The N
3–
-substituted
Li
2
MSiO
4
:Eu
2+
(M = Ca, Sr, and Ba)
phosphors were systematically
prepared and analyzed. Secondary-ion mass spectroscopy measurements
revealed that the average N
3–
contents are 0.003
for Ca, 0.009 for Sr, and 0.032 for Ba. Furthermore, the N
3–
incorporation in the host lattices was corroborated by infrared
and X-ray photoelectron spectroscopies. From the photoluminescence
spectra of Li
2
MSiO
4
:Eu
2+
(M = Ca,
Sr, and Ba) phosphors before and after N
3–
doping,
it was verified that the enhanced emission intensity of the phosphors
is most likely due to the N
3–
doping. In Li
2
MSiO
4
:Eu
2+
(M = Ca, Sr, and Ba) phosphors,
the maximum wavelengths of the emission band were red-shifted in the
order Ca < Ba < Sr, which is not consistent with the trend of
crystal field splitting: Ba < Sr < Ca. This discrepancy was
clearly explained by electron–electron repulsions among polyhedra,
LiO
4
–MO
n
, SiO
4
–MO
n
, and MO
n
–M’O
n
associated
with structural difference in the host lattices. Therefore, the energy
levels associated with the 4f
6
5d energy levels of Eu
2+
are definitely established in the following order: Li
2
CaSiO
4
:Eu
2+
> Li
2
BaSiO
4
:Eu
2+
> Li
2
SrSiO
4
:Eu
2+
. Furthermore, using the Williamson–Hall (W–H)
method, the determined structural strains of Li
2
MSiO
4
:Eu
2+
(M = Ca, Sr, and Ba) phosphors revealed that
the increased compressive strain after N
3–
doping
induces the enhanced emission intensity of these phosphors. White
light-emitting diodes made by three N
3–
-doped phosphors
and a 365 nm emitting InGaN chip showed the (0.333, 0.373) color coordinate
and high color-rendering index (
R
a
= 83).
These phosphor materials may provide a platform for development of
new efficient phosphors in solid-state lighting field.