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1.
Coordinationpolymersareofgrowinginterestin viewoftheirpotentialapplicationincatalysis,mo lecularrecognition,sensors,storagedevicesandso on[1~3].Asamultifunctionalligand,benzenedicar boxylicacid(H2BDC)hasbeenextensivelyusedin thesynthesisofcoordinationp…  相似文献   
2.
应用原位化学复合方法,将Eu^3+、Tb^3+与,1,10-邻菲罗啉配合光学均匀复合到SiO2凝胶玻璃中,解决了国稀土含氮配合物易水解而难以用溶胶-凝胶工艺将其均匀掺入无机基质的问题。研究了原位配合物的荧光和热学性能。结果表明,由于配合物的形成使稀土离子特征荧光强度显著增加,而无机基质的保护作用则使原位配合物热稳性提高200℃以上。化学合成纯配合物Eu(Phen)2Cl3·2H2O的高分辨荧光谱表  相似文献   
3.
采用Sol-Gel溶胶—凝胶的方法制备出了掺杂C  相似文献   
4.
Er3+掺杂的 MFT玻璃材料2H11/24S3/24I15/2荧光性质   总被引:2,自引:0,他引:2  
计算了Er  相似文献   
5.
用分子束外延生长了不同组分x的Zn1-xMnxSe外延膜和Zn1-xMnxSe/ZnSe超晶格.由于Zn1-xMnxSe的能隙Eg随组分变化在低组分区形成弓形,且弓形的范围随温度变化的反常特性,首次在光致发光谱(PL)中观测到当温度升高时,Zn1-xMnxSe/Znse超晶格中由ZnSe为阱、Zn1-xSe为垒转换成Zn1-xSe为阱,ZnSe为垒.瞬态光致发光结果表明,Zn1-xMnxSe/ZnSe超晶格中Mn++离子的激发态弛豫时间远大于Zn1=xMnxSe外延模中Mn++离子的弛豫时间,这可能是由于  相似文献   
6.
Increases of emission intensities for Eu^3 at the S6 site relative to that at the C2 site were observed as UV excitation wavelength decreases from 300 nm to 200 nm in both bulk and nanocrystalline cubic Y2O3:Eu^3 . Decomposition of excitation spectra shows that the charge transfer band of Eu^3 at the S6 site lies in the high-energy side of that at the C2 site, resulting in that the energy transfer from the host prefers to the S6 site. Detailed emission and excitation spectral characteristics were analyzed and discussed. In addition, spectral red-shift were found in both charge transfer bands in nanocrystalline Y2O3: Eu^3 compared to the bulk material. The number ratio of S6 sites to C2 sites is also smaller in nanocrystalline Y2O3:Eu^3 than that in the bulk one.  相似文献   
7.
Itiswellknownthatreductionofparticlesizeofcrystallinesystemcanresultinremarkablemodifica tionoftheirpropertieswhicharedifferentfromthoseofbulkbecauseofhighsurfacetovolumeratioandquan tumconfinementeffectofnanometermaterials .In1994 ,Bhargavaetal .reportedthatradiativetransi tionrateofMn2 ionsinZnSnanocrystalincreasedsixorderincomparisonwithbulkone[1] .Despitethisre sultwasstronglycriticizedlater ,studiesonnanosizedluminescentsemiconductorattractedgreatinter ests[2~ 4 ] .Sincecompoundsofra…  相似文献   
8.
SpectralHoleBurningandPhoto-StimulatedLuminescenceProcessesinBaF(Cl,Br):Sm~(2+)SongHongwei(宋宏伟);ZhangJiahua(张家骅);LuShaozhe(吕少?..  相似文献   
9.
A Series of niobate-silicate glasses doped with Eu3 ions were prepared. The emission, phonon-side band spectra, fluorescence line narrowing spectroscopy and fluorescence lifetimes in these glasses were studied. The intensity parameters and crystal field parameter of Eu3 were obtained. The results indicate that the intensity ratio of the electric-dipole to magnetic-dipole transition and the intensity parameter Ω2 increase with the increasing concentration of Nb2Os, indicating that the symmetry becomes lower, the Eu-O bonds become stronger and the covalency of Eu-O bond increases. The value of B20 decreases with the increasing concentration of Nb2O5, indicating that the distance between the Eu3 ion and oxygen decreases and the Eu-O bond becomes strong, corresponding to the results of the former. As the concentration of Nb2O5 increases, the electron-phonon coupling becomes stronger, thus the nonradiative transition rate of 5Do becomes larger and the lifetime of 5D0 becomes shorter.  相似文献   
10.
Nanoparticles and nanowires of LAPO4: Eu phosphors were synthesized by hydrothermal method. Their luminescent properties including electronic transition, surface effect, and temperature-dependent luminescent characteristics were systemically studied and compared to the bulk powders. It can be concluded that in comparison with the bulk powders, the fluorescence intensity decreases in nanoparticles and nanowires, while the lifetime increases, indicating that the radiative transition rate decreases. The nonradiative transition rate in nanowires decreases than that in nanoparticles due to its decreased surface to volume ratio. The temperature-dependent experiments indicate that the thermal quenching in nanopowders becomes weaker than that in the bulk powders.  相似文献   
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