N. Galkin, D. T. Yan, K. Galkin, A. Nepomnyaschiy, D. Goroshko
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引用次数: 0
摘要
本文研究了室温下镍电沉积(Ni ED)时间(5,6,7,8分钟)和450℃氩气气氛下退火对介孔硅(meso-PS)及其Ni纳米复合材料(meso-PS/Ni)的结构、组成和发光性能的影响。SEM和EDX能谱数据表明,Ni在表面的浓度占主导地位,而在近表面区域的浓度不显著。根据拉曼和PL光谱数据,建立,倪艾德在NiCl2溶液后,氧化镍子(NiOx)的带隙2.8 e V meso-PS表层,形成,短期退火(5和6分钟)后,转换成一氧化镍纳米晶体(NiO),导致一个强大的(0.2 - 0.9 eV)“蓝色”转变的PL的最大(2.4 - -2.6 eV)纳米复合材料与meso-PS / Ni多个PL振幅增加。随着Ni ED时间的增加和在空气中的储存时间的增加,NiOx没有形成,并且检测到的PL振幅显著(2-18倍)增加,并伴有0.05-0.1 eV的小“红”移,这可能与在介观- ps矩阵中以Ni离子形式形成辐射复合中心有关。在这种情况下,在氩气中退火会导致PL强度的降低,而不会改变PL最大值。
Luminescent Properties of Nanocomposites Based on Porous Silicon, Nickel, and Nickel Oxide in the Photon Energy Range of 1.4 - 2.9 eV
This paper presents the results of studying the effect of time (5, 6, 7, and 8 minutes) of nickel electrodeposition (Ni ED) at room temperature and annealing at 450°C in an argon atmosphere on the structure, composition, and photoluminescent (PL) properties of mesoporous silicon (meso-PS) and its nanocomposite with Ni (meso-PS/Ni). The SEM and EDX spectroscopy data showed the predominant concentration of Ni on the surface and an insignificant concentration in the near-surface region of the meso-PS. According to Raman and PL spectroscopy data, it was established that after Ni ED in a NiCl2 solution, nickel sub oxide (NiOx) with a band gap of up to 2.8 e V is formed in the meso-PS surface layer, which, after short-term annealing (5 and 6 min), is transformed into nickel monoxide nanocrystals (NiO), which leads to a strong (0.2 - 0.9 eV) “blue” shift of the PL maximum (2.4-2.6 eV) of the nanocomposite with meso-PS/Ni with a multiple increase in the PL amplitude. With an increase in the time of Ni ED and storage in air, NiOx, is not formed, and the detected significant (2–18 times) increase in the PL amplitude with a small “red” shift of 0.05-0.1 eV is presumably associated with the formation of radiative recombination centers in the form of ions Ni in the meso-PS matrix. Annealing in argon in this case leads to a decrease in the PL intensity without shifting the PL maxima.