In recent years, rare-earth-doped
nanophosphors have attracted
great attention in the field of luminescent materials for advanced
solid-state lighting and high-resolution display applications. However,
the low efficiency of concurrent red phosphors creates a major bottleneck
for easy commercialization of these devices. In this work, intense
red-light-emitting K
+
-codoped BaAl
2
O
4
:Eu
3+
nanophosphors having an average crystallite size
of 54 nm were synthesized via a modified sol–gel method. The
derived nanophosphors exhibit strong red emission produced by the
5
D
0
→
7
F
J
(
J
= 0, 1, 2, 3, 4) transitions of Eu
3+
upon UV and low-voltage electron beam excitation. Comparative photoluminescence
(PL) analysis is executed for Eu
3+
-activated and K
+
-coactivated BaAl
2
O
4
:Eu
3+
nanophosphors, demonstrating remarkable enhancement in PL intensity
as well as thermal stability due to K
+
codoping. The origin
of this PL enhancement is also analyzed from first-principles calculations
using density functional theory. Achievement of charge compensation
with the addition of a K
+
coactivator plays an important
role in increasing the radiative lifetime and color purity of the
codoped nanophosphors. Obtained results substantially approve the
promising prospects of this nanophosphor in the promptly growing field
of solid-state lighting and field emission display devices.