中国有色金属学报
中國有色金屬學報
중국유색금속학보
THE CHINESE JOURNAL OF NONFERROUS METALS
2014年
1期
221-228
,共8页
李晏平%刘志宏%李玉虎%刘智勇%李启厚
李晏平%劉誌宏%李玉虎%劉智勇%李啟厚
리안평%류지굉%리옥호%류지용%리계후
In2O3%SnO2%烧结行为
In2O3%SnO2%燒結行為
In2O3%SnO2%소결행위
In2O3%SnO2%sintering behavior
采用XRD、SEM和XRF等表征方法研究In2O3、SnO2及其混合粉(In2O3与SnO2质量比为9:1)在N2、空气及O2气氛下于1300~1600℃烧结过程中的粉末分解质量损失、反应固溶、新相生成及孔洞形成等行为,以期为高密度铟锡氧化物(ITO)靶材制备奠定基础。结果表明:在1300~1600℃高温烧结中,In2O3和SnO2均分解升华, SnO2较In2O3更易于分解,增大烧结气氛的氧分压,有利于抑制分解反应的发生;在O2气氛下,ITO粉在1500℃开始显著分解产生质量损失;ITO粉在N2、空气和O2气氛中于1300℃下烧结4 h,样品中均存在SnO2相;于1400℃下烧结4 h,SnO2相消失,In4Sn3O12相出现;随着烧结温度的进一步升高,In4Sn3O12分解消失,其分解温度随烧结气氛氧分压增大而提高;在O2气氛下烧结,所得ITO粉晶格常数最低,且较为稳定,颗粒收缩较均匀,有利于高密度ITO靶材制备。
採用XRD、SEM和XRF等錶徵方法研究In2O3、SnO2及其混閤粉(In2O3與SnO2質量比為9:1)在N2、空氣及O2氣氛下于1300~1600℃燒結過程中的粉末分解質量損失、反應固溶、新相生成及孔洞形成等行為,以期為高密度銦錫氧化物(ITO)靶材製備奠定基礎。結果錶明:在1300~1600℃高溫燒結中,In2O3和SnO2均分解升華, SnO2較In2O3更易于分解,增大燒結氣氛的氧分壓,有利于抑製分解反應的髮生;在O2氣氛下,ITO粉在1500℃開始顯著分解產生質量損失;ITO粉在N2、空氣和O2氣氛中于1300℃下燒結4 h,樣品中均存在SnO2相;于1400℃下燒結4 h,SnO2相消失,In4Sn3O12相齣現;隨著燒結溫度的進一步升高,In4Sn3O12分解消失,其分解溫度隨燒結氣氛氧分壓增大而提高;在O2氣氛下燒結,所得ITO粉晶格常數最低,且較為穩定,顆粒收縮較均勻,有利于高密度ITO靶材製備。
채용XRD、SEM화XRF등표정방법연구In2O3、SnO2급기혼합분(In2O3여SnO2질량비위9:1)재N2、공기급O2기분하우1300~1600℃소결과정중적분말분해질량손실、반응고용、신상생성급공동형성등행위,이기위고밀도인석양화물(ITO)파재제비전정기출。결과표명:재1300~1600℃고온소결중,In2O3화SnO2균분해승화, SnO2교In2O3경역우분해,증대소결기분적양분압,유리우억제분해반응적발생;재O2기분하,ITO분재1500℃개시현저분해산생질량손실;ITO분재N2、공기화O2기분중우1300℃하소결4 h,양품중균존재SnO2상;우1400℃하소결4 h,SnO2상소실,In4Sn3O12상출현;수착소결온도적진일보승고,In4Sn3O12분해소실,기분해온도수소결기분양분압증대이제고;재O2기분하소결,소득ITO분정격상수최저,차교위은정,과립수축교균균,유리우고밀도ITO파재제비。
The sintering behaviors, such as the decomposition and mass loss, reactive solid solution, generation of new phases and holes of In2O3 and SnO2 as well as their mixed (mass ratio of In2O3 to SnO2 9:1) powders, were studied in the temperature range of 1 300~1 600℃under the atmospheres of N2, air and O2 by means of characterization methods of XRD, SEM, XRF, and so on, in order to lay the foundation for preparing high density ITO targets. The results show that, during the sintering processes in the temperature range of 1 300~1 600℃, both In2O3 and SnO2 may decompose and sublime. Compared to In2O3, SnO2 powders are easier to decompose, increasing oxygen partial pressure of the sintering atmosphere is beneficial to inhibiting their decompositions, and under O2 atmosphere, ITO powders begin to decompose and lose mass until as high as 1 500℃. After sintering under atmospheres of N2, air and O2 for 4 h, SnO2 still exists in ITO powders at 1 300℃, and at 1 400℃, phase SnO2 will disappear with the formation of a new phase, In4Sn3O12. With the further increase of sintering temperature, phase In4Sn3O12 will disappear, and the higher the oxygen partial pressure of the sintering atmosphere is, the higher the temperature is, in which phase In4Sn3O12 disappears. In case of sintering under O2 atmosphere, the lattice parameters of ITO powders obtained are the lowest and more stable, and moreover, the particle shrinkage during sintering is also more uniform, which are beneficial to preparing high density ITO targets.