1997
DOI: 10.1023/a:1018525728259
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Cited by 7 publications
(4 citation statements)
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“…The PL intensity fell off to 19% by further heating to 300 °C, while it recovered completely the initial value upon cooling, showing the high thermal stability of the host lattice itself. By considering the high lattice rigidity (i.e., low thermal expansion , ) and the consequent smaller Stokes shift (SS) in the current system, the observed thermal quenching might mainly result from the ionization of excited 5d electron of Eu 2+ into the conduction band, caused by the remarkable decrease of the E g value. The occurrence of photoionization is also suggested by the decreased emission efficiency under the excitation below ∼350 nm region, as indicated by the PL excitation spectrum shown in Figure .…”
Section: Resultsmentioning
confidence: 93%
“…The PL intensity fell off to 19% by further heating to 300 °C, while it recovered completely the initial value upon cooling, showing the high thermal stability of the host lattice itself. By considering the high lattice rigidity (i.e., low thermal expansion , ) and the consequent smaller Stokes shift (SS) in the current system, the observed thermal quenching might mainly result from the ionization of excited 5d electron of Eu 2+ into the conduction band, caused by the remarkable decrease of the E g value. The occurrence of photoionization is also suggested by the decreased emission efficiency under the excitation below ∼350 nm region, as indicated by the PL excitation spectrum shown in Figure .…”
Section: Resultsmentioning
confidence: 93%
“…Such α-SiAlON ceramics are thermally durable. 9,10 In recent years, they have been used as phosphors with luminescence corresponding to rare-earth ions such as Eu 2+ , Tb 3+ , Yb 2+ , and Er 3+ . [11][12][13][14][15] Because solitary Ce 3+ does not stabilize α-SiAlON, co-doping with stabilizing ions such as Ca 2+ , Y 3+ , and Lu 3+ is performed to obtain α-SiAlON phosphors activated by Ce 3+ .…”
mentioning
confidence: 99%
“…A common way to increase the oxidation resistance of Mo or Mo-based alloys is to protect the surface by deposition of [106] Al 2 O 3 8.6 [107] B 5.0-7.0 [108] CaMoO 4 13.5/22.8 (*) a) [109] CMAS 9.8 [110] Cr 10.8 [111] CrN 7.16 [112] CrSi 2 16.8/10.9(*) a) [113] Gd 2 Zr 2 O 7 12.4 [114] Mo 5.7 [115] Mo 2 B 5.0 [116] Mo 2 B 5 8.6 [116] Mo 2 N 6.7 [117] Mo 3 Si 7.2 [118] Mo 5 Si 2.97 B 0.16 5.7/13.9 (*) a) [28] Mo 5 Si 3 11.8/5.8 (*) a) [7] Mo 5 SiB 2 7.55 [57] MoB 8.4/6.4 (*) a) [118] MoB 2 7.7 [116] MoSi 2 8.0/10.0 (*) a) [28] Mo-Si-B 5.0-6.0 [28] PHPS (pyrolyzed) 3-4 [86,88] Si 2.6 [119] SiB 6 5.1 [120] SiC 5.1 [121] Si 3 N 4 3.6 [122] SiO 2 0.5-4.1 [28] Steel (fcc) 17 [123] Ti 10.5 [124] TiN 11.0 [125] W 4.6 [126] YSZ 11.7 [127] a)…”
Section: Metallic Coatingsmentioning
confidence: 99%