Institute of Physics, University Duisburg-Essen, Duisburg, Germany.
J Phys Condens Matter. 2010 Feb 3;22(4):045401. doi: 10.1088/0953-8984/22/4/045401. Epub 2010 Jan 5.
The discrepancy between Raman spectra of boron carbide obtained by Fourier transform Raman and conventional Raman spectrometry is systematically investigated. While at photon energies below the exciton energy (1.560 eV), Raman scattering of bulk phonons of boron carbide occurs, photon energies exceeding the fundamental absorption edge (2.09 eV) evoke additional patterns, which may essentially be attributed to luminescence or to the excitation of Raman-active processes in the surface region. The reason for this is the very high fundamental absorption in boron carbide inducing a very small penetration depth of the exciting laser radiation. Raman excitations essentially restricted to the boron carbide surface region yield spectra which considerably differ from bulk phonon ones, thus indicating structural modifications.
系统研究了傅里叶变换拉曼和常规拉曼光谱法获得的碳化硼的喇曼光谱之间的差异。当光子能量低于激子能量(1.560eV)时,发生碳化硼体声子的喇曼散射,而光子能量超过基本吸收边缘(2.09eV)时则会出现附加图案,这些图案可能主要归因于发光或表面区域中拉曼活性过程的激发。其原因是碳化硼的基本吸收非常高,导致激发激光辐射的穿透深度非常小。实质上仅限于碳化硼表面区域的喇曼激发产生的光谱与体声子光谱有很大的不同,从而表明结构发生了变化。