Sensitive detection of surface- and size-dependent direct and indirect band gap transitions in ferritin

被引:19
作者
Colton, J. S. [1 ]
Erickson, S. D. [1 ]
Smith, T. J. [2 ]
Watt, R. K. [2 ]
机构
[1] Brigham Young Univ, Dept Phys & Astron, Provo, UT 84602 USA
[2] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
关键词
absorption spectroscopy; nanoparticles; band gaps; INFRARED-ABSORPTION; MAMMALIAN FERRITIN; REDOX REACTIONS; IRON; REACTIVITY; CORE; PHOTOREDUCTION; ENERGY; MODEL;
D O I
10.1088/0957-4484/25/13/135703
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ferritin is a protein nano-cage that encapsulates minerals inside an 8 nm cavity. Previous band gap measurements on the native mineral, ferrihydrite, have reported gaps as low as 1.0 eV and as high as 2.5-3.5 eV. To resolve this discrepancy we have used optical absorption spectroscopy, a well-established technique for measuring both direct and indirect band gaps. Our studies included controls on the protein nano-cage, ferritin with the native ferrihydrite mineral, and ferritin with reconstituted ferrihydrite cores of different sizes. We report measurements of an indirect band gap for native ferritin of 2.140 +/- 0.015 eV (579.7 nm), with a direct transition appearing at 3.053 +/- 0.005 eV (406.1 nm). We also see evidence of a defect-related state having a binding energy of 0.220 +/- 0.010 eV. Reconstituted ferrihydrite minerals of different sizes were also studied and showed band gap energies which increased with decreasing size due to quantum confinement effects. Molecules that interact with the surface of the mineral core also demonstrated a small influence following trends in ligand field theory, altering the native mineral's band gap up to 0.035 eV.
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页数:7
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