High Photoluminescence Quantum Yield Research Articles

Ultra-Broad Emission Copper Halide Scintillator-Based X-Ray Imager.

Lead-free metal-halide scintillators are gaining considerable attention as more eco-friendly and superior alternatives to their lead-based counterparts. However, novel broad-emission band scintillators like the state-of-the-art CsI: Tl scintillator, which can generate high signals due to its strong compatibility with the spectral responsivity of regular photodiode arrays, are still less investigated. Herein, a TPA2Cu2I4 (TPACI) copper halide scintillator with a unique ultra-broad emission (FWHM > 240nm) is developed, which shows universal compatibility with the peak response range of commercial photodetector. The optical properties characterization and mechanism analysis indicates that this ultra-broad spectrum can be attributed to the dual self-trapped exciton (STE) emission consisting of two emission bands. Benefiting from the large Stokes shift and ultra-broad emission band enabled by the dual STE, the self-absorption-free TPACI scintillator exhibits efficient white light emission with a high photoluminescence quantum yields of 94.27%, a high light yield of ≈40124 photons MeV-1. Moreover, a prototype of a TPACI scintillator-based X-ray imager is assembled for inspecting the internal structures of biological and electronic devices, which demonstrated a high resolution of 5.5 lp mm-1 at modulation transfer function = 0.2. These findings provide insights into the design of efficient, broad-emission scintillators for high-resolution X-ray imaging.

Rational Molecular Design for Balanced Locally Excited and Charge- Transfer Nature for Two-Photon Absorption Phenomenon and Highly Efficient TADF-Based OLEDs.

The pursuit of highly efficient thermally activated delayed fluorescence (TADF) emitters with two-photon absorption (2PA) character is hampered by the concurrent achievement of a small singlet-triplet energy gap (ΔEST) and high photoluminescence quantum yield (ФPL). Here, by introducing a terephthalonitrile unit into a sterically crowded donor-π-donor structure, inducing a hybrid electronic excitation character, we designed unique TADF emitters possessing 2PA ability. This rational molecular design was achieved through a main π-conjugated donor-acceptor-donor backbone in line with locally excited feature renders a large oscillator strength and transition dipole moment, maintaining a high 2PA cross-section value. The ancillary N-donor-acceptor-donor with charge transfer character highly balances the TADF phenomenon by minimizing ΔEST. A near-unity ФPL value with a large radiative decay rate over an order of magnitude higher than the intersystem crossing rate and a high horizontal orientation ratio of 0.95 were simultaneously attained for TPCz2NP. The organic light-emitting diodes fabricated with this material exhibit a high maximum external quantum efficiency of 25.4% with an elevated 2PA cross-section (σ2) value up to 143GM at 850 nm. These findings offer a venue for designing high-performance TADF emitters with exceptional performance inclusive of 2PA properties, expanding for future functional material design.

Rational Molecular Design for Balanced Locally Excited and Charge‐ Transfer Nature for Two‐Photon Absorption Phenomenon and Highly Efficient TADF‐Based OLEDs

The pursuit of highly efficient thermally activated delayed fluorescence (TADF) emitters with two‐photon absorption (2PA) character is hampered by the concurrent achievement of a small singlet‐triplet energy gap (ΔEST) and high photoluminescence quantum yield (ФPL). Here, by introducing a terephthalonitrile unit into a sterically crowded donor‐π‐donor structure, inducing a hybrid electronic excitation character, we designed unique TADF emitters possessing 2PA ability. This rational molecular design was achieved through a main π‐conjugated donor‐acceptor‐donor backbone in line with locally excited feature renders a large oscillator strength and transition dipole moment, maintaining a high 2PA cross‐section value. The ancillary N‐donor‐acceptor‐donor with charge transfer character highly balances the TADF phenomenon by minimizing ΔEST. A near‐unity ФPL value with a large radiative decay rate over an order of magnitude higher than the intersystem crossing rate and a high horizontal orientation ratio of 0.95 were simultaneously attained for TPCz2NP. The organic light‐emitting diodes fabricated with this material exhibit a high maximum external quantum efficiency of 25.4% with an elevated 2PA cross‐section (σ2) value up to 143 GM at 850 nm. These findings offer a venue for designing high‐performance TADF emitters with exceptional performance inclusive of 2PA properties, expanding for future functional material design.

Copper-Iodide Hybrid Clusters with Partial Distortion Enable High-Performance Full-Visible-Spectrum White-Light-Emitting Diodes.

