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(Sr1-xMex)2SiO4:Eu熒光粉光譜調(diào)控機(jī)制
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1.南昌大學(xué)材料科學(xué)與工程學(xué)院;2.南昌大學(xué)江西省輕質(zhì)高強(qiáng)結(jié)構(gòu)材料重點(diǎn)實(shí)驗(yàn)室

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國家重點(diǎn)研發(fā)計(jì)劃 (2016YFB0701203,2016YFB0701201,2017YFB1103701 )、國家自然科學(xué)基金 (11564025,51671101)、江西省教育廳重點(diǎn)計(jì)劃 (GJJ150010) 、南昌大學(xué)雙創(chuàng)及科研訓(xùn)練項(xiàng)目基金(CX2019052、20190402352)


Luminescent spetra regulation mechnism of (Sr1-xMex)2SiO4:Eu
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    摘要:

    采用高溫固相法制備(Sr1-xMex)1.95SiO4:0.05Eu系列熒光粉,研究不同大(Ba2+)、小(Mg2+)半徑離子基體固溶對(duì)其物相、發(fā)光中心配位結(jié)構(gòu)、Eu離子價(jià)態(tài)的影響,探究其光譜精細(xì)調(diào)控機(jī)制。Sr2SiO4粉末中隨著溫度升高α-Sr2SiO4相增加、β-Sr2SiO4相減少;Mg2+ (小半徑離子)摻雜可以提高α-Sr2SiO4相穩(wěn)定性,但容易出現(xiàn)Mg2SiO4,粉末中始終為混合物;Ba2+ (大半徑離子) 摻雜可以提高α-Sr2SiO4相穩(wěn)定性,粉體發(fā)生β-Sr2SiO4+α-Sr2SiO4→α-Sr2SiO4→α-Sr2SiO4+Ba2SiO4→Ba2SiO4轉(zhuǎn)變,且β-Sr2SiO4、α-Sr2SiO4、Ba2SiO4的順序其Si–O–Me(I)–O–Me(II)鏈逐漸由鋸齒狀變?yōu)槠街睜?、Me-O鍵長拉長。Eu離子激活的β-Sr2SiO4、α-Sr2SiO4、Ba2SiO4粉體在254nm(365nm) 激發(fā)下有明亮的綠色熒光發(fā)射(且依序強(qiáng)度增強(qiáng)、光譜整體略微藍(lán)移)和微弱的紅光發(fā)射;當(dāng)光學(xué)基體發(fā)生β-Sr2SiO4→α-Sr2SiO4轉(zhuǎn)變時(shí),發(fā)射光譜中Eu2+(I)藍(lán)移Eu2+(II)紅移(Si–O–Sr(I)–O–Sr(II)由鋸齒形鏈成為平鏈,且Sr-O鍵拉長),發(fā)生α-Sr2SiO4→Ba2SiO4轉(zhuǎn)變則Eu2+(I)、Eu2+(II)均發(fā)生藍(lán)移(僅發(fā)生Me-O鍵拉長);三種粉體熱釋光譜中均存在Eu2+和Eu3+缺陷能級(jí),且Eu2+缺陷濃度更高。Eu3d的精細(xì)x射線光電子譜表明隨著β-Sr2SiO4→α-Sr2SiO4→Ba2SiO4轉(zhuǎn)變其Eu離子以Eu2+存在的可能性增大,對(duì)應(yīng)的電子順磁共振也證實(shí)這一結(jié)果。由此可見,采用Ba2+離子固溶摻雜Sr2SiO4,可在一定濃度范圍得到單相粉末,實(shí)現(xiàn)光學(xué)基體的β-Sr2SiO4→α-Sr2SiO4→Ba2SiO4相變,調(diào)控Si–O–Me(I)–O–Me(II)鏈型及Me-O鍵長,調(diào)節(jié)Eu離子價(jià)態(tài)和配位場,進(jìn)而實(shí)現(xiàn)其綠色熒光粉熒光強(qiáng)度、發(fā)射波段精確調(diào)控。

    Abstract:

    The (Sr1-xMex)1.95SiO4:0.05Eu phosphor powders were synthesized by high temperature solid-state reaction. The effects of solid solution of different large (Ba2+) and small (Mg2+) ionic on the phase, the coordination crystal structure and the valence state of Eu ions were investigated firsly, and then regulation mechanism in the luminscent spectra was disccused. With increasing temperature, α-Sr2SiO4 increases and β-Sr2SiO4 phase decreases in Sr2SiO4 powder. Mg2+ ion dopant would increase the stability of α-Sr2SiO4 phase. Ba2+ ion dopant would lead the phase tranformation as β-Sr2SiO4+α-Sr2SiO4→α-Sr2SiO4→α-Sr2SiO4+Ba2SiO4→Ba2SiO4, in the sequence as β-Sr2SiO4, α-Sr2SiO4, Ba2SiO4, the Si–O–Me(I)–O–Me(II) chain changes from zigzag to straight chain, and the Me-O length increases. Under the excitation of 254nm (365nm), Eu-activated β-Sr2SiO4, α-Sr2SiO4, and Ba2SiO4 powders have bright green fluorescence emission (in the same sequence, the intensity increases and the overall spectrum is slightly blue shifted) and weak red light emission. For β-Sr2SiO4 →α-Sr2SiO4, Eu (I) emission peak is blue-shifted while the one of Eu (II) is red-shifted (Si–O–Me(I)–O–Me(II) chain changes from zigzag to straight, Me-O length increases). For α -Sr2SiO4 →Ba2SiO4, both emission peaks of Eu (I) and Eu (II) are blue-shifted (Me-O bond is enlonged). In the thermoluminescence spectra, there exit Eu2+ and Eu3+ defect energy levels in all these phosphors, and Eu2+ concentration looks larger. The high resolution XPS spectrum of Eu3d indicates that there are higher possibilities for Eu2+ in the sequence as β-Sr2SiO4 → α-Sr2SiO4 → Ba2SiO4, which is confirmed by Eu ion ESR spetra. By Ba2+ ions solid solution into Sr2SiO4 crystal, phase transforamtion as β-Sr2SiO4 → α-Sr2SiO4 → Ba2SiO4 would occurs, which would means the adjustmens in Si–O–Me(I)–O–Me(II) chain type and Me-O bond length. These would lead to the regulation in the coordination environment and valence state (Eu2+/ Eu3+ ratio) of Eu ion, and result to regular in emission wavelength and intensity.

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引用本文

汪雨,羅嵐,郭銳,張澎鵬,高明遠(yuǎn).(Sr1-xMex)2SiO4:Eu熒光粉光譜調(diào)控機(jī)制[J].稀有金屬材料與工程,2021,50(1):153~159.[Wang Yu, Luo Lan, Guo Rui, Zhang Peng Peng, Gao Ming Yuan. Luminescent spetra regulation mechnism of (Sr1-xMex)2SiO4:Eu[J]. Rare Metal Materials and Engineering,2021,50(1):153~159.]
DOI:10.12442/j. issn.1002-185X.20200013

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  • 收稿日期:2020-01-06
  • 最后修改日期:2020-02-10
  • 錄用日期:2020-02-21
  • 在線發(fā)布日期: 2021-02-05
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