Perovskites form an important and enormous class of inorganic compounds. Recently, perovskite materials have attracted extensive research interest owing to their excellent optoelectronic properties. Deep insights into the relationships between the crystal structure, electronic structure and properties play an important role in the development of new functional materials and high-performance devices. In this review, after a brief introduction, we first discuss the crystal structure and crystal chemistry of perovskites according to their three classes: standard perovskites, low-dimensional perovskites and perovskite-like halides. Next, the electronic structure and luminescence from different physical origins are presented. Then, we present a survey on the design, synthesis and luminescence properties of different perovskites, including halide perovskites, oxide perovskites, and lanthanide- or transition metal-doped perovskites, also including dimension-different perovskites (3D, 2D, 1D and quantum dots). We also summarize the strategies for improving the photoluminescence quantum yield (PLQY) and chemical stability, including by surface passivation, encapsulation and doping. Finally, we review their applications and give a brief outlook.

Luminescent perovskites: recent advances in theory and experiments

Ultra-high color rendering warm-white light-emitting diodes based on an efficient green-emitting garnet phosphor for solid-state lighting

A red phosphor LaSc3(BO3)4:Eu3+ with zero-thermal-quenching and high quantum efficiency for LEDs

Luminescence and self-referenced optical temperature sensing performance in Ca2YZr2Al3O12:Bi3+,Eu3+ phosphors

Inorganic phosphors with broadband near-ultraviolet (near-UV) excitation and efficient visible emission are highly important for fabricating high-performance near-UV-pumped white light-emitting diodes (LEDs). Herein, we report on novel efficient near-UV-excitable Ce3+/Tb3+ ion co-activated Ca2YHf2Al3O12 (CYHA) green-emitting garnet phosphors, which were successfully prepared through a high-temperature solid-state reaction process. X-ray diffraction, field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, elemental mapping, photoluminescence, CIE color coordinates, the internal and external quantum efficiency, and temperature-dependent emission spectra were used to characterize the samples. Interestingly, due to the efficient energy transfer from Ce3+ to Tb3+ ions in CYHA, the CYHA:Ce3+,Tb3+ samples presented a wide excitation band in the 370–470 nm region peaking around 408 nm owing to the 4f–5d transition of Ce3+ ions, and under 408 nm excitation they showed intense characteristic sharp green emission around 543 nm corresponding to the 5D4 → 7F0–6 transitions of Tb3+ ions. The energy transfer mechanism from Ce3+ to Tb3+ ions was ascribed to the quadruple–quadruple interaction, and the energy transfer efficiency reached as high as 93.2%. Notably, the composition-optimized CYHA:0.03Ce3+,0.6Tb3+ sample exhibited a high internal quantum efficiency (IQE) of 78.5% and external quantum efficiency (EQE) of 56%, which were much higher than those of the Tb3+ singly-activated CYHA:0.6Tb3+ sample (IQE = 8%, EQE = 2.2%). Finally, a prototype white LED device was made by combining a 400 nm near-UV-emitting LED chip with a phosphor blend of the as-prepared CYHA:0.03Ce3+,0.6Tb3+ green phosphors, commercial BaMgAl10O17:Eu2+ blue phosphors and commercial CaAlSiN3:Eu2+ red phosphors, which emitted bright warm-white light with good CIE chromaticity coordinates of (0.391, 0.356), a low correlated color temperature of 3528 K and a high color rendering index of 92.3 under 120 mA driving current. This work opens up new opportunities for the development of efficient color converters toward near-UV-pumped warm-white LEDs with high color rendering index.

Highly efficient near-UV-excitable Ca2YHf2Al3O12:Ce3+,Tb3+ green-emitting garnet phosphors with potential application in high color rendering warm-white LEDs

With admirable luminescence performance and a cheap price, non-rare-earth-based oxide red phosphors are a potential competitor of rare-earth-doped phosphors for warm white LEDs (WLEDs). Herein, a novel double-perovskite Ba2GdSbO6:Mn4+ phosphor, demonstrating strong red emission ascribed to a spin-forbidden Mn4+:2Eg → 4A2g transition in the region of 620-750 nm, has been synthesized via a solid-state reaction route. The microstructure and luminescence properties are investigated in detail. The concentration quenching mechanism and thermal stability based on thermal quenching characteristics are also discussed. Importantly, Li+, Mg2+, Zn2+, Si4+, Ti4+ and Ge4+ dopants are discovered to be beneficial for enhancing Mn4+ luminescence, and the related mechanisms are comprehensively described. In addition, by combining red-emitting Ba2GdSb0.994O6:0.003Mn4+,0.003Mg2+ with the commercial blue-emitting BaMgAl10O17:Eu2+ and green-emitting Ba3La6(SiO4)6:Eu2+ phosphors in various ratios, a series of WLED devices with a tunable correlated color temperature (CCT) evolving from 6256 to 3486 K and a color rendering index (CRI) increasing from 72.1 to 88.3 are achieved.

Enhanced luminescence of a Ba2GdSbO6:Mn4+ red phosphor via cation doping for warm white light-emitting diodes.

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Enhanced luminescence of a Ba2GdSbO6:Mn4+ red phosphor via cation doping for warm white light-emitting diodes.