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Light-emitting properties of amorphous Si:C:O:H layers fabricated by oxidation of carbon-rich a-Si:C:H films

机译:通过富碳a-Si:C:H薄膜氧化制备的非晶Si:C:O:H层的发光特性

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Amorphous hydrogenated carbon-rich silicon-carbon alloy film (a-Si_(0.3C_(0.7): H) was deposited by reactive dc-magnetron sputtering of silicon target in argon-methane gas mixture. As-deposited film exhibits white photoluminescence at room temperature. After the deposition the samples were thermally annealed in dry Ar, wet Ar, or dry O_2 flow at 450 deg C for 30 minutes that resulted in the enhancement of the photoluminescence intensity by a factor of about 5, 8 and 12 respectively. Spectral distribution of light emission was almost unchanged at the annealing in dry and wet argon while the oxidation in pure oxygen resulted in strong enhancement of a "blue" shoulder in the spectrum. EPR measurements at room temperature showed the decrease of spin concentration after thermal treatment in dry and wet argon and no EPR signal was detected after annealing in oxygen. FTIR and XPS measurements evidenced the formation of a-Si:O:C:H composite material after dry oxidation. Based on the measurements of photoluminescence in the temperature range 7-300 K it is suggested that light-emitting efficiency of a-Si_(0.3)C_(0.7): H is determined by migration of the photo-excited carriers to non-radiative recombination centers. The physical mechanisms that can be involved in the strong enhancement of visible photoluminescence in Si:C:O:H layers are discussed.
机译:通过氩-甲烷混合气体中硅靶的反应性直流磁控溅射沉积非晶态氢化富碳硅碳合金膜(a-Si_(0.3C_(0.7):H),沉积的膜在室温下呈现白色光致发光在沉积之后,将样品在干燥的Ar,潮湿的Ar或干燥的O_2流中于450℃下进行30分钟的热退火,这导致光致发光强度分别提高了约5、8和12倍。在干和湿氩中退火时,发光分布几乎没有变化,而在纯氧中的氧化导致光谱中的“蓝”肩强烈增强;室温下的EPR测量表明,热处理后自旋浓度降低。干,湿氩在氧气中退火后均未检测到EPR信号,FTIR和XPS测量证明了干氧化后a-Si:O:C:H复合材料的形成。在7-300K的温度范围内的光致发光表明,a-Si_(0.3)C_(0.7):H的发光效率由光激发载流子迁移到非辐射复合中心决定。讨论了可能在Si:C:O:H层中强烈增强可见光致发光的物理机制。

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