Soft X-ray synchrotron radiation spectroscopy study of molecule-based nanoparticles

被引:0
|
作者
Lee, Eunsook [1 ]
Kim, D. H. [1 ]
Kang, J. -S. [1 ]
Kim, Kyung Hyun [2 ]
Kim, Pil [3 ]
Baik, Jaeyoon [4 ]
Shin, H. J. [4 ]
机构
[1] Catholic Univ Korea, Dept Phys, Puchon 420743, South Korea
[2] Korea Univ, Dept Biotechnol & Bioinformat, Jochiwon 339700, South Korea
[3] Catholic Univ Korea, Dept Biotechnol, Puchon 420743, South Korea
[4] POSTECH, Pohang Accelerator Lab, Pohang 790784, South Korea
基金
新加坡国家研究基金会;
关键词
XAS; Prussian blue analogue; Ferritin; Electronic structure; PES; PRUSSIAN BLUE ANALOGS; PHOTOINDUCED FERRIMAGNETIC SYSTEMS; TRANSITION-METAL COMPOUNDS; ALKALI CATION; C-I; ABSORPTION SPECTROSCOPY; ELECTRON-TRANSFER; CHARGE-TRANSFER; TEMPERATURE; FERRITIN;
D O I
10.3938/jkps.65.1551
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The electronic structures of molecule-based nanoparticles, such as biomineralized Helicobacter pylori ferritin (Hpf), Heme, and RbCo[Fe(CN)(6)]H2O (RbCoFe) Prussian blue analogue, have been investigated by employing photoemission spectroscopy and soft X-ray absorption spectroscopy. Fe ions are found to be nearly trivalent in Hpf and Heme nanoparticles, which provides evidence that the amount of magnetite (Fe3O4) should be negligible in the Hpf core and that the biomineralization of Fe oxides in the high-Fe-bound-state Hpf core arises from a hematite-like formation. On the other hand, Fe ions are nearly divalent and Co ions are Co2+-Co3+ mixed-valent in RbCoFe. Therefore this finding suggests that the mechanism of the photo-induced transition in RbCoFe Prussian blue analogue is not a simple spin-state transition of Fe2+-Co3+ -> Fe3+-Co2+. It is likely that Co2+ ions have the high-spin configuration while Fe2+ ions have the low-spin configuration.
引用
收藏
页码:1551 / 1554
页数:4
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