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首页> 外文期刊>The American mineralogist >Spinels Renaissance: The past, present, and future of those ubiquitous minerals and materials Color of Mn-bearing gahnite: A first example of electronic transitions in heterovalent exchange coupled IVMn~(2+)-VIMn~(3+) pairs in minerals?
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Spinels Renaissance: The past, present, and future of those ubiquitous minerals and materials Color of Mn-bearing gahnite: A first example of electronic transitions in heterovalent exchange coupled IVMn~(2+)-VIMn~(3+) pairs in minerals?

机译:尖晶石复兴:那些无处不在的矿物和材料的过去,现在和未来锰锰矿的颜色:矿物中IVMn〜(2 +)-VIMn〜(3+)对偶联的异价交换中电子跃迁的第一个例子?

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摘要

A natural yellow and transparent crystal of Mn-bearing, Mg-rich gahnite (ZnAl_2O4) from Nordmark (Sweden) was studied by electron microprobe, single-crystal X?ray diffraction and optical absorption spectroscopy. The empirical structural formula of the crystal, ~T(Zn_(0.52)Mg_(0.34)Mn_(0.08)~(2+)Al_(0.06))_(Σ1.00) ~M(Al_(1.88) Mn_(0.06)~(3+)Fe_(0.01)~(3+j)Mg_(0.04)Mn_(0.01)~(2+))_(Σ2.00 O4), shows that Mn~(2+) and Mn~(3+) are almost completely ordered at the T and M sites, respectively. The electronic absorption spectrum of the spinel shows, in addition to a strong UV-absorption edge (O~(2-)-Mn~(3+) and O~(2-)-Fe~(3+) ligand-metal charge transfers) and two broad ~(VI)Mn~(3+)-bands, a set of relatively narrow absorption bands at energies comparable to those caused by spin-forbidden electron transitions in tetrahedrally coordinated Mn~(2+) in oxide spinel. However, the set of bands in the present spectrum is shifted to lower energies and they are intensified by approximately an order of magnitude compared to those recorded for spin-forbidden IVMn~(2+)-bands in spinel. These characteristic differences in combination with the determined cation distribution in the present gahnite demonstrates that electronic transitions in exchange coupled ~(IV)Mn~(2+)-VIMn~(3+) pairs cause its color.
机译:通过电子探针,单晶X射线衍射和光学吸收光谱法研究了来自Nordmark(瑞典)的天然黄色且透明的含Mn,富Mg轻铁(ZnAl_2O4)晶体。晶体的经验结构式〜T(Zn_(0.52)Mg_(0.34)Mn_(0.08)〜(2+)Al_(0.06))_(Σ1.00)〜M(Al_(1.88)Mn_(0.06) 〜(3+)Fe_(0.01)〜(3 + j)Mg_(0.04)Mn_(0.01)〜(2 +))_(Σ2.00O4),表明Mn〜(2+)和Mn〜(3 +)几乎分别在T和M站点完全订购。尖晶石的电子吸收光谱显示出强的紫外线吸收边缘(O〜(2-)-Mn〜(3+)和O〜(2-)-Fe〜(3+)配体-金属电荷)和两个宽的〜(VI)Mn〜(3+)谱带,一组相对较窄的吸收带,其能量可与氧化物尖晶石中四面体配位的Mn〜(2+)的自旋禁止电子跃迁所引起的吸收谱带相比较。但是,与尖晶石中自旋禁止的IVMn〜(2+)谱带记录的谱带相比,本光谱中的谱带组转移到较低的能量,并且增强了大约一个数量级。这些特征差异与在本轻铁矿中确定的阳离子分布相结合,表明在交换耦合的〜(IV)Mn〜(2 +)-VIMn〜(3+)对中的电子跃迁引起其颜色。

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