功能材料
功能材料
공능재료
Journal of Functional Materials
2015年
17期
17076-17081
,共6页
麦海翔%谢致薇%徐继承%胡典禄%杨元政%陈先朝%何玉定
麥海翔%謝緻薇%徐繼承%鬍典祿%楊元政%陳先朝%何玉定
맥해상%사치미%서계승%호전록%양원정%진선조%하옥정
CuAlO2%稀土掺杂%相结构%光电性能
CuAlO2%稀土摻雜%相結構%光電性能
CuAlO2%희토참잡%상결구%광전성능
CuAlO2%rare-earth-doped%phase structure%photoelectric performance
采用柠檬酸络合的无机盐溶胶‐凝胶法制备稀土掺杂铜铁矿结构的CuAlO2粉末,掺杂元素M 为稀土Eu、Nd、Y。用DSC‐TGA、X射线衍射仪、紫外‐可见光分光光度计等测试方法分别对掺杂 CuAl1- x M x O2粉末的形成过程、物相结构、光学性能等进行研究。结果表明,稀土掺杂前驱体粉末经950℃煅烧后形成CuAlO2相;经1100℃保温4 h的煅烧后,粉末相组成取决于稀土掺杂量,当稀土元素M (Eu、Nd和Y)的掺杂量为0.5%时,试样由CuAlO2主相和少量CuO杂相组成,当掺杂量≥1%时,由CuAlO2主相、少量CuO 和 M AlO3杂相组成,YAlO3杂相峰强度较低。提高煅烧温度有利于掺杂元素的溶入,生成CuAl1- x M x O2纯相,但提高到1150℃时CuAlO2分解;Eu掺杂量<1%时,掺杂样品光学带隙增大,电阻率减小,光电性能得到改善。
採用檸檬痠絡閤的無機鹽溶膠‐凝膠法製備稀土摻雜銅鐵礦結構的CuAlO2粉末,摻雜元素M 為稀土Eu、Nd、Y。用DSC‐TGA、X射線衍射儀、紫外‐可見光分光光度計等測試方法分彆對摻雜 CuAl1- x M x O2粉末的形成過程、物相結構、光學性能等進行研究。結果錶明,稀土摻雜前驅體粉末經950℃煅燒後形成CuAlO2相;經1100℃保溫4 h的煅燒後,粉末相組成取決于稀土摻雜量,噹稀土元素M (Eu、Nd和Y)的摻雜量為0.5%時,試樣由CuAlO2主相和少量CuO雜相組成,噹摻雜量≥1%時,由CuAlO2主相、少量CuO 和 M AlO3雜相組成,YAlO3雜相峰彊度較低。提高煅燒溫度有利于摻雜元素的溶入,生成CuAl1- x M x O2純相,但提高到1150℃時CuAlO2分解;Eu摻雜量<1%時,摻雜樣品光學帶隙增大,電阻率減小,光電性能得到改善。
채용저몽산락합적무궤염용효‐응효법제비희토참잡동철광결구적CuAlO2분말,참잡원소M 위희토Eu、Nd、Y。용DSC‐TGA、X사선연사의、자외‐가견광분광광도계등측시방법분별대참잡 CuAl1- x M x O2분말적형성과정、물상결구、광학성능등진행연구。결과표명,희토참잡전구체분말경950℃단소후형성CuAlO2상;경1100℃보온4 h적단소후,분말상조성취결우희토참잡량,당희토원소M (Eu、Nd화Y)적참잡량위0.5%시,시양유CuAlO2주상화소량CuO잡상조성,당참잡량≥1%시,유CuAlO2주상、소량CuO 화 M AlO3잡상조성,YAlO3잡상봉강도교저。제고단소온도유리우참잡원소적용입,생성CuAl1- x M x O2순상,단제고도1150℃시CuAlO2분해;Eu참잡량<1%시,참잡양품광학대극증대,전조솔감소,광전성능득도개선。
The powders of rare earth element M (Eu ,Nd ,Y) doped CuAlO2 were synthesized by inorganic sol‐gel method .Formation process of doped CuAlO2 ,phase structure ,optical properties were studied by DSC‐TGA ,X‐ray diffraction and UV‐Vis spectrophotometer .The results showed that the rare earth doped CuAlO2 phase can be formed at 950 ℃ .After treated at 1 100 ℃ for 4 h ,phase composition of the powders was depend‐ent on doping content .The 0 .5% doped powder was composed of main phase CuAlO2 and a small amount of CuO phase .When the doping content was greater than or equal to 1% ,the doped powder was composed of main phase CuAlO2 ,a small amount of CuO and MAlO3 phase .Diffraction peak intensity of YAlO3 phase was the lowest among EuAlO3 ,NdAlO3 and YAlO3 phase .Higher treatment temperature was favorable to solution into the CuAlO2 lattice of the doping elements and formation of CuAl1 - x M x O2 phase .CuAlO2 decomposes at 1 150 ℃ .When the doping content of Eu was less‐then 1% ,The optical band gap increased ,the resistivity de‐creased and the photoelectric performance improvemented .