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3篇 您的检索式:作者名="K.Sajeev"
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1New constraints on the P-T path of HT/UHT metapelites from the Highland Complex of Sri Lanka显示文摘We report here rare evidence for the early prograde P-Tevolution of garnet-sillimanite-graphite gneiss(khondalite)from the central Highland Complex,Sri Lanka.Four types of garnet porphyroblasts(Grt_1,Grt_2,Grt_3 and Grt_4)are observed in the rock with specific types of inclusion features.Only Grt_3 shows evidence for non-coaxial strain.Combining the information shows a sequence of main inclusion phases,from old to young:oriented quartz inclusions at core,staurolite and prismatic sillimanite at mantle,kyanite and kyanite pseudomorph,and biotite at rim in Grt_1;fibrolitic sillimanite pseudomorphing kyanite±corundum,kyanite,and spinel+sillimanite after garnet+corundum in Grt_2;biotite,sillimanite,quartz±spinel in Grt_3;and ilmenite,rulite,quartz and sillimanite in Grt_4.The pre-melting,original rock composition was calculated through stepwise re-integration of melt into the residual,XRF based composition,allowing the early prograde metamorphic evolution to be deduced from petrographical observations and pseudosections.The earliest recognizable stage occurred in the sillimanite field at around 575℃ at 4.5 kbar.Subsequent collision associated with Gondwana amalgamation led to crustal thickening along a P-T trajectory with an average dP/dT of ~30 bar/℃ in the kyanite field,up to ~660℃ at 6.5 kbar,before crossing the wet-solidus at around 675 ℃ at 7.5 kbar.The highest pressure occurred at P > 10 kbar and T around 780℃ before prograde decompression associated with further heating.At 825℃ and 10.5 kbar,the rock re-entered into the sillimanite field.The temperature peaked at 900℃ at ca.9-9.5 kbar.Subsequent near-isobaric cooling led to the growth of Grt_4 and rutile at T ~880℃.Local pyrophyllite rims around sillimanite suggest a late stage of rehydration at T<400℃,which probably occurred after uplift to upper crustal levels.U-Pb dating of zircons by LAICPMS of the khondalite yielded two concordant ^(206)Pb/^(238)U age groups with mean values of 542±2 Ma(MSWD=0.24,Th/U=0.01-0.03)and 514±3 Ma(MSWD=0.50,Th/U=0.01-0.05)interpreted as peak metamorphism of the khondalite and subsequent melt crystallization during cooling.P.L.Dharmapriya Sanjeewa P.K.Malaviarachchi L.M.Kriegsman Andrea Galli K.Sajeev Chengli Zhang 2017Geoscience Frontiers2017,8,6:2
2Distinct metamorphic evolution of alternating silica-saturated and silica-deficient microdomains within garnet in ultrahigh-temperature granulites: An example from Sri Lanka显示文摘Here we report the occurrence of garnet porphyroblasts that have overgrown alternating silica-saturated and silica deficient microdomains via different mineral reactions. The samples were collected from ultrahigh-temperature(UHT) metapelites in the Highland Complex, Sri Lanka. In some of the metapelites, garnet crystals have cores formed via a dehydration reaction, which had taken place at silicasaturated microdomains and mantle to rim areas formed via a dehydration reaction at silica-deficient microdomains. In contrast, some other garnets in the same rock cores had formed via a dehydration reaction which occurred at silica-deficient microdomains while mantle to rim areas formed via a dehydration reaction at silica-saturated microdomains. Based on the textural observations, we conclude that the studied garnets have grown across different effective bulk compositional microdomains during the prograde evolution. These microdomains could represent heterogeneous compositional layers(paleobedding/laminations) in the precursor sediments or differentiated crenulation cleavages that existed during prograde metamorphism. UHT metamorphism associated with strong ductile deformation, metamorphic differentiation and crystallization of locally produced melt may have obliterated the evidence for such microdomains in the matrix. The lack of significant compositional zoning in garnet probably due to self-diffusion during UHT metamorphism had left mineral inclusions as the sole evidence for earlier microdomains with contrasting chemistry.P.L.Dharmapriya Sanjeewa P.K.Malaviarachchi Leo M.Kriegsman K.Sajeev Andrea Galli Y.Osanai N.D.Subasinghe C.B.Dissanayake 2017Geoscience Frontiers2017,8,5:1
3Blue emitting exciplex for yellow and white organic light‑emitting diodes显示文摘White organic light-emitting diodes(WOLEDs)have several desirable features,but their commercialization is hindered by the poor stability of blue light emitters and high production costs due to complicated device structures.Herein,we investigate a standard blue emitting hole transporting material(HTM)N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)benzidine(NPB)and its exciplex emission upon combining with a suitable electron transporting material(ETM),3-(biphenyl-4-yl)-5-(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole(TAZ).Blue and yellow OLEDs with simple device structures are developed by using a blend layer,NPB:TAZ,as a blue emitter as well as a host for yellow phosphorescent dopant iridium(III)bis(4-phenylthieno[3,2-c]pyridinato-N,C2')acetylacetonate(PO-01).Strategic device design then exploits the ambipolar charge transport properties of tetracene as a spacer layer to connect these blue and yellow emitting units.The tetracene-linked device demonstrates more promising results compared to those using a conventional charge generation layer(CGL).Judicious choice of the spacer prevents exciton difusion from the blue emitter unit,yet facilitates charge carrier transport to the yellow emitter unit to enable additional exciplex formation.This complementary behavior of the spacer improves the blue emission properties concomitantly yielding reasonable yellow emission.The overall white light emission properties are enhanced,achieving CIE coordinates(0.36,0.39)and color temperature(4643 K)similar to daylight.Employing intermolecular exciplex emission in OLEDs simplifes the device architecture via its dual functionality as a host and as an emitter.Kavya Rajeev C.K.Vipin Anjali K.Sajeev Atul Shukla Sarah K.M.McGregor Shih‑Chun Lo Ebinazar B.Namdas K.N.Narayanan Unni 2023Frontiers of Optoelectronics2023,16,4:0
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