Phosphor-converted white-light-emitting diodes (pc-WLEDs) have become increasingly prevalent artificial light sources. Currently, multicomponent phosphors are commonly used for pc-WLEDs, but they often suffer from issues of undesirable reabsorption and unstable emission colors. The potential alternative for pc-WLEDs is a single-component white phosphor that covers the broad visible spectrum with desirable low thermal quenching and efficient luminescence, which is still scarce. To address this challenge, we design a unique single-component white phosphor based on Cu4I4(4-(tert-butyl)-2-(diphenylphosphaneyl)pyridine)2 (Cu4I4(NP-tBu)2) hybrid clusters, which exhibits ultrabroad dual emission from 400 to 800 nm and a high photoluminescence quantum yield of 97% under 320 nm light excitation. Based on time-resolved fluorescence spectroscopy and theoretical model analysis of our Cu4I4 series clusters, we hypothesize that the dual emission comes from the coexistence of two triplet states caused by partial cluster distortion under light excitation. The Cu4I4(NP-tBu)2 cluster's high structural stability also endows consistent spectral performance and low thermal quenching up to 240 °C. Thus, the fabricated pc-WLED using Cu4I4(NP-tBu)2 white phosphor exhibits a maximum efficiency of 63.4 lm/W and maintains a high color rendering index of ∼88 during 1000 h of continuous operation. Our results highlight a new strategy of low-cost and high-performance copper-iodide cluster-based single-component white phosphors for high-quality pc-WLEDs.

Surface Electric Dipole Moment Engineering of All‐Inorganic Transparent Solid Matrix for Information Encryption and X‐Ray Imaging

AbstractPerovskite nanocrystals (PNCs) show excellent optoelectronic performance and controlled synthesis of PNCs is arising as research hot spot recently. Transparent all‐inorganic glass matrix has been proved perfect protector of PNCs from aggregation. However, the precise precipitation of PNCs in glass with high photoluminescence quantum yield (PLQY) through a facile routing is still challenge. Here, site‐specifically crystallization of PNCs are rationally designed in all‐inorganic transparent solid matrix through surface electric dipole moment engineering, achieving exceptional PLQY (89.9%). Modifying the orientation of the surface electric dipole moment reduces the water‐induced nucleation barrier and promotes the crystallization of PNCs at the selected sites. In addition, the inherent ionic structure and low formation energy of CsPbBr3 PNCs allow the luminescent structure to be erased by annealing and then recovered by water‐inducing. Combining the intense luminescence, high stability and completely reversable crystallization, the applications of PNCs‐glass in information encryption and reusable X‐ray dosimeter and imaging are demonstrated. The PNCs‐glass scintillation screen achieves the X‐ray imaging resolution of 17.5 lp mm−1, which is the highest among all the PNCs based scintillation screen.

Multifunctional Molecule Passivated Quasi‐2D Perovskite Film for Efficient and Stable Luminescent Solar Concentrator

AbstractQuasi−2D perovskite films with multiple quantum well structures can provide a large Stokes shift and efficient photoluminescence (PL), which have great potential in the application of luminescent solar concentrators (LSCs). However, its low photoelectric conversion efficiency and poor stability remain obstacles to commercial application. Here, a multifunctional molecule additive octyltriphenylphosphonium bromide is introduced to prepare high‐quality perovskite LSCs. The multifunctional molecule can simultaneously passivate perovskite cations and anions, reducing the defect sites and improving the photoluminescence quantum yield (PLQY) of the perovskite nanocrystals. Triphenylphosphine groups with high steric hindrance effect can hinder ion migration; the hydrophobic properties of the long alkyl chain prevent water erosion, which together improves the stability of the perovskite films. The multifunctional molecule passivated perovskite film has a high PLQY of 100% and retains 96% of the initial PL intensity after 30 days of indoor storage. The perovskite LSC device achieves a maximum optical efficiency of 6.5% at a geometric factor of 3.1. The findings open a new way to boost the performance of perovskite‐based LSCs.

Hybrid-Protected Perovskite Quantum Dot Films with Ultra-High Efficiency and Stability for LED Backlighting.

