Photoluminescence Quantum Efficiency Research Articles

Enhanced photoluminescence characteristics in Mg doped Alq3: An insight into doping mechanism

The present paper deals with the investigations on the effect of Mg doping on the structural and photophysical properties of Alq3 thin films. Mg doped Alq3 powders, with varying Mg concentrations, are synthesized using co-precipitation method and their thin films are deposited using vacuum evaporation method. These films are subjected to different analytical analyses to study the effect of Mg doping on the structural and photophysical properties of Alq3. It has been observed that Mg is attached at the central part of the Alq3 molecules making bonds with Al, N and O atoms. In this process, Mg atoms transfer electrons to Alq3 molecules and increases the electron density in its highest occupied molecular orbital (HOMO). Increased HOMO electron density in Mg doped Alq3 results in the improvement in its photoluminescence characteristics. Highest photoluminescent characteristics are observed for Mg doped Alq3 having 1.5 % (by mole) Mg which shows almost 2-fold enhancement in photoluminescence quantum efficiency (PLQY) and 3-fold enhancement in radiative decay rate. The results obtained in this work suggest that Mg doped Alq3 films may be integrated in high performing organic light emitting devices.

Intramolecular Hydrogen Bonding Rigidifying Flexible Bridge for Solution- and Vacuum-Processed TSCT-TADF Emitters.

To realize strong donor-acceptor face-to-face stacking for efficient through-space charge transfer-type thermally activated delayed fluorescence, a conceptually new design strategy is proposed to couple flexible bridges with adequate rigidity via built-in intramolecular hydrogen bonds (IHBs). The resulting emitter ACE-CN has a planarized benzyl methyl ether bridge self-anchored by the C-H···O IHB and shows a high photoluminescence quantum efficiency of 93%. The solution- and vacuum-processed devices exhibited high external quantum efficiencies of 11.8% and 24.7%, respectively.

Steric Control of Luminescence in Phenyl-Substituted Trityl Radicals.

Triphenylmethyl (trityl) radicals have shown potential for use in organic optoelectronic applications, but the design of practical trityl structures has been limited to donor/radical charge-transfer systems due to the poor luminescence of alternant symmetry hydrocarbons. Here, we circumvent the symmetry-forbidden transition of alternant hydrocarbons via excited-state symmetry breaking in a series of phenyl-substituted tris(2,4,6-trichlorophenyl)methyl (TTM) radicals. We show that 3-fold phenyl substitution enhances the emission of the TTM radical and that steric control modulates the optical properties in these systems. Simple ortho-methylphenyl substitution boosts the photoluminescence quantum efficiency from 1% (for TTM) to 65% at a peak wavelength of 612 nm (for 2-T3TTM) in solution. In the crystalline solid state, the neat 2-T3TTM radical shows a remarkably high photoluminescence quantum efficiency of 25% for emission peaking at 706 nm. This has implications in the design of aryl-substituted radical structures where the electronic coupling of the substituents influences variables such as emission, charge transfer, and spin interaction.

Role of surface treatments and localized surface plasmon nanoparticles on internal quantum efficiency of 800 nm diameter blue GaN/InGaN nano light emitting diodes

Arrays of nanorod multi-quantum-well (MQW) blue light emitting diodes (nLEDs) with diameter 800 nm were prepared by reactive ion etching (RIE) with subsequent surface treatment by KOH etching alone, and KOH etching followed by SiO2 passivation with the SiO2 prepared by the sol-gel technique. In addition, the effects of Ag/SiO2 core/shell nanoparticles prepared by sol-gel were studied for all surface treatments. For as etched nLEDs, the Internal Quantum Efficiency (IQE) of photoluminescence was low, 5.5 %, because of the impact of surface damage introduced by RIE. KOH etching and KOH plus SiO2 passivation produced an increase of IQE to respectively 5.7 and 6.8 %. When the Ag/SiO2 core/shell nanoparticles known to produce localized surface plasmon resonance at the wavelength well-matched to the light emission from the MQWs were added to the polymer filling the gaps between the MQW nanorods, the result was found to depend on finding a proper balance between the enhancement due to the interaction Ag/SiO2 nanoparticles adjacent to the MQW nanorods and the absorption by “idle” Ag/SiO2 particles in the bulk of the polymer. When optimal concentrations of LSP NPs giving rise to maximal enhancement of the MQW PL intensity were used, a considerable improvement of performance was obtained, with IQE of 10.6 %.

