电化学
電化學
전화학
2000年
4期
399-405
,共7页
程璇%刘峰名%林昌健%温作新%田中群%薛茹
程璇%劉峰名%林昌健%溫作新%田中群%薛茹
정선%류봉명%림창건%온작신%전중군%설여
多孔硅%光致发光%表面形貌
多孔硅%光緻髮光%錶麵形貌
다공규%광치발광%표면형모
Porous silicon%Photoluminescence%Surface morphology
本工作通过采用电化学极-化学氧化两步法在1:1氢氟酸和乙醇溶液中制备出孔径约为1~2 μm,厚度大经为6~10 μm的多孔硅样品.首先将0.03 A/cm2的恒电流施加到p(100)硅片一段时间,然后将该硅片浸到20%的硝酸溶液中氧化一段时间.通过此方法获得的多孔硅结构再进一步用扫描电子显微镜和拉曼光谱仪进行表面形貌和光学性质的考察.所有制备出的多孔硅结构均有光致发光现象.老化的多孔硅样品(在干燥器放置一年)的光致发光谱峰强度明显增强,但分别经过苯乙烯和十六碳烯(1)两种有机溶剂处理1 h后的老化多孔硅样品的光致发光强度却没有显著改变.
本工作通過採用電化學極-化學氧化兩步法在1:1氫氟痠和乙醇溶液中製備齣孔徑約為1~2 μm,厚度大經為6~10 μm的多孔硅樣品.首先將0.03 A/cm2的恆電流施加到p(100)硅片一段時間,然後將該硅片浸到20%的硝痠溶液中氧化一段時間.通過此方法穫得的多孔硅結構再進一步用掃描電子顯微鏡和拉曼光譜儀進行錶麵形貌和光學性質的攷察.所有製備齣的多孔硅結構均有光緻髮光現象.老化的多孔硅樣品(在榦燥器放置一年)的光緻髮光譜峰彊度明顯增彊,但分彆經過苯乙烯和十六碳烯(1)兩種有機溶劑處理1 h後的老化多孔硅樣品的光緻髮光彊度卻沒有顯著改變.
본공작통과채용전화학겁-화학양화량보법재1:1경불산화을순용액중제비출공경약위1~2 μm,후도대경위6~10 μm적다공규양품.수선장0.03 A/cm2적항전류시가도p(100)규편일단시간,연후장해규편침도20%적초산용액중양화일단시간.통과차방법획득적다공규결구재진일보용소묘전자현미경화랍만광보의진행표면형모화광학성질적고찰.소유제비출적다공규결구균유광치발광현상.노화적다공규양품(재간조기방치일년)적광치발광보봉강도명현증강,단분별경과분을희화십륙탄희(1)량충유궤용제처리1 h후적노화다공규양품적광치발광강도각몰유현저개변.
Porous silicon structures were formed by a two-step technique consisting of electrochemical polarization and chemical oxidation processes in 1∶1 hydrofluoric acid and ethanol solutions. A constant current density of 0.03 A/cm2 was applied to p-type silicon wafers, followed by chemical treatment in 20% nitric acid solutions. These samples were then carefully examined by scanning electron microscope (SEM) and Raman spectrometer to study their surface morphologies and optical properties. After a year storage in a desiccator, the aged porous silicon samples were re-examined by SEM and Raman spectrometer before and after treated with styrene and decene(1) organic solvents, respectively. It was found that the Raman intensities of the aged porous silicon samples were significantly enhanced. However, the treatments of the aged porous silicon samples with tow organic solvents did not alter their optical properties.