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纳米银粒子表面包覆分子共振吸收峰的红移现象 总被引:5,自引:0,他引:5
本文首次发现了两种电性不同的染料分子若丹明6G及荧光素钠包覆纳米银粒子时,染料分子共振吸收峰的红移现象,以及产生红移的条件。前者只有在KC1、KBr、KI等电解质存在时才产生红移;而后者则无需这些电解质存在。其红移量分别为27um及13nm.并对产生红移的机理进行了讨论。 相似文献
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有机薄膜电致发光器件结构与发光特性的研究 总被引:4,自引:0,他引:4
从有机电致发光薄膜的发光机理出发,通过以Alq薄膜器件、PVK为空穴传输层和Alq为发光层的双层 及PVK掺荧光材料Perylene的双层薄膜器件的研制,从器件的电致姚谱、电流密度-电压特性、亮度-电压特性的曲线的测试结果,计算分析了器件的流明效率、量子效率,并对有机薄膜电致发光器件的结构与发光特性之间的关系进行研究,利用能级理论分析了器件的姚特性随器件的结构不同所具有的规律。实验表明,加入PVK 相似文献
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采用密度泛函(B3P86/6-311g**)方法研究了偶极电场作用下ZnO、ZnO 1和ZnO-1的几何结构、能级分布和激发态特性,得到了ZnO分子的Murrell-Sorbie解析势能函数及其相关光谱常数.计算结果表明,随偶极电场的增加,ZnO、ZnO 1和ZnO-1的轨道能隙减少,适当强度外电场作用下ZnO分子的激发能和紫外吸收光波波长与实验值吻合得很好,说明ZnO分子具有紫外受激发射的发光特性. 相似文献
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利用纳米银烧结工艺制备大功率LED,重点探究了纳米银键合层的界面热阻及器件发光性能。通过将纳米银膏在不同温度下烧结,系统地研究了烧结温度对纳米银烧结后电阻率及接头剪切强度的影响,并分析了烧结后银膏的晶体结构及接头断口微观形貌。结果表明,接头键合强度和银膜导电率均随纳米银烧结温度的升高而增大。实验中还对比分析了纳米银烧结LED和传统锡银铜(SAC305)焊膏封装LED的界面热阻、结温以及发光性能。与纳米银烧结LED样品相比,传统焊膏封装LED的界面热阻和结温分别提高了8.9%和29.6%,说明纳米银键合层拥有更好的导热性并可及时为芯片散热降温。此外,通过高温老化实验,深入探讨了不同焊膏烧结LED的界面热阻及发光效率变化。实验表明,经过100℃下点亮500 h,纳米银和传统焊膏烧结LED样品的总热阻分别增大了0.03 K/W和4.28 K/W,但纳米银键合层界面热阻比老化前有所降低,同时纳米银烧结LED样品在不同电流下的发光效率始终高于传统焊膏封装LED样品。 相似文献
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本文测量了GaP纯绿发光二极管在室温和液氮温度下的近红外发光光谱,观测到许多重叠的宽带发光.按高斯线型对光谱进行拟合,将其分解为6个发光谱峰,讨论了这些深能级发光的来源和它们对GaP发光二极管的发光强度的影响. 相似文献
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发光液晶材料的合成及发光特性研究 总被引:5,自引:1,他引:4
具有聚集诱导发光增强效应的发光液晶材料,能有效地解决一般发光材料聚集时荧光猝灭和液晶自组装之间的矛盾,在液晶显示等领域有极大的应用价值。本文报道了一种自发光液晶材料(2Z,2'Z)-2,2'-(1,4-亚苯基)二(3-(4-己氧基)苯基)丙烯腈(PHPA)。研究了PHPA的聚集态发光性质、溶剂化效应、热力学性质及发光各向异性。结果表明,PHPA同时具有聚集态诱导发光增强效应和液晶性,其有序取向的薄膜发出的光具有各向异性。该发光液晶材料应用于液晶显示将能简化器件结构、增加亮度、对比度和能效。 相似文献
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The optical properties of silver species in various oxidation and aggregation states and of tin centers in melt-quenched phosphate glasses have been assessed by optical absorption and photoluminescence (PL) spectroscopy. Glasses containing silver and tin, or either dopant, were studied. Emission and excitation spectra along with time-resolved and temperature-dependent PL measurements were employed in elucidating the different emitting centers observed and investigating on their interactions. In regard to silver, the data suggests the presence of luminescent single Ag+ ions, Ag+-Ag+ and Ag+-Ag0 pairs, and nonluminescent Ag nanoparticles (NPs), where Ag+-Ag0→Ag+-Ag+ energy transfer is indicated. Tin optical centers appear as twofold-coordinated Sn centers displaying PL around 400 nm ascribed to triplet-to-singlet electronic transitions. The optically active silver centers were observed in glasses where 8 mol% of both Ag2O and SnO, and 4 mol% of Ag2O were added. Heat treatment (HT) of the glass with the high concentration of silver and tin leads to chemical reduction of ionic silver species resulting in a large volume fraction of silver NPs and the vanishing of silver PL features. Further characterization of such heat-treated glass by transmission electron microscopy and X-ray photoelectron spectroscopy appears consistent with silver being present mainly in nonoxidized form after HT. On the other hand, HT of the glass containing only silver results in the quenching of Ag+-Ag0 pairs emission that is ascribed to nonradiative energy transfer to Ag NPs due to the positioning of the pairs near the surface of NPs during HT. In this context, an important finding is that a faster relaxation was observed for this nanocomposite in relation to a heat-treated glass containing both silver and tin (no silver pairs) as revealed by degenerate four-wave mixing spectroscopy. Such result is attributed to Ag NP→Ag+-Ag0 plasmon resonance energy transfer. The data thus indicates that energy transfer between Ag+-Ag0 pairs and NPs is bi-directional. 相似文献
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银纳米粒子与R6G分子间的电荷转移 总被引:8,自引:0,他引:8
本文通过吸收光谱、表面增强垃曼光谱、荧光光谱等手段研究了银纳米粒子与罗丹明6G(R6G)分子之间的相互作用,结果表明:银纳米粒子表面与R6G分子之间存在电荷转移效应。表现为吸收谱长波方向出现银粒子-R6G复合体的吸收带,R6G分子的拉曼振动模得到显著增强,而其荧光得到明显猝灭;AgN特征拉曼振动带的出现服银米粒子与R6G分子是通过银粒表面的活位与R6G分子中的氮原子配位形成复合体而发生电荷转移的。 相似文献
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Highly luminescent singles of Ag sol with gradual changes were detected when adjusting the granularity and concentration of particles. It can be deduced that these Ag sols, composed of a large amount of silver nanoparticles and clusters, may have their surface energy bands alterable, which might be caused by the interactions between particles. A model that describes the shift of energy band is proposed, and it can be understood as the hybridization of elementary plasmons when interactions occur between particles. Besides, both hybridization and absorption-rescattering mechanisms were proposed to explain the changeable phenomena of photoluminescence with different concentrations. 相似文献