Molecular Engineering to Achieve AIE-active Fluorophore with Near-infrared (NIR) Emission and Temperature-sensitive Property.

Near-infrared organic small molecule luminescent materials have the advantages of easy modification, high quantum efficiency, good biological affinity, and color adjustability; thus, have promising application prospects in the fields of photoelectric devices, sensitive detection, photodynamic therapy, and biomedical imaging. However, traditional organic luminescent molecules have the problems of short emission wavelength, aggregation-causing emission quenching, and low quantum yield. Herein, we successfully synthesized four D-π-A-D light-emitting molecules based on electron-withdrawing malonitrile group and different electron-donating arylamine groups. These compounds showed satisfactory solvatochromism, aggregation-induced emission, red and near-infrared fluorescence, high photoluminescence quantum efficiency and temperature response properties. This successful example of molecular engineering provides a valuable reference for the development of advanced NIR materials with AIE and temperature-sensitive properties.

High-Brightness Blue Polariton Organic Light-Emitting Diodes.

Polariton organic light-emitting diodes (POLEDs) use strong light-matter coupling as an additional degree of freedom to tailor device characteristics, thus making them ideal candidates for many applications, such as room temperature laser diodes and high-color purity displays. However, achieving efficient formation of and emission from exciton-polaritons in an electrically driven device remains challenging due to the need for strong absorption, which often induces significant nonradiative recombination. Here, we investigate a novel POLED architecture to achieve polariton formation and high-brightness light emission. We utilize the blue-fluorescent emitter material 4,4'-Bis(4-(9H-carbazol-9-yl)styryl)biphenyl (BSBCz), which exhibits strong absorption and a highly horizontal transition-dipole orientation as well as a high photoluminescence quantum efficiency, even at high doping concentrations. We achieve a peak luminance of over 20,000 cd/m2 and external quantum efficiencies of more than 2%. To the best of our knowledge, these values represent the highest reported so far for electrically driven polariton emission from an organic semiconductor emitting in the blue region of the spectrum. Our work therefore paves the way for a new generation of efficient and powerful optoelectronic devices based on POLEDs.

Efficient tunable white emission and multiple reversible photoluminescence switching in organic Tin(IV) chlorides via regulating the host lattice environment of antimony ions for multifunctional applications

The host lattice environments of Sb3+ has a great influence on its photophysical properties. Here, we synthesized three zero-dimensional organic metal halides of (TPA)2SbCl5 (1), Sb3+-doped (TPA)SnCl5(H2O)·2H2O (Sb3+-2), and Sb3+-doped (TPA)2SnCl6 (Sb3+-3). Compared with the intense orange emission of 1, Sb3+-3 has smaller lattice distortion, thus effectively suppressing the exciton transformation from singlet to triplet self-trapped exciton (STE) states, which makes Sb3+-3 has stronger singlet STE emission and further bring a white emission with a photoluminescence quantum efficiency (PLQE) of 93.4%. Conversely, the non-emission can be observed in Sb3+-2 even though it has a similar [SbCl5]2- structure to 1, which should be due to its indirect bandgap characteristics and the effective non-radiative relaxation caused by H2O in the lattice. Interestingly, the non-emission of Sb3+-2 can convert into the bright emission of Sb3+-3 under TPACl DMF solution treatment. Meanwhile, the white emission under 315 nm excitation of Sb3+-3 can change into orange emission upon 365 nm irradiation, and the luminescence can be further quenched by the treatment of HCl. Therefore, a triple-mode reversible luminescence switch of off-onI-onII-off can be achieved. Finally, we demonstrated the applications of Sb3+-doped compounds in single-component white light illumination, latent fingerprint detection, fluorescent anti-counterfeiting, and information encryption.

Performance-improved narrowband near-ultraviolet emission from a simple butyl and cyanogen substituted indolocarbazole

High-efficiency narrowband near-ultraviolet (NUV) organic light-emitting diodes with high color purity have currently encountered great challenges. Here, using butyl (Bu) and cyanogen (CN) substituted strategy in the simplest polycyclic aromatic hydrocarbons of indolocarbazole (ICz), two simple emitters of BuICz and BuICzCN were demonstrated. This simple strategy was observed to enable both emitters to realize NUV emission at 380–381 nm with a small full width at half maximum (FWHM) of 21–23 nm and high photoluminescent quantum efficiency of 50%–59% in toluene solution. Furthermore, the BuICzCN doped devices exhibited a slightly blueshifted narrowband NUV electroluminescence at 388 nm with a small FWHM of 32.3 nm but a higher external quantum efficiency of 3.92% in comparison with the BuICz doped devices. This work provides a path to realize high-performance narrow-band NUV emission.

