Do triboluminescence spectra really show a spectral shift relative to photoluminescence spectra?

Duignan, J.P.; Oswald, Iain D. H.; Sage, Ian; Sweeting, Linda M.; Tanaka, Katsuhisa; Ishihara, T.; Hirao, Kazuyuki; Bourhill, Grant

doi:10.1016/s0022-2313(01)00412-4

Cited by 59 publications

(30 citation statements)

References 29 publications

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“…Rare earths can be doped into BSAS to produce luminescence, with the rare earth presumably substituting on the Ba 2+ /Sr 2+ sites (46,47) considering ionic radii, although solubility is expected to be limited. Divalent rare earths, notably Sm 2+ , Eu 2+ , and Yb 2+ , are easily formed by reducing atmospheres in BaAl 2 Si 2 O 8 (48)(49)(50).…”

Section: Other Silicatesmentioning

confidence: 99%

Doped Oxides for High-Temperature Luminescence and Lifetime Thermometry

Chambers

Clarke

2009

Annu. Rev. Mater. Res.

253

143

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The measurement of high temperatures in oxides and oxide-based structures in practical applications often presents challenges including steep thermal gradients, the presence of flames or chemically aggressive environments, and the transparency or translucency of most oxides. For turbine engines, oxide coatings are of great commercial importance, and the rapid motion of parts prohibits contact thermometry. Luminescence thermometry offers a number of advantages for measuring temperature in such systems and has been the subject of ongoing study for many years. Recent work on rareearth-doped thermal barrier coatings, environmental barrier coatings, and related oxides has demonstrated the feasibility of luminescence thermometry to temperatures well in excess of 1000 • C. The luminescent properties of these materials and the analytical techniques used to extract reproducible temperature measurements from the measured luminescence are reviewed. 325 Annu. Rev. Mater. Res. 2009.39:325-359. Downloaded from www.annualreviews.org by University of Wisconsin -Madison on 09/25/12. For personal use only.

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Section: Other Silicatesmentioning

confidence: 99%

Doped Oxides for High-Temperature Luminescence and Lifetime Thermometry

Chambers

Clarke

2009

Annu. Rev. Mater. Res.

253

143

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“…Several origins have been suggested to explain such spectral differences between ML and PL: self-absorption of ML light, pressureinduced changes of the Franck-Condon factors, and generation of different excited-states by fracture-induced symmetry changes in applying strong pressures [13,14]. The self-absorption of ML light is not likely to occur in 2 and 3 as judged by their large Stokes shift in solution ($100 nm) (Fig.…”

Section: IImentioning

confidence: 99%

“…5). It is also expected that the pressureinduced changes of Franck-Condon factors could be small in 2 and 3 presumably due to the long emission lifetime ($ls, Table 2) compared with the very short duration of applying pressures ($ps) [13].…”

Section: IImentioning

confidence: 99%

Group 4 ansa-metallocenes derived from o-carborane and their luminescent properties

Shin¹,

Han²,

Lee³

et al. 2009

Journal of Organometallic Chemistry

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“…[19] In the case of ZnS:Mn, there are six transitions in the excitation spectrum: 349, 392, 429, 465, 498 and 535 nm. [20] Recrystallization of NHEt 3 Eu(dbm) 4 opens the possibility to control the size of the crystals. The size of the triboluminescent materials is important because of several reasons: first of all the crystal size has a strong impact onto the mechanical properties of the resulting hybrid materials.…”

Section: Triboluminescent Materialsmentioning

confidence: 99%

Functional Diblock Copolymers for the Integration of Triboluminescent Materials into Polymer Matrices

Meuer

Zentel

2008

Macro Chemistry & Physics

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This work describes the synthesis and use of new diblock copolymers to integrate functional inorganic particles into a polymer matrix. These diblock copolymers were synthesized by nitroxide‐mediated polymerization (NMP) from styrene and two styrene‐like monomers with protected functional groups for the later connection to the functional inorganic material. It was possible to keep the polydispersity of the block copolymers around or below 1.2 and to preset the length of the functional block to about 20 monomers or 10 mol‐% of monomers. The groups for the surface functionalization (amino groups or chelating ligands) were obtained in their free form by polymer analogous reactions. As an example of functional inorganic materials, two highly triboluminescent materials were synthesized and investigated: an europium complex that is sensitive to fracture only and a manganese‐doped zinc sulfide that is also sensitive to reversible deformations. The interaction of the functional block copolymers with these triboluminescent crystals could be proved by (i) selective adsorption on surfaces coated with the block copolymer, (ii) by copolymer‐mediated transfer of the crystals from water to a chloroform phase and (iii) by the homogenous embedding of the crystals in a polystyrene (PS) matrix.

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Do triboluminescence spectra really show a spectral shift relative to photoluminescence spectra?

Cited by 59 publications

References 29 publications

Doped Oxides for High-Temperature Luminescence and Lifetime Thermometry

Doped Oxides for High-Temperature Luminescence and Lifetime Thermometry

Group 4 ansa-metallocenes derived from o-carborane and their luminescent properties

Functional Diblock Copolymers for the Integration of Triboluminescent Materials into Polymer Matrices

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