稀有金属材料与工程
稀有金屬材料與工程
희유금속재료여공정
RARE METAL MATERIALS AND ENGINEERNG
2009年
z2期
275-278
,共4页
陈燕%江向平%郑雪娟%涂娜%冯子义%陈超%李月明
陳燕%江嚮平%鄭雪娟%塗娜%馮子義%陳超%李月明
진연%강향평%정설연%도나%풍자의%진초%리월명
Co_2O_3掺杂%K_0.5Na_0.5NbO_3%压电性能%介电性能
Co_2O_3摻雜%K_0.5Na_0.5NbO_3%壓電性能%介電性能
Co_2O_3참잡%K_0.5Na_0.5NbO_3%압전성능%개전성능
Co_2O_3-doping%K_0.5Na_0.5NbO_3%piezoelectric properties%dielectric properties
采用固相反应法制备了K_0.5Na_0.5NbO_3+xCo_2O_3(0≤x≤1%)无铅压电陶瓷,使用XRD、SEM、 Agilent 4294A精密阻抗分析仪等对该体系的相组成、显微结构、压电及介电等性能进行表征.结果表明:Co_2O_3的掺入并没有改变K_0.5Na_0.5NbO_3的晶体结构,该陶瓷材料仍然为正交相钙钛矿结构;Co_2O_3的掺入使材料的晶粒尺寸明显增大,但当x=1%时,晶粒尺寸减小,说明过多的Co_2O_3有抑制晶粒长大的作用;Co_2O_3的掺入使200 ℃附近的正交→四方铁电相变温度TO-T向低温方向移动,居里温度TC向高温方向移动,同时材料的压电常数d_(33)、机电耦合系数k_p均随之先增大后减小,机械品质因数Qm整体增大,1 kHz频率下的介电常数ε_r和介电损耗tanδ降低,密度显著增大.当x=0.5%时,陶瓷性能最佳:d_(33)=103 pC/N,k_p=0.362, tanδ=1.8%,ε_r=234,Qm=182,ρ=4.29 g/cm~3.
採用固相反應法製備瞭K_0.5Na_0.5NbO_3+xCo_2O_3(0≤x≤1%)無鉛壓電陶瓷,使用XRD、SEM、 Agilent 4294A精密阻抗分析儀等對該體繫的相組成、顯微結構、壓電及介電等性能進行錶徵.結果錶明:Co_2O_3的摻入併沒有改變K_0.5Na_0.5NbO_3的晶體結構,該陶瓷材料仍然為正交相鈣鈦礦結構;Co_2O_3的摻入使材料的晶粒呎吋明顯增大,但噹x=1%時,晶粒呎吋減小,說明過多的Co_2O_3有抑製晶粒長大的作用;Co_2O_3的摻入使200 ℃附近的正交→四方鐵電相變溫度TO-T嚮低溫方嚮移動,居裏溫度TC嚮高溫方嚮移動,同時材料的壓電常數d_(33)、機電耦閤繫數k_p均隨之先增大後減小,機械品質因數Qm整體增大,1 kHz頻率下的介電常數ε_r和介電損耗tanδ降低,密度顯著增大.噹x=0.5%時,陶瓷性能最佳:d_(33)=103 pC/N,k_p=0.362, tanδ=1.8%,ε_r=234,Qm=182,ρ=4.29 g/cm~3.
채용고상반응법제비료K_0.5Na_0.5NbO_3+xCo_2O_3(0≤x≤1%)무연압전도자,사용XRD、SEM、 Agilent 4294A정밀조항분석의등대해체계적상조성、현미결구、압전급개전등성능진행표정.결과표명:Co_2O_3적참입병몰유개변K_0.5Na_0.5NbO_3적정체결구,해도자재료잉연위정교상개태광결구;Co_2O_3적참입사재료적정립척촌명현증대,단당x=1%시,정립척촌감소,설명과다적Co_2O_3유억제정립장대적작용;Co_2O_3적참입사200 ℃부근적정교→사방철전상변온도TO-T향저온방향이동,거리온도TC향고온방향이동,동시재료적압전상수d_(33)、궤전우합계수k_p균수지선증대후감소,궤계품질인수Qm정체증대,1 kHz빈솔하적개전상수ε_r화개전손모tanδ강저,밀도현저증대.당x=0.5%시,도자성능최가:d_(33)=103 pC/N,k_p=0.362, tanδ=1.8%,ε_r=234,Qm=182,ρ=4.29 g/cm~3.
The K_0.5Na_0.5NbO_3 +xwt%Co_2O_3(0≤x≤1)lead-free piezoelectric ceramics were fabricated by solid state reaction. The phase, microstructure, electric properties of the samples were characterized by XRD, SEM and Agilent 4294A impedance analyzer. With the increasing of Co_2O_3 content, all samples have an orthorhombic perovskite structure and the grain size of those materials increases obviously with the increase of Co_2O_3 content. However, when x=1, the grain size decreases, which indicates that more Co_2O_3 content can inhibit the grain growth. And the transitional temperature around 200 ℃ (TO-T, from orthorhombic to tetragonal phase) will shift to lower temperature, while the Curie temperature (T_C) will shift to higher temperature. Furthermore, the piezoelectric constant (d_(33)), electromechanical planar coupling coefficients (k_p) increased firstly and decreased subsequently with the increase of content of Co_2O_3. The mechanical quality factor (Q_m) increases evidently. The dielectric constant (ε_r) and dielectric loss (tgδ) decreases, and the density increases. When x equals to 0.5, it exhibits optimal piezoelectric properties: d_(33)=103pC/N, k_p=0.362, tanδ=1.8%, ε_r=234, Q_m=182 and ρ=4.29 g/cm~3.