonance wavenumber, its width, and steepening timescale are estimated, and all indicate that the revealed two-wave resonance can frequently occur in the solar wind. This process can be a potential channel of energy transfer from cyclotron resonant ions producing the electromagnetic fluctuations to Landau resonant ions and electrons absorbing the energy of the higher-frequency electrostatic fluctuations.

Efficient and tunable white light emitting from Sb3+, Tb3+, and Sm3+ Co-doped Cs2NaInCl6 double perovskite via multiple energy transfer processes

Inorganic lead-free double perovskites have the advantages of low toxicity, broadband emission, and good stability, which make them promising luminescent materials for lighting applications. However, due to the limited regulation of their self-trapped exciton emission, it is still greatly challenging to achieve white light emitting from a single double perovskite host. Herein, efficient and tunable white light is realized in Cs2NaInCl6: Sb3+, Tb3+, Sm3+ double perovskite by controlling the ratios of the doped three ions with blue, green, and red emissions, respectively. The steady-state and transient fluorescence spectra of singly- and doubly-doped double perovskites reveal the existence of multiple energy transfer channels in the triply-doped phosphors, including from Sb3+ to Tb3+, Sb3+ to Sm3+, and Tb3+ to Sm3+. Benefiting from these channels, the color coordinates of the triply-doped phosphors can cross the whole white light area of the CIE chromaticity diagram by adjusting the ratios of the three dopants, and the maximum internal quantum yield of the white light phosphors is 66.61 %. The white emission phosphors show the characteristic of being independent of excitation wavelength within 310–360 nm. Furthermore, the emission intensity at 430 K of the white light phosphor Cs2NaInCl6: 0.01Sb3+, 0.65Tb3+, 0.20Sm3+ remains 50 % of that at room temperature. A WLED device fabricated with the phosphor and a 365 nm LED chip exhibits a high color rendering index of 90.9, correlated color temperature of 5469 K, and CIE coordinates of (0.333 and 0.328). The results indicate that the as-prepared double perovskite materials are promising candidates in the solid-state lighting field.

Harvesting Hot Excitons for High‐Efficiency OLEDs with Extremely Low‐Efficiency Roll‐Off via Utilizing the Cascade Exciton Energy Transfer from Host and Sensitizer to Emitter

AbstractAlthough high‐efficiency host‐sensitizer‐TBRb‐based organic light‐emitting diodes (HST‐OLEDs) are widely reported, the reasons for their high performances are still vague because the important role of hot exciton in TBRb emitter (T2, TBRb) has not been recognized previously. Herein, a maximum external quantum efficiency (EQE) of 24.9% is obtained from a HST‐OLED by co‐doping the Ir(ppy)3 sensitizer and TBRb emitter into the CBP host. Such a remarkable efficiency is mainly attributed to the efficient utilization of the T2, TBRb via the cascade Dexter energy transfer (DET) channels from triplet excitons of host and sensitizer to T2, TBRb (T1, CBP T1, Ir(ppy)3 T2, TBRb) followed by the hot‐exciton reverse intersystem crossing (RISC, T2, TBRb S1, TBRb) and triplet fusion (TF, T2, TBRb + T2, TBRb Sm, TBRb S1, TBRb) processes for radiative decays. These cascade DET channels are demonstrated by spectroscopic analyses and magneto‐electroluminescence studies. More importantly, this HST‐OLED presents an extremely low‐efficiency roll‐off, that is, the EQEs separately exhibit 24.34% and 19.73% at 1000 and 10 000 cd m−2 compared to the maximum EQE of 24.9%. Obviously, this work paves a promising pathway for fabricating further high‐efficiency HST‐OLEDs for applications in illumination and flat‐panel display.

Breakthrough Boost of Stokes Fluorescence from Er3+ in Perovskites for Flexible Temperature Sensing

AbstractPerovskites with ultra‐low phonon energy have excellent radiation properties, while the population distribution of its luminescent initial state needs to be facilitated to further optimize the stokes fluorescence of Er3+ under high‐energy photons excitation. Herein, UV excitability of Er3+ is remodeled by building an energy transfer channel from Sb3+ to Er3+ in Cs2NaInCl6 (CNIC) microcrystal to realize the enhancement of stokes fluorescence of Er3+. Under UV excitation, the breakthrough boost of Er3+ is observed in Cs2NaInCl6:Sb3+‐Er3+ (CNIC:Sb‐Er), and the sensitization coefficient from Sb3+ to Er3+ in CNIC is derived to be as high as 112. Moreover, CNIC:Sb‐Er is embedded into functional fibers to enhance the crystal stability and the composite flexibility, which form fluorescence fibers with strong radiation transition probability. Finally, a high‐precision temperature sensing is achieved based on FIR (fluorescence intensity ratios) technology, and the maximum relative sensitivities of CNIC:Sb‐Er phosphors and CNIC:Sb‐Er/PAN fibers reach 1.13 and 1.10% K−1, respectively, indicating that CNIC:Sb‐Er and CNIC:Sb‐Er/PAN fibers have potential applications in optical temperature sensors.

