Transactions of Nonferrous Metals Society of China The Chinese Journal of Nonferrous Metals

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中國有色金屬學(xué)報

ZHONGGUO YOUSEJINSHU XUEBAO

第18卷    第8期    總第113期    2008年8月

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文章編號:1004-0609(2008)08-1492-06
共沉淀法制備BaHfO3׃Ce納米粉體及發(fā)光性能
劉 晶1, 3,馬偉民1,聞 雷2,李喜坤3,沈世妃4 郭易芬4

(1. 沈陽化工學(xué)院 材料科學(xué)與工程學(xué)院,沈陽 110142;
2. 中國科學(xué)院金屬研究所 沈陽材料科學(xué)國家(聯(lián)合)實驗室,沈陽 110016;
3. 沈陽理工大學(xué) 材料工程學(xué)院,沈陽 110168;
4. 沈陽大學(xué) 材料科學(xué)與工程系,沈陽 110044
)

摘 要: 研究以草酸和氨水作為沉淀劑制備BaHfO3׃Ce納米粉體的工藝。用XRDTEM等測試技術(shù),分析不同沉淀劑對粉體合成中的物相變化、形貌及Ce3+摻雜量對粉體激發(fā)光譜和發(fā)射光譜的影響。結(jié)果表明:以氨水做沉淀劑在900 ℃煅燒2 h合成的BaHfO3׃Ce粉體形貌近似球形,平均粒徑約15 nm。用草酸做沉淀劑、合成溫度為1 000 ℃時其粉體形貌呈多邊形,粒徑約60 nm。微量Ce3+的摻雜不改變BaHfO3的晶體結(jié)構(gòu)。Ce3+摻雜量(摩爾分?jǐn)?shù))0.3%BaHfO3發(fā)射光譜相對峰強(qiáng)度最高,當(dāng)Ce3+摻雜量大于0.3%時出現(xiàn)濃度淬滅現(xiàn)象。粉體的激發(fā)和發(fā)射光譜均存在較寬的譜帶,主要由激活Ce3+5d→2F5/25d→2F7/2寬帶能級躍遷產(chǎn)生。

 

關(guān)鍵字: BaHfO3׃Ce粉體;共沉淀法;Ce3+摻雜量;光譜特性

Preparation and spectrum characteristics of BaHfO3׃Ce nano-powder by co-precipitation
LIU Jing1. 3, MA Wei-min1, WEN Lei2, LI Xi-kun3, SHEN Shi-fei4, GUO Yi-fen4

1. School of Materials Science and Engineering, Shenyang Institute of Chemical Technology, Shenyang 110142, China;
2. Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences,Shenyang 110016, China;
3. School of Materials and Engineering, Shenyang Technology University, Shenyang 110168,China;
4. Department of Materials Science and Engineering, Shenyang University, Shenyang 110044, China

Abstract: The processing technology of Ce doped-BaHfO3 nano-powders that is prepared by co-precipitation (with oxalic acid and ammonia as the precipitant, respectively) was investigated. XRD and TEM were employed to analyze the effects of different precipitates on the phase change, morphologies of powders and influences of Ce3+ dopant content on the excitation and emission spectra of powders. The results show that spherical BaHfO3׃Ce nano-powders are synthesized only at 900 ℃ for 2 h and the average diameter is about 15 nm with ammonia as precipitant. But using oxalic acid as precipitant, the powders have polygonal morphology after calcining at 1 000 ℃ for 2 h and the average diameter is about 60 nm. Minor Ce3+ has no effect on the crystal structure. The relative intensity of photoluminescence peak has the maximum value when the Ce3+ dopant content is 0.3% (mole fraction). The concentration quench occurs when the Ce3+ dopant content exceeds 0.3%. The emission character is resulted from 5d→2F5/2 and 5d→2F7/2 transitions of Ce3+ and both the excitation and emission spectra are wide band.

 

Key words: BaHfO3׃Ce powder; co-precipitation; Ce3+ dopant content; spectrum characteristics

ISSN 1004-0609
CN 43-1238/TG
CODEN: ZYJXFK

ISSN 1003-6326
CN 43-1239/TG
CODEN: TNMCEW

主管:中國科學(xué)技術(shù)協(xié)會 主辦:中國有色金屬學(xué)會 承辦:中南大學(xué)
湘ICP備09001153號 版權(quán)所有:《中國有色金屬學(xué)報》編輯部
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