Ratiometric thermometry using down-conversion luminescence and solid-state lighting application of Er3+ activated strontium tungstate phosphor

Er3+ activated Sr3WO6 double perovskite crystallized in triclinic structure was synthesized via the solid-state reaction method at 1200 °C for non-contact optical thermometry and solid-state lighting. The phosphors under study were characterized via X-ray diffraction, scanning electron microscopy, diffusion reflectance spectra, and photoluminescence techniques. When excited with 380 nm, the Sr3WO6:Er3+ phosphors exhibited intense green emission, corresponds to 2H11/2/4S3/2-4I15/2 transitions of Er3+. The fluorescence intensity ratio of thermally coupled energy levels were computed within 303–513 K and subsequent relative sensitivity (0.56% K−1 at 303 K) was determined. Moreover, the PL intensity maintained 76.28% at LED burning temperature (150 °C) compared to PL intensity observed at room-temperature, denotes good thermal stability. Additionally, the fluorescent behaviour of the phosphors was examined via PL decay lifetime study. The PL quantum efficiency of the phosphor is computed via the Auzel's model using PL decay lifetime, and was obtained to be 80.32% for Sr3WO6:2% Er3+ phosphor.

Biisoindolylidene solvatochromic fluorophores: Synthesis and photophysical properties

Environment-sensitive fluorescent probes are commonly utilized in various fields, including fluorescence sensing and imaging. This paper describes the synthesis and photophysical properties of a novel class of solvatochromic fluorophores that incorporate biisoindolylidene as the core backbone. This study investigates the structure-property relationships of these newly developed fluorophores. The central biisoindolylidene acts as an efficient electron acceptor, and by modifying the aryl ring substituent at the 3,3′ position, the photophysical properties of the fluorophores can be significantly enhanced, particularly in terms of photoluminescence quantum efficiency. Furthermore, when an electron-donor group replaces the aryl ring at the 3,3′ position, intriguing solvatochromic behavior is observed. This leads to a red-shift in the maximum emission wavelength and an increase in the Stokes shift with increasing solvent polarity. In solvent dimethyl sulfoxide (DMSO), the maximum emission wavelength can reach up to 750 nm, with a Stokes shift of approximately 150 nm. Finally, the potential application of the fluorophore in the detection of volatile acids is explored in a preliminary manner.

Star-shaped hosts based on phenyls substituted carbazole: Effects of trifluoromethyl and tert-butyl moieties

To investigate the effects of trifluoromethyl and tert-butyl moieties on the general optoelectronic properties of star-shaped hosts based on phenyls substituted carbazole, we used 3,6,9-tris (4-(tert-butyl)-phenyl)-9H-carbazole (M1) as a reference, and different numbers of electron-withdrawing 3,5-bis(trifluoromethyl) benzene were introduced into 3, 6 and 9 positions of carbazole to obtain compounds 9-(3,5-bis(trifluoromethyl)phenyl)-3,6-bis(4-(tert-butyl)phenyl)-9H-carbazole (M3), 3,6-bis(3,5-bis(trifluoromethyl)phenyl)-9-(4-(tert-butyl)phenyl)-9H-carbazole (M5) and 3,6,9-tris(3,5-bis(trifluoromethyl)phenyl)-9H-carbazole (M6). After the introduction of 3,5-bis (trifluoromethyl) benzene, the thermal temperature at 5 % mass loss of M3, M5 and M6 decreased to 344 °C, while the glass transition temperature and melting point of M3 and M5 showed a significant increase. However, M6 did not show obvious glass transition, but its melting point also showed a significant increase. M3 crystallized at 125 °C as evidenced by differential scanning calorimetry, and the linking model of M3 is helpful to crystalize. In addition, when compared with those of M1, the fluorescence emission peaks of M3 and M6 showed a blue-shift, while M5 showed a red-shift, all of which were in the deep blue emission range. The color purity of blue light for M1 in tetrahydrofuran solution is the highest, and M1 exhibit aggregation-induced emission characteristics. Compared to the photoluminescence quantum efficiency (PLQY) of compound M1 of 39 % in toluene, the PLQYs of M3 and M6 decreased to 34 % and 29 %, and the PLQY of M5 increased to 46 %. The function of the lowest unoccupied molecular orbital trap of M3 film under the external electrical field will increase, which not only offsets the increasing effect of the electrical field to the electron carrier and further decreases the carrier mobility when the electrical field increase, and the same situation is also feasible for the highest occupied molecular orbital traps in M5, M6 and M1. The organic blue light emitting diodes were prepared by using M1, M3, M5 and M6 as the hosts of bis [2-(4,6-difluorophenyl)pyridinato-C2,N](picolinato)iridium, and the optimized device of M1 as the host showed the best performance with a maximum luminescence brightness of 2978 cd/m2, maximum current efficiency of 39.42 cd/A and maximum external quantum efficiency of 18.36 %.