All-inorganic lead halide perovskite quantum dots (PQDs) have emerged as highly promising materials for photonic and optoelectronic devices, solar cells, and photocatalysts. However, PQDs encounter instability and color separation issues because of ion diffusion. Current strategies mainly address stability in green CsPbBr3 PQDs, with limited focus on the red-mixed halide PQDs because of their inferior stability compared with green PQDs. Our study provides a new dual-protection methodology for synthesizing high-efficiency green and red mixed-halide PQD films. Red CsPb(Br0.4I0.6)3 and green CsPbBr3 PQDs are embedded with silicone resin and then incorporated with poly(methyl methacrylate) (PMMA) matrix to form red and green PQDs@silicone/PMMA films. The high photoluminescence quantum yield (PLQY) and great stability are recorded for the pure-red PQD polymer film. The ultrabright green CsPbBr3 PQDs@silicone/PMMA film was also successfully fabricated with an outstanding PLQY beyond 94%. These films exhibited enhanced stability against thermal and environmental degradation, attributed to the dense protective layer of silicone resin and PMMA matrices by the formation of Si-halide and Pb-O bonds, thereby reducing surface defects. Theoretical calculations reveal that combining silicone resin and PMMA improves Pb-O interactions, eliminating uncoordinated Pb2+ and enhancing PQD stability. Applied to white light-emitting diodes (WLEDs), these films demonstrated a broad color gamut of 143.4%, indicating their potential for efficient WLED backlighting.

Reducing Non-Radiative Energy Losses in Non-Fullerene Organic Solar Cells.

With the rapid advancement of non-fullerene acceptors (NFAs), the power conversion efficiency (PCE) of organic solar cells (OSCs) has surpassed the 20 % threshold, highlighting their considerable potential as next-generation energy conversion devices. In comparison to inorganic or perovskite solar cells, the open-circuit voltage (Voc) of OSCs is constrained by substantial non-radiative energy losses (ΔEnr), leading to values notably below those anticipated by the Shockley-Queisser limit. In OSCs, non-radiative energy losses are intimately associated with the electroluminescent quantum efficiency (EQEEL) of charge transfer states, which is in turn directly affected by the photoluminescence quantum yield (PLQY) of acceptor materials. Consequently, enhancing the PLQY of low-bandgap acceptor materials has emerged as a pivotal strategy to effectively mitigate ΔEnr. This review article delves into the intrinsic correlation between molecular structure and PLQY from the vantage point of acceptor material design. It further explores methodologies for designing acceptor materials exhibiting high PLQY, with the ultimate goal of realizing OSCs that combine high efficiency with minimal ΔEnr.

TADF‐Emitting Nanoparticles for Application as Probes in Time‐Resolved Imaging and 1O2 Photosensitizers

AbstractOrganic Thermally Activated Delayed Fluorescence (TADF) molecules are luminescent compounds capable of harvesting energy from triplet states without using heavy metals. This process results in oxygen‐sensitive, long‐lived delayed emission, suitable for developing optical probes for time‐gated cell imaging, oxygen sensors, and singlet oxygen photosensitizers. Despite their potential, the use of TADF emitters in these applications is hindered by poor performance in polar media and the challenge of balancing high photoluminescence quantum yields, long emission lifetimes, and high triplet formation quantum yields. In this study, novel TADF emitters are developed based on 1,8‐naphthalimide (NI) dyes, and how encapsulation in polymeric nanoparticles can enhance their performance in aqueous media is demonstrated. The resulting nanomaterials exhibit high delayed‐to‐prompt emission ratios, long delayed fluorescence lifetimes, and exceptional applicability in time‐resolved imaging. The singlet oxygen photosensitization capabilities of the TADF nanomaterials in the photodegradation of phenol, exploring a Förster Resonance Energy Transfer (FRET) system that improved the efficiency, are also assessed. These findings highlight the promising potential of TADF nanomaterials for diverse applications, including photodegradation of pollutants, cellular imaging, and biosensing.

Highly Efficient Blue Organic Light‐Emitting Devices Based on “Cross”‐Shaped Hot Exciton Emitters

AbstractThe development of blue electroluminescent (EL) materials remains a significant challenge in organic light‐emitting diode (OLED) technology. In this study, a novel design strategy is proposed for blue hot exciton (HE) materials, which involves utilizing a “cross” shaped molecular structure characterized by substantial steric hindrance and a highly twisted conformation. The unique cross‐shaped molecular architecture with distinct “arms” enables flexible control over the excited state properties of the molecule, thereby facilitating precise modulation of high‐lying triplet and low‐lying singlet excited state energy levels. Furthermore, the 3D spatial configuration of the molecule effectively reduces close molecular packing, thereby minimizing the risk of material concentration quenching. The proof‐of‐concept HE emitters CN‐PI and TP‐PI exhibit non‐π‐π stacking configurations in single crystals, achieving high photoluminescence quantum yield (PLQY) values up to 51.3% and 46.5% in non‐doped thin films, respectively, along with rapid radiation decay rates and reasonable distribution of Tm (m ≤ 5) and S1 states. Non‐doped OLEDs incorporating these emitters demonstrate exceptional external quantum efficiencies (EQE), reaching 7.3% and 6.4%, respectively, while exhibiting minimal efficiency roll‐off at high luminance. This research introduces a promising approach for developing high‐performance blue HE emitters.

