Mechanoluminescence (ML) phosphors have made significant
progress
in various fields, such as artificial intelligence, the Internet of
Things, and biotechnology. However, enhancing their weak ML intensity
still remains a challenge. Here, we report a new series of Na1–x
Mg
x
NbO3:Pr3+ (x = 0.00, 0.10, 0.20, 0.40,
0.60, 0.80, and 1.00 mol %) heterojunction systems, which exhibit
significant ML enhancement as compared with either the Pr3+-doped NaNbO3 or MgNbO3, and the physical mechanisms
behind the ML enhancement have been explored comprehensively from
both the experiment and theory points of view. Experimental tests,
including thermoluminescence and positron annihilation lifetime measurements,
combined with first-principles calculations, consistently indicate
that the ML enhancement observed in these newly reported systems is
due to the formation of heterojunctions, which plays a crucial role
in modulating the defect configuration of the phosphors and facilitating
efficient charge transfer. By controlling the Na/Mg ratio in conjunction
with Pr3+ doping, continuous changes in the band offset
and the concentrations of certain types of traps in the forbidden
gap are achieved, leading to the optimum conditions in the 8/2 ratio
samples. These findings demonstrate a novel type of ML phosphor and
provide a theoretical basis for the design of high-performance ML
phosphor.