64 resultados para ZNSE


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The photoluminescence (PL) properties of ZnSe films grown by hot wall epitaxy are reported. The PL spectra show clear neutral donor-bound exciton peak; donor acceptor pair (DAP) peak, conduction band to acceptor (CA) peak, and their phonon replicas until fourth order. The conduction band to acceptor peak and it's phonon replicas exist until room temperature. From the ratio of PL intensities of DAP and CA peaks and their replicas, we obtain the Huang-Rhys factor S = 0.58, in agreement with other experiments for acceptor-bound exciton transitions. From the temperature dependence of PL intensities we derive the activation energy of thermal quenching process for the DAP transitions as about 7 meV.

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Pressure dependence of photoluminescence from ZnSe:Te-(CdSe)(1)(ZnSe)(3) short period superlattice quantum wells is reported. In addition to the exciton band from the superlattice layers, strong bands for localized excitons self-trapped al single Te (Te-1) atom, double Te atoms (Te-2) and Te clusters (Te-n, n greater than or equal to 3) as well as for the free excitons in isoelectronic Te incorporated ZnSe layers are observed. Significant differences in the pressure and temperature dependencies of the observed exciton transitions are presented and discussed.

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分别应用光致发光、电容-电压和深能级瞬态傅里叶谱技术说细研究ZnSe自组织量子点样品的光学和电学行为。光致发光温度关系表明ZnSe量子点的光致发光热猝火过程机理。两步猝火过程的理论较好模拟和解释了相关的实验数据。电容-电压测量表明样品表观载流子积累峰出现的深度(样品表面下约100nm处)大约是ZnSe量子点层的位置。深能级瞬态傅里叶谱获得的ZnSe量子点电子基态能级位置为ZnSe导带下的0.11eV,这与ZnSe量子点光致发光热猝火模型得到的结果一致。

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测量了ZnSe_(0.92)Te_(0.08)/ZnSe超晶格量子阱材料在77K时0~7.8GPa静压下的光致发光谱。观察到AnSe_(0.92)Te_(0.08)阱层中Te等电子陷阱上的束缚激子发光,发现它的压力系数比ZnSe带边发光的压力系数小约50%,表明Te等电子陷阱对激子的束缚势是相当局域的。还观察到了激子在ZnSe_(0.92)Te_(0.08)阱层中的Te等电子陷阱能级与相邻(CdSe)_1/(ZnSe)_3短周期超晶格之间的转移现象。

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国家自然科学基金

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测量了ZnSe,Zn_(0.84)Mn_(0.16)Se合金和ZnSe/Zn_(0.84)Mn_(0.16)Se超晶格的10~300K的变温光致发光谱。发现ZnSe的带隙在10K时比Zn_(0.84)Mn_(0.16)Se合金的带隙小,而在300K时比合金的带隙大。预计ZnSe/Zn_(0.84)Mn_(0.16)Se超晶格中在130K附近会发生势阱层和势垒层的反转。在ZnSe/Zn_(0.84)Mn_(0.16)Se超晶格中观测到了这种反转但发生在80K附近。超晶格中Zn_(0.84)Mn_(0.16)Se层的应变可能是反转温度变低的原因。

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基于热力学平衡计算,首次给出以DMZn和H_2Se为源,MOVPE生长ZnSe的相图.文中讨论了ZnSe单一凝聚相区的范围,以及可能出ZnSe(s)+Zn(s)或ZnSe(s)+Se(1)两种双凝聚相区的条件.

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于2010-11-23批量导入

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于2010-11-23批量导入

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We show that part of the reflectance difference resonance near the E-0 energy of ZnSe is due to the anisotropic in-plane strain in the ZnSe thin films, as films grown on three distinctly different substrates, GaAs, GaP, and ZnS, all show the resonance at the same energy. Such anisotropic strain induced resonance is predicted and also observed near the E-1/E-1+Delta(1) energies in ZnSe grown on GaAs. The theory also predicts that there should be no resonance due to strain at, the E-0+Delta(0) energy, which is consistent with experiments. The strain anisotropy is rather independent of the ZnSe layer thickness, or whether the film is strain relaxed. For ZnSe films with large lattice mismatch with substrates, the resonance at the E-1/E-1+Delta(1) energies is absent, very likely due to the poor crystalline quality of the 20 nm or so surface layer. (C) 2000 American Vacuum Society. [S0734-211X(00)05604-3].

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Photocurrent (PC) spectra of ZnCdSe-ZnSe double multi-quantum wells are measured at different temperature. Its corresponding photocurrent derivative (PCD) spectra are obtained by computing, and the PCD spectra have greatly enhanced the sensitivity of the relative weak PC signals. The polarization dependence of the PC spectra shows that the transitions observed in the PC spectra are heavy-hole related, and the transition energy coincide well with the results obtained by envelope function approximation including strain. The temperature dependence of the photocurrent curves indicates that the thermal activation is the dominant transport mechanism of the carriers in our samples. The concept of saturation temperature region is introduced to explain why the PC spectra have different temperature dependence in the samples with different structure parameters. It is found to be very useful in designing photovoltaic devices.

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Novel 3D wurtzite ZnSe hierarchical nanostructures have been synthesized by a mild hydrothermal treatment. The as-prepared flowerlike nanostructures efficiently catalyze the photodegradation of methylene blue and ethyl violet present in aqueous solutions under UV light irradiation, exhibiting higher photocatalytic activity than the commercially available photocatalysts P25 and ZnSe microspheres. We also demonstrate that flowerlike morphology is important for the excellent photocatalytic activity.