Precursor Reactivity‐Controlled Synthesis of ZnSeTe Spherical Quantum Wells with Narrow and Symmetric Photoluminescence

AbstractEnvironment‐friendly ZnSeTe quantum dots (QDs) are considered as potential blue light emitters. However, due to the large reaction activity difference between Se and Te precursors, ZnSeTe QDs usually can not uniformly alloyed and generate lattice distortion, reducing the color purity or photoluminescence quantum yield (PLQY). A ZnSe/ZnSeTe/ZnSe spherical quantum well (SQW) structure with quasi type‐II energy band arrangement is designed. To promote the uniform growth and even alloying of ternary ZnSeTe, weakly active biphenyltellurium (Ph2Te2) is applied as a new Te source for balancing the reactivity between Te and Se. Epitaxial growth of high crystallinity ZnSeTe with greatly reduced defects is obtained. After ZnS outer layer passivation, the obtained ZnSe/ZnSeTe/ZnSe/ZnS QDs exhibit a high PLQY (≈84%) and a narrow full width at half maxima (19 nm) without asymmetric broaden at 455 nm, contributing to an ultrahigh color purity, which is among the best photoluminescence performance for blue emitting ZnSeTe based QDs. This work provides a new balance strategy of precursor reactivity for synthesizing high color purity and heavy metal free blue ZnSeTe QDs.

Cu‐Catalyzed Oxidative Tandem Coupling and Cyclization of 2‐Aminonaphthalenes to Synthesize Dibenzo[c, g]carbazoles

AbstractA Cu(II) complex with a bipyridyl ligand bearing a Brønsted acid was used to catalyze the tandem oxidative coupling and cyclization of 2‐aminonaphthalenes to give N‐substituted‐dibenzo[c,g]carbazoles. The incorporation of an appended acidic moiety to the ligand was found to be key to the selective formation of dibenzocarbazoles over 2,2’‐diamino‐1,1’‐binaphthalene (BINAM), which is known as an irreversible byproduct. This highly efficient method yields a wide array of dibenzo[c,g]carbazoles featuring diverse functional groups as well as electronic properties. The selected dibenzo[c,g]carbazoles exhibited high photoluminescence quantum yields of up to 100 % and are promising chromophores for advanced materials.

Thickness and Doping Density Influence of a High-Voltage Inorganic Perovskite Solar Cell: A SCAPS 1-D Simulation Study

Recently, all inorganic perovskite solar cells have triggered great attention thanks to the rising performance during their development in solid state photovoltaics showing enhanced characteristics, such as: good stability, high photoluminescence quantum yield, tunable size, and morphology. In this work, a high open-circuit voltage solar cell based on all-inorganic perovskite through SCAPS simulator program is presented by analysing electron transport layer (ETL), perovskite layer, hole transport layer (HTL) thickness and doping density from a FTO/TiO2/CsPbBr3/Spiro-OMeTAD/Au structure were modified to observe its influence on solar cell performance. Therefore, simulation results show that a thicker ETL hinders carrier transport towards the FTO layer due to larger distance which leads to higher recombination rate, reducing carrier’s lifetime. Albeit high doping density values in ETL enhances the overall solar cell performance. As for the absorber layer, while its thickness increases, carrier collection rate decreases due to recombination impacting Voc, which results from thickness increase. Based on the results, solar cell efficiency improvement is attributed to the built-in electric field as absorber layer doping density increases. While HTL thickness has minimum impact on the solar cell output, doping density enhances device parameters significantly. Summarising the results obtained from thickness and doping density simulations, the optimal solar cell operation was obtained at 10 nm, 600 nm, and 100 nm layer thickness as well as 1020 cm-3, 1016 cm-3, and 1020 cm-3 doping density (TiO2, CsPbBr3 and Spiro-OMeTAD). Results from three different sources, collected from literature, were used to compare, and fitting them along with simulation results.

