This study presents an approach for synthesizing Eu2+/Eu3+-coactivated Ca2SiO4 nanophosphors,
by adjusting the ratio of both activators within a singular host material.
Utilizing a hydrothermal method complemented by a postreduction sintering
process, we fabricated a series of phosphors characterized by uniform
30–50 nm spherical nanoparticles. These engineered phosphors
manifest multichannel luminescence properties and exhibit simultaneous
blue and red emission from Eu2+ and Eu3+, respectively.
Meticulous control of the 5% H2–95% N2 reduction temperature allowed for precise tuning of the Eu2+ and Eu3+ ions within the host lattice, which enabled
the strategic adjustment of their luminescent outputs. Utilizing X-ray
photoelectron spectroscopy (XPS), we could discern subtle alterations
in the europium oxidation state. By using a transmission electron
microscope (TEM) and an X-ray diffractometer (XRD), we found that
the subsequent changes by reductive sintering to particle
size, morphology, and mixed crystal structures influenced the materials’
luminescent characteristics. Our findings herald a significant advancement
in solid-state lighting, with the potential for the use of Eu2+/Eu3+-coactivated calcium silicate nanophosphors
to develop white light emission technologies endowed with enhanced
color rendering and luminous efficacy.