Near-infrared (NIR) persistent luminescence (PersL) materials are attractive multifunctional-material-platforms to real-time-required studies and applications in chemistry and biomedicine. However, the inefficient charging by low-irradiance, noncoherent, and high-tissue-penetration red–NIR light restricts their developments and applications in situ, such as long-term tracking, whole-body, and deep-tissue bioimaging. To address this issue, we develop a novel Cr 3+ -activated Na 0.5 Gd 0.5 TiO 3 NIR-PersL material with perovskite structure. It shows over 100 times stronger PersL intensity than those of the best known Cr 3+ -doped phosphors, including ZnGa 2 O 4, Zn 3 Ga 2 GeO 8, Zn 3 Ga 2 Ge 2 O 10, and LiGa 5 O 8, with low-irradiance (∼2.5 μW·mm –2 ) and noncoherent red light (laser-free) charging. Based on the structural and spectroscopic studies, we reveal a novel one-photon charging mechanism in the constructed host referred binding energy (HRBE) schemes, which differs from the regular two-photon one of those Cr 3+ -doped gallates. The host conduction band minimum (CBM) plays a critical factor in the charging efficiency and the charging-required photon numbers. Tissue-penetration verification and in vivo bioimaging demonstrated the potentials of realizing renewed and high signal-to-noise ratio (SNR) in situ imaging with low-irradiance (∼19 μW·mm –2 ) and noncoherent red–NIR charging. The one-photon charging concept will contribute to the new mechanism to guide the design of the high-tissue-penetration NIR-PersL imaging probes with laser-free and low-irradiance red–NIR excitation.
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Huang et al. (2020) studied this question.
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