Key Laboratory of Polar Materials and Devices, Ministry of Education, Department of Electronic Engineering, East China Normal University, Shanghai 200241, People's Republic of China.
Phys Chem Chem Phys. 2011 Jul 28;13(28):13096-105. doi: 10.1039/c0cp02924f. Epub 2011 Jun 21.
Iron (Fe)-doped (0 to 4%) TiO(2) nano-crystalline (nc) films with the grain size of about 25 nm have been deposited on n-type Si (100) substrates by a facile nonhydrolytic sol-gel processing. X-ray diffraction measurements prove that the films are polycrystalline and present the pure anatase phase. X-ray photoelectron spectroscopy spectra indicate that the chemical valent state of Fe element is +3 and the Fe(3+) ions replace the Ti(4+) sites. The Fe dopant effects on the surface morphology, microstructure, and dielectric functions of the nc-Fe/TiO(2) films have been studied by atomic force microscope, ultraviolet Raman scattering and spectroscopic ellipsometry. With increasing Fe composition, the intensity of Raman-active mode B(1g) increases, while that of the A(1g) phonon mode decreases. The dielectric functions have been uniquely extracted by fitting ellipsometric spectra with the Adachi's dielectric function model and a four-phase layered model. It is found that the real part of dielectric functions in the transparent region and the optical band gap slightly decrease with the Fe composition due to the introduction of acceptor level Fe t(2g). Finally, the composition and temperature dependence of the surface and lattice defects in the Fe/TiO(2) films have been investigated by photoluminescence spectra in detail. At room temperature, the emission intensities decrease with increasing Fe compositions since the Fe incorporation could prolong the radiative lifetime and/or shorten the non-radiative lifetime. By analyzing the low temperature photoluminescence spectra, the intensities and positions of five emission peaks and shoulder structure can be unambiguously assigned. The phenomena could be reasonably explained by the physical mechanisms such as oxygen vacancies, localized excitons, self-trapped excitons, and indirect transitions, which are strongly related to the electronic band structure perturbed by the Fe doping.
铁(Fe)掺杂(0 至 4%)的 TiO2 纳米晶(nc)薄膜具有约 25nm 的晶粒尺寸,通过简便的非水解溶胶-凝胶工艺沉积在 n 型 Si(100)衬底上。X 射线衍射测量证明了这些薄膜是多晶的,呈现出纯锐钛矿相。X 射线光电子能谱表明,Fe 元素的化学价态为+3,Fe(3+)离子取代 Ti(4+)位。原子力显微镜、紫外拉曼散射和光谱椭圆偏振术研究了 Fe 掺杂对 nc-Fe/TiO2 薄膜表面形貌、微观结构和介电函数的影响。随着 Fe 成分的增加,拉曼活性模式 B(1g)的强度增加,而 A(1g)声子模式的强度减小。通过用 Adachi 介电函数模型和四相分层模型拟合椭圆偏振光谱,独特地提取了介电函数。发现由于受主能级 Fe t(2g)的引入,透明区介电函数的实部和光学带隙略微减小。最后,详细研究了 Fe/TiO2 薄膜的表面和晶格缺陷的组成和温度依赖性。在室温下,随着 Fe 成分的增加,发射强度减小,因为 Fe 的掺入可以延长辐射寿命和/或缩短非辐射寿命。通过分析低温光致发光光谱,可以明确地分配五个发射峰和肩峰结构的强度和位置。这些现象可以通过物理机制(如氧空位、局域激子、自陷激子和间接跃迁)得到合理的解释,这些机制与 Fe 掺杂引起的电子能带结构的扰动密切相关。