Oriented Growth of Highly Emissive Manganese Halide Microrods for Dual‐Mode Low‐Loss Optical Waveguides

AbstractZero‐dimensional (0D) structured lead‐free metal halides have recently attracted widespread attention due to their high photoluminescence quantum yield (PLQY) and negligible self‐absorption, showing enormous potential as optical waveguides towards miniaturized photonic devices. However, due to the great difficulty in growth of rod‐like nano/micro‐sized morphologies, such applications have been less explored. Herein, a new‐type emissive organic–inorganic manganese (II) halide crystal (TPS2MnCl4, TPS=C18H15S, triphenylsulfonium) in the form of microrods is synthesized via a facile chloride ion (Cl−) induced oriented growth method. Due to a combination of attractive features such as a high PLQY of 86 %, negligible self‐absorption and smooth crystal surface, TPS2MnCl4 microrods are well suited for use in optical waveguide with an ultra‐low optical loss coefficient of 1.20 ⋅ 10−4 dB μm−1, superior to that of most organic–inorganic metal halide hybrids, organic materials, polymers and metal nanoclusters to the best of our knowledge. Importantly, TPS2MnCl4 microrods can further work as dual‐mode optical waveguides, combining active and passive light transmission functionalities in one single crystal. In addition, TPS2MnCl4 microrods also display remarkable performance in lighting and anti‐counterfeiting due to their distinct optical properties and commendable stability.

Oriented Growth of Highly Emissive Manganese Halide Microrods for Dual-Mode Low-Loss Optical Waveguides.

Zero-dimensional (0D) structured lead-free metal halides have recently attracted widespread attention due to their high photoluminescence quantum yield (PLQY) and negligible self-absorption, showing enormous potential as optical waveguides towards miniaturized photonic devices. However, due to the great difficulty in growth of rod-like nano/micro-sized morphologies, such applications have been less explored. Herein, a new-type emissive organic-inorganic manganese (II) halide crystal (TPS2MnCl4, TPS=C18H15S, triphenylsulfonium) in the form of microrods is synthesized via a facile chloride ion (Cl-) induced oriented growth method. Due to a combination of attractive features such as a high PLQY of 86 %, negligible self-absorption and smooth crystal surface, TPS2MnCl4 microrods are well suited for use in optical waveguide with an ultra-low optical loss coefficient of 1.20 ⋅ 10-4 dB μm-1, superior to that of most organic-inorganic metal halide hybrids, organic materials, polymers and metal nanoclusters to the best of our knowledge. Importantly, TPS2MnCl4 microrods can further work as dual-mode optical waveguides, combining active and passive light transmission functionalities in one single crystal. In addition, TPS2MnCl4 microrods also display remarkable performance in lighting and anti-counterfeiting due to their distinct optical properties and commendable stability.

Progress on perovskite quantum dots and light-emitting diodes

Abstract. Perovskite quantum dots have become a popular material for the development of new high-efficiency light-emitting diodes (LED) because of their high photoluminescence quantum yield, adjustable luminescence spectrum, narrow spectral width, high defect tolerance and unique quantum limit effect. We review the recent progress based on LED of different types of perovskite quantum dots. First, the properties, existing problems and applications of fully inorganic perovskite quantum dots are introduced. Subsequently, both organic and inorganic perovskites and their applications are discussed, and several methods to improve the LED efficiency of perovskite quantum dots are explored. Finally, this paper analyzes the current challenges of LED of perovskite quantum dots, such as instability and toxicity, and its application prospect in the field of high-efficiency display and lighting is discussed. That is, the EQE of LED based on perovskite quantum dots has increased to more than 20% in four years, and the service life has been extended to tens of hours. This review provides useful insights for the development of more efficient and safer perovskite quantum dot luminescence devices.

Simple synthesis of AgInS2/ZnS core/shell quantum dots with wide tunable emission wavelength for white light-emitting diodes

Phosphor with efficient and broad range emission is necessary for lighting applications. I-III-VI group quantum dots (QDs) have the advantages of non-toxic composition and large adjustable spectrum range, and have potential applications in the field of lighting. However, the efficient luminescence of these QDs at shorter wavelengths still needs further study, which is crucial for the development of high color rendering index white light LED devices (WLEDs). In this work, wide visible range emitting AgInS2/ZnS QDs with broad band and high luminous efficiency were obtained by altering the Ag/In ratios and Zn2+ inter-diffusion with cation of AgInS2. Photo-luminescent (PL) wavelength range of the obtained core-shell structured AgInS2/ZnS extended from 703 nm to 524 nm with high PL quantum yield (QY) and stability. The champion device based on the optimized AgInS2/ZnS QDs exhibits warm white light (correlated color temperature = 3652 K) characteristics with high color rendering index (CRI Ra) of 92.85 while maintaining excellent color stability under different driving currents. These properties are far superior to those of WLEDs with YAG phosphor.

