Electrochemistry c - v method was employed to measure the carrier concentration profile distribution of samples , discovered that the carrier concentration decreased with increasing of the diffusion depth , and the peak of concentration located at 0 . 25 m beneath the surface 利用電化學(xué)c - v法對樣品的載流子濃度的縱向分布進(jìn)行了研究,發(fā)現(xiàn)在距離樣品表面0 . 25 m處載流子濃度達(dá)到最大。
Based on a chloride concentration test of field - exposed concrete specimens , a numerical example is given . the result shows that the chloride concentration increases with service time , decreases with diffusion depth , and the chloride diffusivity is a variable with time , depth and chloride concentration 通過對自然環(huán)境中混凝土試件的現(xiàn)場氯離子濃度試驗的算例分析發(fā)現(xiàn),混凝土中的氯離子濃度隨服役時間增加而增加,隨擴(kuò)散深度的增加而減少。
Moreover , we observed the concentration profiles of the ion - implanted samples and the diffused samples by c - v method , and discovered that the carrier concentration decreased with increasing of the diffusion depth . whereas , the peak concentration of the ion - implanted samples located at 0 . 248151 u m beneath the surface and the peak concentration of the diffused samples located at the surface . furthermore , the carrier concentration of mnas source diffused sample as high as 102 % m3can be obtained , and the surface was much smoother compared with that of the pure mn source diffused sample 發(fā)現(xiàn)兩種摻雜方法的載流子濃度大體上都是隨著擴(kuò)散深度的增加而下降,不同的是離子注入樣品的載流子最高濃度處于離表面深度0 . 248151 m處,而擴(kuò)散樣品的載流子最高濃度處于表面,并摻錳( mn )砷化鋅( gaas )材料性質(zhì)的研究且還發(fā)現(xiàn)相對于純mn源擴(kuò)散樣品來說, mnas源擴(kuò)散樣品的表面較為光滑,且表面載流子濃度高達(dá)1020 cm ’數(shù)量級。