Tuneable Efficient White Emission of Sb3+/Mn2+ Co-Doped Lead-Free Perovskites for Single-Component White Light-Emitting Diodes.

Inorganic lead-free perovskite nanocrystals (NCs) with broadband self-trapped exciton (STEs) emission and low toxicity have shown enormous application prospects in the field of display and lighting. However, white light-emitting diodes (WLEDs) based on a single-component material with high photoluminescence quantum yield (PLQY) remain challenging. Here, we demonstrate a novel codoping strategy by introducing Sb3+/Mn2+ ions to achieve the tuneable dual emission in lead-free perovskite Cs3InCl6 NCs. The PLQY increases to 59.64% after doping with Sb3+. The codoped Cs3InCl6 NCs exhibit efficient white light emission due to the energy transfer channel from STEs to Mn2+ ions with PLQY of 51.38%. Density functional theory (DFT) calculations have been used to verify deeply the effects of Sb3+/Mn2+ doping. WLEDs based on Sb3+/Mn2+-codoped Cs3InCl6 NCs are explored with color rendering index of 85.5 and color coordinate of (0.398, 0.445), which have been successfully applied as photodetector lighting sources. This work provides a new perspective for designing novel lead-free perovskites to achieve single-component WLEDs.

Direct observation of room-temperature high-level triplet–triplet annihilation process in 1%rubrene-doped OLEDs with a CzDBA sensitizer

Using the magneto-electroluminescence as a sensitive and fingerprint probing tool, a “hot exciton” channel, named the high-level triplet–triplet annihilation (HL-TTA or T2T2A, T2 + T2 → Sn → S1 → S0 + hv) process from the high-lying triplet (T2) to the lowest singlet states, is observed in 1%rubrene-doped organic light-emitting diodes with a thermally activated delayed fluorescence sensitizer of 9,10-bis(4-(9H-carbazol-9-yl)-2,6-dimethylphenyl)-9,10-diboraanthracene (CzDBA) at room temperature. The addition of a sensitizer simultaneously promotes the Dexter energy transfer channels of host-sensitizer and sensitizer-guest triplets, thereby increasing the amounts of T2 states and inducing the occurrence of the HL-TTA process. Additionally, the HL-TTA enhances with the increase in the bias current and decreases with lowering the working temperature, which is consistent with the current dependence of the conventional low-level TTA (T1T1A, T1 + T1 → S1 + S0) process but contrary to its temperature dependence. More interestingly, the high concentration of CzDBA induces the H-type aggregation of rubrene molecules, promoting the singlet fission process but suppressing the HL-TTA process. These findings enrich the physical understanding of hot exciton channels and provide ideas for the preparation of high-performance devices.

Sb/X (X = Mn, Er, Ho) Co‐Doped Lead‐Free Double Perovskite Cs2NaInCl6 for Single‐Component White Light Emission

AbstractRecently, the incorporation of transition‐metal ions into lead‐free double perovskite has garnered considerable attention for improving the lattice environment and enhancing photoluminescence (PL) to achieve white light emission. Here, Sb/X (Mn, Er, Ho) co‐doped Cs2NaInCl6 (CNIC) microcrystals (MCs) synthesized by conventional hydrothermal method are developed for single‐component white light emission with various photoinduced transition mechanisms. Sb doping in CNIC MCs causes the breaking of non‐parity forbidden transition under 360 nm laser excitation and results in blue emission; Sb/X co‐doping for CNIC MCs successfully broadens the spectrum with multi‐peak emission, which consists of unique X‐peak emission and blue emission peaked at 445 nm. The energy transfer channels from both free excitons state of CNIC and self‐trapping excitons (STEs) state of [SbCl6]3− to X ion are proved and studied by use of steady‐state and time‐resolved PL spectroscopy. Among them, Sb/Er co‐doped CNIC MCs show unique dual‐mode PL under 360 and 980 nm laser excitation. Single‐component white light emitting diode is successfully fabricated by adjusting the composition of Sb/X co‐doped CNIC MCs, which provides an alternative path for realizing single‐component white light illumination.

Multiwavelength Excitation in Ho3+-Doped All-Inorganic Double Perovskites Achieved by Codoping Mn2+ for Warm-White LEDs and Plant Growth.