Tuning the luminescence color of Eu3+- and alkali-ion-codoped Sr2CaWO6 orange-red phosphors: Eu3+ site distribution and site-selective photoluminescence studies

In this study, Eu3+- and alkali-ion (M+)-codoped Sr2CaWO6:x (Eu3+, M+) (x = 0.01–0.10) were synthesized via a solid-state reaction. The effects of different Sr/Ca ratios, types of monovalent metal ions (M+ = Na+, K+, and Li+), and doping concentrations were systematically investigated. The crystalline phase, photoluminescence (PL) properties, lattice site occupied by the Eu3+ ion, Eu3+ site distribution, and site-selective PL properties were evaluated by x-ray diffraction, PL/photoluminescence excitation (PLE) spectroscopy with a monochromatic light source, PL quantum efficiency (QE) measurements, and high-resolution PL/PLE spectroscopy with a wavelength-tunable laser. A dependence of the PL asymmetry ratio for the 5D0–7F1,2 transitions on the Sr/Ca ratio was identified and quantified for the first time. Based on the site-selective PL measurements, this behavior was ascribed to the enhancement of Eu3+ local distortion by Sr2+ substitution at the A site at lower Sr/Ca ratios (<2) and to the high symmetry of the ligand structure of EuO6 octahedra owing to Ca2+ substitution at the B site at higher Sr/Ca ratios (>2). The PLE results provided insight into the Eu3+ site distribution, which explained the orange-red PL and PL QEs of the synthesized phosphors.

Enhancing Light Out-coupling in Perovskite Light-Emitting Diodes through Plasmonic Nanostructures.

Perovskite light-emitting diodes (PeLEDs) have emerged as promising candidates for lighting and display technologies owing to their high photoluminescence quantum efficiency and high carrier mobility. However, the performance of planar PeLEDs is limited by the out-coupling efficiency, predominantly governed by photonic losses at device interfaces. Most notably, the plasmonic loss at the metal electrode interfaces can account for up to 60% of the total loss. Here, we investigate the use of plasmonic nanostructures to improve the light out-coupling in PeLEDs. By integrating these nanostructures with PeLEDs, we have demonstrated an effectively reduced plasmonic loss and enhanced light out-coupling. As a result, the nanostructured PeLEDs exhibit an average 1.5-fold increase in external quantum efficiency and an ∼20-fold improvement in device lifetime. This finding offers a generic approach for enhancing light out-coupling, promising great potential to go beyond existing performance limitations.

Ultrastable Photodetectors Based on Blue CsPbBr3 Perovskite Nanoplatelets via a Surface Engineering Strategy.

Recently, photodetectors based on perovskite nanoplatelets (NPLs) have attracted considerable attention in the visible spectral region owing to their large absorption cross-section, high exciton binding energy, excellent charge transfer properties, and appropriate flexibility. However, their stability and performance are still challenging for perovskite NPL photodetectors. Here, a surface engineering strategy to enhance the optical stability of blue-light CsPbBr3 NPLs by acetylenedicarboxylic acid (ATDA) treatment has been developed. ATDA has strong binding capacity and a short chain length, which can effectively passivate defects and significantly improve the photoluminescence quantum efficiency, stability, and carrier mobility of NPLs. As a result, ATDA-treated CsPbBr3 NPLs exhibit improved optical properties in both solutions and films. The NPL solution maintains high PL performance even after being heated at 80 °C for 2 h, and the NPL film remains nondegradable after 4 h of exposure to ultraviolet irradiation. Especially, photodetectors based on the treated CsPbBr3 NPL films demonstrate exceptional performance, especially when the detectivity approaches up to 9.36 × 1012 Jones, which can be comparable to the best CsPbBr3 NPL photodetectors ever reported. More importantly, the assembled devices demonstrated high stability (stored in an air environment for more than 30 days), significantly exceeding that of untreated NPLs.

