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Ho~(3+)/Yb~(3+)∶8YSZ纳米粉体制备及发光性能研究
引用本文:罗军明,曹志超,邓莉萍,徐吉林.Ho~(3+)/Yb~(3+)∶8YSZ纳米粉体制备及发光性能研究[J].人工晶体学报,2017(10).
作者姓名:罗军明  曹志超  邓莉萍  徐吉林
作者单位:南昌航空大学材料科学与工程学院,南昌,330063
基金项目:国家自然科学基金(51362022),江西省自然科学基金重大项目(20152ACB2013)
摘    要:通过化学共沉淀法制备Ho~(3+)/Yb~(3+)共掺杂的氧化钇稳定的氧化锆(8YSZ)纳米粉体。研究了煅烧温度对Ho~(3+)/Yb~(3+)共掺杂8YSZ纳米粉体荧光光谱和上转换发光性能的影响。结果表明:在448 nm波长激发光激发下,Ho~(3+)/Yb~(3+)∶8YSZ纳米粉体有一个549 nm的绿光发射峰,随着煅烧温度的升高,Ho~(3+)/Yb~(3+)∶8YSZ纳米粉体的荧光强度先升高后降低。980 nm波长激光激发下,Ho~(3+)/Yb~(3+)∶8YSZ纳米粉体在450~750 nm范围内有一个中心波长在539 nm的绿光发射峰和一个中心波长在650 nm的红光发射峰,随着煅烧温度的升高,纳米粉体的颗粒尺寸增大的同时,其上转换发光强度也逐渐增大。

关 键 词:Ho3%2B/Yb3%2B:8YSZ纳米粉体  化学共沉淀法  荧光光谱  上转换发光  煅烧温度

Preparation and Luminescence Property of Ho3+/Yb3 +:8YSZ Nanopowders
LUO Jun-ming,CAO Zhi-chao,DENG Li-ping,XU Ji-lin.Preparation and Luminescence Property of Ho3+/Yb3 +:8YSZ Nanopowders[J].Journal of Synthetic Crystals,2017(10).
Authors:LUO Jun-ming  CAO Zhi-chao  DENG Li-ping  XU Ji-lin
Abstract:Ho3 +/Yb3 + co-doped yttria-stabilized zirconia ( 8YSZ ) nano powders were prepared by chemical coprecipitation .The effect of calcination temperatures on the fluorescence spectra and up-conversion luminescence properties of the Ho 3+/Yb3+co-doped nano 8YSZ was investigated .The results show that the Ho 3+/Yb3 +co-doped 8YSZ nano powders have a green emission peak at 549 nm under excitation of the 448 nm wavelength excitation light .The luorescence intensity of the Ho 3+/Yb3+ co-doped 8 YSZ nanopowders increases first , and then decreases with increasing the calcination temperatures.Under excitation of the 980 nm wavelength laser , the Ho3+/Yb3+ co-doped 8YSZ nanopowders have a green emission peak at a central wavelength of 539 nm and a red emission peak at a central wavelength of 650 nm in the range of 450-750 nm.With increasing the calcination temperatures , the particle sizes of the nano powders increase and the upper conversion luminescence intensity also gradually increases .
Keywords:Ho3+/Yb3+:8YSZ nanopowder  chemical coprecipitation  fluorescence spectra  upconversion luminescence  calcination temperature
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