Doping lanthanide ions is an efficient method to modify the optical properties of lead-free double-perovskite halides. However, most lanthanide-doped double perovskites show a low luminescence efficiency and require a high excitation energy. Here, we have successfully prepared a series of Ho3+-doped Cs2NaBiCl6 microcrystals through a simple hydrothermal method and obtained strong characteristic emissions of Ho3+ at 492 and 657 nm under low-energy excitation (449 nm). After codoping Mn2+, apart from the characteristic emissions from Ho3+ under 450 nm wavelength excitation, the orangish-red luminescence consisting of the emission band centered at 591 nm from Mn2+ and a sharp emission peak at 657 nm from Ho3+ is obtained under 355 nm UV light excitation. Photoluminescence (PL) emission and excitation spectra, along with the PL decay curves, confirm the existence of an energy-transfer channel from Cs2NaBiCl6 to Mn2+ and then from Mn2+ to Ho3+. The enhanced absorption efficiency (10.5 → 70.7%) suggests that the codoping of Mn2+ overcomes the low absorption efficiency caused by f-f forbidden transitions of Ho3+. Finally, the diverse luminescent performance within the Cs2NaBiCl6:Ho3+, Mn2+ phosphor is realized by altering the excitation wavelength, thereby enabling its application in warm-white-light-emitting diodes and plant growth in this work.

Lattice doping of lanthanide ions in Cs2ZrCl6 nanocrystals enabling phase transition and tunable photoluminescence.

Dopants can endow lead-free perovskite nanocrystals with novel photoelectric properties. However, understanding the effect of dopants on the structure and energy transfer of lead-free perovskite nanocrystals remains limited. In this work, we synthesize zero-dimensional Cs2ZrCl6 nanocrystals with a blue light quantum yield of up to 75.6% by an improved hot-injection method. And we introduce trace amounts of lanthanide ions (Ln3+) (<∼8%) in the lattice of nanocrystals and establish an effective energy transfer channel from self-trapped excitons (STEs) to various Ln3+ ions (Tb3+, Eu3+, Dy3+, Sm3+, and Pr3+), which can achieve tunable photoluminescence between red, green and blue. Interestingly, with increasing Ln3+ concentrations (>∼10%), the phase transition from the cubic phase Cs2ZrCl6:Ln3+ to the monoclinic phase Cs3LnCl6:Zr4+ occurred, while Zr4+ ions began to act as dopants. And a new energy transfer channel from dopant [ZrCl6]2- to host Ln3+ ions was established in the Cs3LnCl6 host accompanied by enhanced broadband photoluminescence excitation (PLE) and photoluminescence (PL). In particular, the photoluminescence quantum yield (PLQY) of Tb3+ ions increases from 0.77% to 54% upon the phase transition (under 276 nm excitation). Our study provides new insights into the effects of dopants on the structure of perovskite nanocrystals and is beneficial to the design of a variety of light-emitting materials for optoelectronic applications.

Temperature sensing performance of Er3+:Yb3+ co-doped CaF2 ceramic powders using near-infrared light

Luminescent materials for application in temperature sensing have caught a lot of interest in recent years. Particularly erbium (Er3+)-doped fluoride-based materials (EFM), which are readily accessible by near-infrared (NIR) excitation to produce efficient photon conversion. It has been established that ytterbium (Yb3+) may improve the performance of EFMs in both bulk and nanostructured forms by energy transfer channels among rare-earth ions in interstitial clusters. In this work, a comprehensive analysis of the Er3+:Yb3+:CaF2 crystalline structure, photoluminescence, and energy transfer from Yb3+ to Er3+ is presented for powders prepared by combustion synthesis. The Er3+:Yb3+:CaF2 powders display exceptional photon down-shift and up-conversion when exposed to NIR light (λ = 975 nm). The luminescence spectral change of the NIR emission around 1.5 μm, which corresponds to the Er3+ electronic transition 4I13/2 → 4I15/2, was investigated in a temperature range of 298–423 K for application in temperature sensing of biological systems exploring the third biological window. The luminescence intensity ratio technique was applied to the thermally coupled Stark sublevels of states 4I13/2 and 4I15/2 with the highest estimated temperature relative sensitivity being around 0.4 %/K at 298 K.

Correction: Construction of energy transfer channels from [SbCl6]3− to Ln3+ (Ln3+ = Ho3+, Er3+) in Cs2NaGdCl6 for advanced anti-counterfeiting materials

Correction for ‘Construction of energy transfer channels from [SbCl6]3− to Ln3+ (Ln3+ = Ho3+, Er3+) in Cs2NaGdCl6 for advanced anti-counterfeiting materials’ by Yanyang Li et al., J. Mater. Chem. C, 2024, 12, 12589–12597, https://doi.org/10.1039/D4TC02186J.

Construction of energy transfer channels from [SbCl6]3− to Ln3+ (Ln3+ = Ho3+, Er3+) in Cs2NaGdCl6 for advanced anti-counterfeiting materials

Construction of energy transfer channels from [SbCl6]3− to Ln3+ (Ln3+ = Ho3+, Er3+) in CNGC opens up new possibilities for high security anti-counterfeiting applications.