Planar Chiral Thermally Activated Delayed Fluorescence Materials Based on Di[2.2]paracyclophane for Circularly Polarized Electroluminescence

AbstractIn this study, featuring di[2.2]paracyclophane (DpCp) amine derivatives as electron donors and 4‐(4,6‐diphenyl‐1,3,5‐triazin‐2‐yl)phenyl (Trz) as the electron acceptor, four thermally activated delayed fluorescence (TADF) molecules are disclosed. The C2 symmetric molecules, DpCpN‐Trz and DpCpCz‐Trz, bearing a chair‐like planar chiral di[2.2]paracyclophane moiety, are obtained as optically pure enantiomers (R/S)‐C‐DpCpN‐Trz and (R/S)‐C‐DpCpCz‐Trz. And the compounds B‐DpCpN‐Trz and B‐DpCpCz‐Trz with a bridge‐like di[2.2]paracyclophane skeleton are meso‐compounds, thus without optically activity. All emitters show blue emissions peaking from 464 to 485 nm, accompanied by high photoluminescence quantum efficiency (up to 93%). The enantiomers (R/S)‐C‐DpCpN‐Trz and (R/S)‐C‐DpCpCz‐Trz exhibit symmetric circularly polarized photoluminescence spectra with dissymmetry factors (|gPL|) ranging from 3.8 × 10−4 to 6.7 × 10−4 in toluene and films. The organic light‐emitting diodes (OLEDs) fabricated with these emitters achieve maximum external quantum efficiencies of up to 19.5%. Notably, the circularly polarized OLEDs (CP‐OLEDs) with (R/S)‐C‐DpCpN‐Trz and (R/S)‐C‐DpCpCz‐Trz demonstrate |gEL| factors of up to 7.6 × 10−4. This study demonstrates a feasible way to design TADF materials and enantiomers by incorporating DpCp derivatives for CP‐OLEDs.

Nondestructive Direct Optical Patterning of Perovskite Nanocrystals with Carbene-Based Ligand Cross-Linkers.

Microscale patterning of colloidal perovskite nanocrystals (NCs) is essential for their integration in advanced device platforms, such as high-definition displays. However, perovskite NCs usually show degraded optical and/or electrical properties after patterning with existing approaches, posing a critical challenge for their optoelectronic applications. Here we achieve nondestructive, direct optical patterning of perovskite NCs with rationally designed carbene-based cross-linkers and demonstrate their applications in high-performance light-emitting diodes. We reveal that both the photochemical properties and the electronic structures of cross-linkers need to be carefully tailored to the material properties of perovskite NCs. This method produces high-resolution (∼4000 ppi) NC patterns with preserved photoluminescent quantum efficiencies and charge transport properties. Prototype light-emitting diodes with patterned/cross-linked NC layers show a maximum luminance of over 60000 cd m-2 and a peak external quantum efficiency of 16%, among the highest for patterned perovskite electroluminescent devices. Such a material-adapted patterning method enabled by designs from a photochemistry perspective could foster the applications of perovskite NCs in system-level electronic and optoelectronic devices.

Single-Component Photochemical Afterglow Near-Infrared Luminescent Nano-Photosensitizers: Bioimaging and Photodynamic Therapy.

Long afterglow luminescence-guided photodynamic therapy (PDT) performs advantages of noninvasiveness, spatiotemporal controllability, and higher signal to noise ratio. Photochemical afterglow (PCA) system emitting afterglow in an aqueous environment is highly suitable for biomedical applications, but still faces the challenges of poor tissue penetration depth and responsive sensitivity. In this work, two novel compounds, Iso-TPA and ABEI-TPA, are designed and synthesized to integrate the PCA system as a single component by coupling near-infrared(NIR) photosensitizers with singlet oxygen cache units, respectively. Both compounds emit NIR afterglow based on photochemical reaction. ABEI-TPA exhibits higher photoluminescence quantum efficiency with nonconjugated linkage, while Iso-TPA with conjugated linkage possesses better reactive oxygen species generation efficiency to achieve stronger PCA and effective PDT, which is ascribed to stronger intramolecular charge transfer effect of Iso-TPA. Iso-TPA nanoparticles can achieve effective long-lasting NIR afterglow in vivo bioimaging up to 120 s with higher imaging resolution and outstanding PDT efficacy of tumor, exhibiting promising potential on bioimaging and therapy.