Simple‐Structure and Anti‐Quenching Deep‐Blue Multi‐Resonance TADF Emitters Enable High‐Efficiency OLEDs with BT.2020 Blue Gamut

AbstractDeveloping highly efficient pure‐blue organic light‐emitting diodes (OLEDs) that meet the stringent BT.2020 standard by using multi‐resonance thermally activated delayed fluorescence (MR‐TADF) materials has long been a formidable challenge. In this study, a strategy is demonstrated for high‐performance blue MR‐TADF emitters by gradually decorating the MR framework with alkyl groups, and subsequently introducing a diarylamino group at the para‐position of boron atom. The proof‐of‐concept molecule, IPrBN‐mCP, exhibits a narrowband deep‐blue emission peaking at 452 nm, with a very narrow full‐width at half maximum (FWHM) of 19 nm in solution, and a remarkably high photoluminescence quantum yield (PLQY) approaching unity in doped films. As a result, OLEDs based on IPrBN‐mCP achieve not only a high maximum external quantum efficiency (EQEmax) of 33.4% but also ultrapure blue emission with a Commission Internationale de L'Eclairage (CIE) y value of 0.046, fully satisfying the BT.2020 blue standard. This represents the first OLED example fully meeting the rigorous color requirements of the BT.2020 blue standard while simultaneously achieving an EQE exceeding 30%.

Chiral Rare-Earth (Ce, Eu) Metal Halides with Bright Circularly Polarized Luminescence.

Chiral metal halide materials are emerging chiroptical materials that are easy to synthesize and have a wide tunability. Rare-earth (RE) metals are desirable components to be incorporated in the hybrid regime; however, they are typically difficult to handle for solution-based halide chemistry. Here, we report two new examples of chiral RE metal halides with Ce(III) and Eu(III) with chiral alkanolammonium cations (R/S-3-hydroxyquinuclidium). These compounds crystallize in the non-centrosymmetric space group R3, where their mirror-like symmetric circular dichroism (CD) and circularly polarized luminescence (CPL) further witness the chiral nature. The superior emission properties, including the high photoluminescence quantum yield of the Ce-based materials (84-90%) and Eu-based materials (27-29%), have led to distinct and sharp symmetrical CPL in the ultraviolet and visible regions, with dissymmetry factors (glum) of ∼2 × 10-3 and ∼4 × 10-3, respectively. This work has established and expanded the materials space for chiral RE metal halides and demonstrated their potential for chiroptical and spintronic applications.

Loading Dyes into Chiral Cd/Zn‐Metal–Organic Frameworks for Efficient Full‐Color Circularly Polarized Luminescence

AbstractHost‐guest chemistry of chiral metal‐organic frameworks (MOFs) has endowed them with circularly polarized luminescence (CPL), it is still limited for MOFs to systematically tune full‐color CPL emissions and sizes. This work directionally assembles the chiral ligands, metal sites and organic dyes to prepare a series of crystalline enantiomeric D/L‐Cd/Zn‐n MOFs (n=1~5, representing the adding amount of dyes), where D/L‐Cd/Zn with the formula of Cd2(D/L–Cam)2(TPyPE) and Zn2(D/L–Cam)2(TPyPE) (D/L‐Cam=D/L‐camphoric acid, TPyPE=4,4’,4’’,4’’’‐(1,2‐henediidenetetra‐4,1‐phenylene)tetrakis[pyridine]) were used as the chiral platforms. The framework‐dye‐enabled emission and through‐space chirality transfer facilitate D/L‐Cd/Zn‐n bright full‐color CPL activity. The ideal yellow CPL of D‐Cd‐5 and D‐Zn‐4, with |glum| as 4.9 × 10−3 and 1.3×10−3 and relatively high photoluminescence quantum yield of 40.79 % and 45.40 %, are further assembled into a white CPL light‐emitting diode. The crystal sizes of D/L‐Cd/Zn‐n were found to be strongly correlated to the types and additional amounts of organic dyes, that the positive organic dyes allow for the preparation of > 7 mm bulks and negative dyes account for sub‐20 μm particles. This work opens a new avenue to fabricate full‐color emissive CPL composites and provides a potentially universal method for controlling the size of optical platforms.