Developing high-color-quality white light-emitting diodes
(LEDs)
is crucial for energy-efficient light bulbs and modern flat panel
displays. Creating the luminescent phosphors that enable these advanced
lighting technologies requires stable photoluminescence under varying
temperatures. In this study, we examine Ba2Ca2B4O10 substituted with Ce3+, which
emits an efficient blue-cyan light (λem ≈
455 nm and a quantum yield of 74%) that is required for high color
rendering lighting. Synchrotron powder X-ray diffraction and optical
spectroscopy reveal that the broad emission band is attributed to
Ce3+ ions occupying two crystallographically independent
Ba2+ positions in the host crystal structure. However,
temperature-dependent luminescence measurements unveil a surprising
phenomenon: a significant blue shift (from 460 to 415 nm) accompanied
by a drastic narrowing of the total emission bandwidth (from 140 nm,
6900 cm–1 to 58 nm, and 3200 cm–1). This extreme optical response arises from two simultaneous thermal
quenching mechanismssite preferential quenching and high thermal
expansion (αV ≈ 5.39 × 10–5 K–1). Consequently, the phosphor experiences a
chromatic shift that transforms a fabricated prototype light bulb’s
perceived color from functional white light to an undesirable yellow-green
hue. These findings underscore the considerable impact of chromatic
instabilities in phosphors and the effects they can have on the performance
of LED lighting.