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分别以柠檬酸钠(CTS)和聚乙烯吡咯烷酮(PVP)为表面修饰剂,采用化学法制备纳米银(分别标记为Ag-CTS和Ag-PVP)。当甲基橙溶液中加入Ag-CTS或Ag-PVP时,S2→S0和S1→S0荧光强度分别明显减弱和增强。不同的是Ag-PVP引起S2→S0和S1→S0荧光强度减弱和增强的幅度更大,且S2→S0荧光峰出现红移。当甲基橙溶液中加入Ag-CTS时,S1→S0荧光强度随时间延长逐渐增强,而加入Ag-PVP时,S1→S0荧光强度则不随时间而变化。颗粒尺寸较大的片状结构纳米银引起S1→S0荧光强度增强比率较小。甲基橙溶液浓度越低,S1→S0荧光强度增强比率越大。研究结果表明,纳米银表面吸附的不同表面修饰剂通过影响纳米银与甲基橙分子间距离进而影响纳米银的荧光增强效应;纳米银尺寸大小则由于所产生的局域面表面等离子共振特点等差异影响其局域场增强效应。 相似文献
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纳米银与表面吸附荧光素的荧光性能的影响 总被引:2,自引:0,他引:2
研究了纳米银粒子对表面吸附荧光素(fluorescein,Fl)的荧光性能的影响。Fl溶液中加入纳米银粒子,Fl分子包覆在纳米银粒子表面形成Fln-Ag复合物使纳米银相互桥连形成类似网络的结构,且Fl分子吸收峰随着纳米银浓度的增加发生红移。纳米银通过产生的强局域场将能量传输给Fl发光中心,实现了Fl的荧光增强,荧光增强效率随着纳米银浓度的增加具有最大值。较大粒径的纳米银使Fl获得最大荧光增强效率所需浓度较低且最大荧光增强效率值较高。研究结果表明,纳米银与Fl间的能量传输主要由Fl分子附近局域电磁场增强和分子到金属表面无辐射跃迁能量转移过程所决定并与纳米银的浓度、尺寸密切相关。 相似文献
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纳米银粒子对表面吸附罗丹明B的光谱学性质的影响及电解质效应研究 总被引:1,自引:1,他引:0
基于贵金属纳米粒子的局域场增强效应,利用透射电子显微镜、紫外-可见分光光度计和荧光分光光度计等分析手段研究了纳米银粒子对表面吸附罗丹明B的光谱学性质的影响以及罗丹明B-纳米银体系中加入电解质离子后,电解质离子与纳米银、染料分子间的相互关系和作用.研究结果表明,当罗丹明B溶液的浓度小于0.6 μmol·L-1时,微量纳米银可使其荧光强度略增加,继续增加纳米银浓度则造成荧光强度下降.当罗丹明B溶液的浓度高于0.6 μmol·L-1时,纳米银总是引起溶液的荧光强度下降.KNO3、KCl、Ca(NO3)2、MgCl2和CaCl2电解质可造成纳米银粒子不同程度的聚集和生长.引起的纳米银粒子的聚集程度关系为:CaCl2>MgCl2>KCl>Ca(NO3)2>KNO3.随着电解质加入量的增加,溶液的荧光强度先下降,而后又逐渐增强,直至达到定值.各电解质对罗丹明B-Ag溶液的荧光强度影响强弱关系为Ca(NO3)2>CaCl2>MgCl2>Cl>KNO3. 相似文献
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多方法制备纳米ZrO2及其光谱特性研究 总被引:3,自引:0,他引:3
利用水热法、醇热法、溶胶-凝胶法、微波法和超声法分别制备了纳米ZrO2。使用X射线(X-raydif-fraction)和荧光光谱(PL-Photoluminescence)对样品结构及发光特性进行了表征。不同方法制得稳定的四方相氧化锆纳米微粒,由X射线衍射(XRD)看出产物结晶良好,且粒径较小。测试样品的光致发光谱(PL),发现样品在254和412nm激发光激发时发光效率较高,可以观察到明显的红光和蓝光。对采用不同方法制备的样品,对其性质进行研究和比较。在固体发光特别是半导体发光理论基础上对氧化锆发光特性给出了一定解释,最后对纳米材料光学特性理论模型的建立进行了初步探讨。 相似文献
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Size effect of silver nano particles on the photophysical properties of 1,4-dihydroxy-2,3-dimethyl-9,10-anthraquinone (DHDMAQ)
have been investigated using optical absorption and fluorescence emission techniques. Silver nanoparticles of different sizes
have been prepared by Creighton method using magnetic stirrer and ultrasonic field. Quenching of fluorescence of DHDMAQ has
been found to increase with decrease in the size of the silver nanoparticles. Stern–Volmer quenching constants have also been
calculated. 相似文献