Iodide manipulation using zinc additives for efficient perovskite solar minimodules

Interstitial iodides are the most critical type of defects in perovskite solar cells that limits efficiency and stability. They can be generated during solution, film, and device processing, further accelerating degradation. Herein, we find that introducing a small amount of a zinc salt- zinc trifluoromethane sulfonate (Zn(OOSCF3)2) in the perovskite solution can control the iodide defects in resultant perovskites ink and films. CF3SOO̶ vigorously suppresses molecular iodine formation in the perovskites by reducing it to iodide. At the same time, zinc cations can precipitate excess iodide by forming a Zn-Amine complex so that the iodide interstitials in the resultant perovskite films can be suppressed. The perovskite films using these additives show improved photoluminescence quantum efficiency and reduce deep trap density, despite zinc cations reducing the perovskite grain size and iodide interstitials. The zinc additives facilitate the formation of more uniform perovskite films on large-area substrates (78-108 cm2) in the blade-coating process. Fabricated minimodules show power conversion efficiencies of 19.60% and 19.21% with aperture areas of 84 and 108 cm2, respectively, as certified by National Renewable Energy Laboratory (NREL), the highest efficiency certified for minimodules of these sizes.

Achieving Nearly 100% Photoluminescence Quantum Efficiency in Organic Radical Emitters by Fine‐Tuning the Effective Donor‐Acceptor Distance

AbstractDonor‐acceptor (D–A•) type luminescent organic radicals have received widespread attention as efficient doublet emitters. However, their generally low photoluminescence quantum efficiency (PLQE) and limited photostability restrict their various applications. Since unraveling the relationship between structure and properties of D–A• type luminescent radicals remains a challenge, here, a series of tri(2,4,6‐trichlorophenyl)methyl (TTM) radical derivatives, which differ by the location of their ring fusion sites and nature of their heteroatoms, is synthesized. The PLQE of isomers varies by ten times as a function of ring fusion sites. In particular, the PLQE of a radical undergoing ring fusion at the carbazole 3,4‐position is as high as 98.0%. Quantum‐chemical calculations show that in the case of overlapping holes and electrons, by increasing the effective distance between the D and A moieties, the radiative transition rates of the radicals increase. Also, decreasing the electronic coupling between the charge‐transfer and local‐excited states and avoiding large geometrical distortions between the ground state (D0)_and the first excited state (D1) can significantly reduce the nonradiative transition rates. This work offers a design strategy to obtain efficient and stable luminescent radicals by modifying the sites of ring fusion, which allows control of the radiative and nonradiative transition rates.

Large‐Scale Room‐Temperature Synthesis of the First Sb3+‐Doped Organic Ge(IV)‐Based Metal Halides with Efficient Yellow Emission for Solid‐State Lighting and Latent Fingerprint Detection

Organic–inorganic hybrid Ge(II)‐based metal halides have garnered significant interest due to their intriguing photophysical properties and environmentally friendly characteristics. However, challenges such as poor stability, low emission intensity, and a complex synthesis process have hindered their widespread application. In addressing these issues, a breakthrough in the large‐scale production of Sb3+‐doped Ge(IV)‐based metal halide (C13H14N3)2GeCl6 phosphors at room temperature through a straightforward solution method is presented. The synthesized compound exhibits a remarkable bright broad yellow emission band at 590 nm, boasting a photoluminescence quantum efficiency of 99.53 ± 0.06% the highest among Ge(IV)‐based metal halides. Notably, the introduction of Sb3+ induces the formation of Jahn–Teller‐like self‐trapped excitons in [SbCl6]3− species, attributable to lattice distortion and strong electron–phonon coupling. Consequently, Sb3+‐doped (C13H14N3)2GeCl6 demonstrates a large Stokes shift (221 nm) and a prolonged decay lifetime (3.06 μs). Furthermore, the Sb3+‐doped compound exhibits commendable chemical‐ and photostability, prompting exploration in applications such as white light‐emitting diodes and latent fingerprint detection. This work not only provides a practical approach for designing economically viable, environmentally friendly, and highly efficient emission phosphors but also paves the way for novel directions in their expanded application.