首页|期刊导航|陶瓷学报|白光LED用Eu3+激活红色荧光粉的激发光谱调控策略与研究进展

白光LED用Eu3+激活红色荧光粉的激发光谱调控策略与研究进展OA

Strategies and Progress in Excitation Spectrum Modulation of Eu3+-activated Red Phosphors for White Light-emitting Diodes

中文摘要英文摘要

白光发光二极管(WLED)作为新一代固态照明光源,其性能高度依赖于荧光粉的光学特性.Eu3+激活的红色荧光粉因其色纯度高、稳定性好等优势备受关注,但其在近紫外区的激发峰为窄线状吸收,导致与商用近紫外 LED 芯片的光谱匹配度差、吸收效率低,严重制约了其在高显色指数 WLED 中的应用.本文系统综述了近年来为解决此关键瓶颈而发展的四种主要策略:(1)通过晶体结构工程提高 Eu3+掺杂浓度以增加吸收位点;(2)引入 Sm3+、Tb3+或 Bi3+等敏化离子,利用高效的能量传递拓宽并增强激发响应;(3)将高性能荧光粉集成为块体转换体(如致密陶瓷、透明陶瓷及荧光粉-玻璃复合体),通过宏观构型调控延长激发光程、提升有效吸收;(4)理性设计基质材料,调控电荷迁移带(CTB)或金属-金属电荷转移(MMCT)过程,以获得位于近紫外区的宽带强吸收.本文详细评述了各策略的研究现状、内在机理、代表性成果及面临的挑战,并对未来高性能 Eu³⁺激活红色荧光粉的设计与开发进行了展望,旨在为推动全光谱、高显色 WLED 技术的发展提供理论参考.

[Significance]White light-emitting diodes(WLEDs)have emerged as the dominant next-generation solid-state lighting technology,valued for their energy efficiency,long lifespan and environmental friendliness.A critical factor determining WLED performance,particularly color rendering index(CRI)and correlated color temperature(CCT),is optical properties of the down-conversion phosphors used in conjunction with LED chips.While blue-pumped YAG:Ce3+-based WLEDs are commercially prevalent,they suffer from a deficiency in red spectral components,resulting in high CCT and low CRI,which limits their suitability for high-quality illumination.An alternative and superior approach employs near-ultraviolet(NUV,380-420 nm)LED chips combined with red,green and blue(RGB)tri-phosphors to achieve full-spectrum high-CRI(>90)white light.However,the development of efficient NUV-excitable red phosphors remains a major bottleneck.Eu³⁺-activated red phosphors are highly attractive,due to their excellent color purity(dominant 5D0→7F2 emission at~615 nm),chemical/thermal stability and low cost.Nevertheless,their practical application is severely hindered by intrinsically weak and narrow-line f-f excitation peaks at about 395 nm,which exhibit poor spectral overlap with commercial NUV LED chips,leading to low absorption efficiency.Overcoming this fundamental limitation is therefore of paramount significance for advancing high-performance full-spectrum WLED technologies. [Progress]To address the weak NUV absorption of Eu3+,researchers have developed four primary strategies,each with distinct mechanisms and varying degrees of success.Firstly,high-concentration doping is used to increase the number of Eu³⁺absorption sites.By engineering crystal structures with large cationic distances or insulating polyhedral networks,non-radiative concentration quenching can be mitigated,enabling doping concentrations up to 100%and significantly enhanced absorption.However,the improvement in absorption efficiency remains modest(typically<40%)and the intrinsic line-like nature of the absorption is unchanged.Secondly,sensitization via co-doping introduces ions like Sm3+,Tb3+or Bi3+,which possess stronger or broader absorption bands.Sm3+and Tb3+can absorb light at specific NUV wavelengths and transfer energy to Eu³⁺,but their own narrow absorption limits the overall gain.In contrast,Bi3+,with its intense,spin-allowed 1S0→3P1 broadband transition in the NUV region,has shown greater promise.Notably,systems like LiKBi2(MoO4)4:Eu3+have achieved an ultrabroad excitation band(200-400 nm)and a high external quantum efficiency(EQE)of 84.7%,primarily through Bi3+→Mo6+metal-metal charge transfer(MMCT).Thirdly,macroscopic structural engineering focuses on enhancing light-matter interaction by fabricating phosphors as dense ceramics,transparent ceramics or phosphor-in-glass(PiG)composites.These architectures extend the effective optical path length of the incident NUV light,thereby increasing the probability of absorption.Transparent ceramics,in particular,offer excellent thermal management and high optical quality,but require complex high-cost fabrication processes.Finally,host matrix engineering seeks to create intrinsic broadband NUV absorption by rationally designing the host to position its charge transfer band(CTB)or MMCT band within the NUV window.Molybdate and tungstate hosts containing[MoO6]octahedra have been extensively explored for this purpose,as their CTB can be tuned into the NUV range,providing a direct and efficient excitation channel for Eu3+. [Conclusions and prospects]In summary,while significant advances have been made in enhancing the NUV excitation of Eu3+-activated red phosphors,no single strategy yet delivers an ideal combination of strong broadband absorption,high quantum efficiency,stability and cost-effective scalability.Future efforts should prioritize synergistic approaches:refining host engineering through predictive crystal-chemical design to tune charge transfer bands into the 380-410 nm range,optimizing Bi3+co-doping by tailoring its local coordination to maximize energy transfer and developing scalable fabrication methods for transparent or glass-integrated phosphor architectures.Achieving these goals will enable the practical deployment of Eu3+-based red phosphors in high-CRI full-spectrum WLEDs for human-centric lighting applications.

王三海;徐彦乔;胡庆;徐志芳;王连军;江莞

景德镇陶瓷大学 材料科学与工程学院,江西 景德镇 333403景德镇陶瓷大学 国家日用及建筑陶瓷工程技术研究中心,江西 景德镇 333403景德镇陶瓷大学 材料科学与工程学院,江西 景德镇 333403中国轻工业陶瓷研究所,江西 景德镇 333001景德镇陶瓷大学 国家日用及建筑陶瓷工程技术研究中心,江西 景德镇 333403||东华大学 材料科学与工程学院,上海 201620景德镇陶瓷大学 国家日用及建筑陶瓷工程技术研究中心,江西 景德镇 333403||东华大学 材料科学与工程学院,上海 201620

化学化工

白光 LEDEu3+红色荧光粉激发峰电荷迁移带能量传递

white LEDEu3+red phosphorexcitation peakcharge transfer bandenergy transfer

《陶瓷学报》 2026 (2)

267-281,15

国家重点研发项目(2021YFB3500504)江西省自然科学基金(20224BAB214024,20232BAB204012,20232BAB204015).

10.13957/j.cnki.tcxb.2026.02.004

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