Development of highly thermally stable broadband near-infrared
(NIR) luminescence materials is crucial for advancing the prolonged
stable application of smart NIR light sources. In this study, a zero-thermal-quenching
and reversible temperature-dependent broadband NIR-emitting Cs2NaAl3F12:Cr3+ phosphor is
demonstrated, benefiting from its stable polyhedron-cluster-building
rigid structure. The excellent thermal stability of Cs2NaAl3F12:Cr3+ is rooted in its stable
[Al6Na4F45] cluster building unit,
which provides a rigid structure with a weak electron–phonon
coupling effect and a wide band gap with a huge thermal activated
barrier. Such characteristics are well revealed by multiple studies
on crystal structure, electronic structure, Huang–Rhys factor S, configuration coordinate model, and Debye temperature.
The incorporation of Li or K instead of Na weakens the luminescence
thermal stability, directly proving the importance of the stable [Al6Na4F45] cluster for stable Cr3+ substitution and rigid structure construction. Furthermore, Cs2NaAl3F12:Cr3+ presents much
superior thermal stability compared to traditional rigid garnet-type
fluorides Na3X2Li3F12:Cr3+ (X = Al, Ga, In). A high-power NIR LED is presented, utilizing
the high quantum efficiency (∼71%) and extremely thermally
stable broadband NIR emission around 750 nm of Cs2NaAl3F12:Cr3+. It realizes clear vein and
cartilage imaging in the human hand, demonstrating its potential in
medical diagnosis applications. This result provides important insights
for designing new-type rigid crystal structures using stable polyhedron
clusters as basic units, advancing the development of highly thermally
stable NIR-emitting phosphors.