可见和近红外区矿物的电子光谱

G. Rossman, B. Ehlmann
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引用次数: 6

摘要

矿物的许多光谱特征在可见到近红外区域(VNIR;这里定义为~ 0.4-2.5 μm),由过渡元素内部和之间的电子跃迁以及与它们化学结合的阴离子引起。数以千计的矿物在这部分光谱中具有颜色或波长可变的特性。金属离子包括钒、铬、锰、铁、钴、镍和铜,通常处于2+或3+氧化态,是许多矿物颜色的原因。然而,这些元素中只有少数,典型的是铁、钛和氧,在大多数岩石体遥感应用中是重要的。许多特征是由金属离子d轨道之间的电子跃迁产生的,而一些光谱特征是由原子之间的相互作用产生的。
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Electronic Spectra of Minerals in the Visible and Near-Infrared Regions
Many of the spectral features ofminerals in the visible to near-infrared region (VNIR; defined here as ~0.4–2.5 μm) arise from electronic transitions within and between transition elements and the anions chemically bound to them. Thousands of minerals have color or wavelengthvariable properties in this portion of the spectrum.Metal ions including vanadium, chromium, manganese, iron, cobalt, nickel, and copper, usually in either the 2+ or 3+ oxidation state, are responsible for the color of many minerals. However, only a few of these elements, typically iron, titanium, and oxygen, are important in most remote sensing applications of rocky bodies. Many features arise from electronic transitions of electrons between the d orbitals of a metal ion, while some spectroscopic features arise from interactions between atoms.
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