Generally,
crystal field engineering is an important means to regulate
Cr3+ luminescence in near-infrared (NIR) phosphors. Host
cation substitutions, including single substitutions, double substitutions,
and even multiple substitutions, are widely used as a common means
to modify the crystal field of Cr3+-activated phosphors.
However, the tunable range using this strategy is usually limited
because it is susceptible to the limitation of the host and its initial
structure. In this work, we designed and synthesized a new type of
controllable NIR-emitting phosphor Li2Mg3TiO6:Cr3+ using a new Cr3+ luminescent ion
substitution strategy in which a double Cr3+ ion unit [Cr3+–Cr3+] was employed to replace a [Mg2+–Ti4+] unit to balance the charge. Just
by changing the concentration of Cr3+, the NIR emission
peak of the phosphor can be regularly adjusted from 720 to 920 nm,
and the full width at half maximum reaches 258 nm. The internal quantum
efficiency and external quantum efficiency of the Li2Mg3TiO6:0.03Cr3+ sample are measured to
be 72.1 and 28.1%, respectively. An NIR phosphor-converted light-emitting
diode (pc-LED) is fabricated by the LMT:Cr3+ phosphor and
a blue chip, and the radiant fluxes of 31.09 mW@(3 V ∼ 100
mA) and 71.56 mW@(3 V ∼ 420 mA) are achieved. The results confirmed
that the luminescence material has great application potential in
the field of NIR spectroscopy.