| In this work,phosphors of Mn2+and Mn4+doped yttrium aluminum garnet and yttrium orthoaluminate were synthesized by a traditional solid-state reaction method.The composition,morphology and luminescence properties of samples were investigated by XRD,SEM and spectrofluorometer.The excitation wavelength,emission wavelength,fluorescence decay etc of Mn2+and Mn4+dopant ions in the host were studied as well as luminescent tunability has been investigated.Furthermore,the effective application in white light LED,temperature sensor and so on were explored.(1)The Ce3+/Mn2+/Si4+:Y3Al5O122 phosphors were synthesized by a traditional solid-state reaction and they have intense red luminescence attributed to Mn2+:4T1→6A1 spin-forbidden transition under the excitation of blue light via efficient energy transfer from Ce3+to Mn2+.Temperature-dependent emission spectra and luminescent decay curves evidenced that Mn2+activators partitioned into both the Al3+octahedral site and Y3+dodecahedral one while Si4+ones located in the Al3+tetrahedral site as charge compensators.Furthermore,inorganic Ce3+:Y3Al5O12and Ce3+/Mn2+/Si4+:Y3Al5O122 dual-phase transparent glass ceramics were successfully fabricated by a low-temperature co-sintering technique to replace phosphor in organic silicone as color converter,and the red to yellow tunable luminescence can be easily achieved via controlling the content of red phosphor in glass matrix.Notably,by combining the fabricated dual-phase glass ceramics with InGaN blue chip,warm white light-emitting diodes with superior optical performance and excellent heat-resistance stability were successfully constructed.(2)A series of Mn4+doped Y3-y(Gd/Lu)yAl5-xGaxO12(x=05;y=03)phosphors were fabricated by a conventional high-temperature solid-state reaction technique.In this work,taking Y3Al5O12as the Mn4+doped host,we demonstrate the tunability of excitation and emission of Mn4+activator via cation substitution.X-ray diffraction patterns confirm that Y3+and Al3+in the host can be completely replaced by Gd3+/Lu3+and Ga3+,respectively.Impressively,the substitution of Al3+ions by Ga3+ones is beneficial to significantly enhance Mn4+4A2→4T2 blue excitation band and shift 2E→4A2 red emission band toward low-energy region.the replacement of Y3+by Gd3+induces red-shifting of both Mn4+excitation and emission bands while Lu3+doping leads to the opposite result.Finally,inorganic Ce3+:Y3Al5O12and Mn4+:Y3Al5O122 dual-phase embedded glass ceramic is prepared by a low-temperature co-sintering route to replace phosphors in organic silicone as color converter,and by combiningthe synthesized glass ceramic with InGaN blue chip,warm white light-emitting diode with superior optical performance is successfully realized.(3)A novel Yb3+/Ln3+/Mn4+(Ln=Er,Ho,Tm):YAlO3 phosphors were fabricated by a conventional high temperature solid-state reaction.In the present work,a strategy to achieve Mn4+room-temperature near-infrared upconversion luminescence with the aid of efficient energy transfer of Yb3+→Ln3+→Mn4+in the specially prepared Yb3+/Ln3+/Mn4+(Ln=Er,Ho,Tm):YAlO3 products is reported for the first time.Steady-state and time-resolved upconversion emission spectra are adopted to systematically clarify the related energy transfer mechanisms and determine energy transfer efficiencies.Benefited from completely different thermal-quenching mechanisms of Mn4+and Ln3+as well as intermediate crystal field environment of Mn4+in YAlO3 host,the possibility using Mn4+/Ln3+dual-emitting based upconversion fluorescence intensity ratio and Mn4+upconversion lifetime as dual-modal temperature signals for accurate temperature sensing is demonstrated.It is believed that this preliminary study will offer a significant advance in exploring novel transitional metal based upconversion materials as well as self-calibrated optical thermometric media. |