2017
DOI: 10.1016/j.mssp.2017.02.026
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Solubility, diffusion and electrical activity of Na in bulk Ge crystals

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Cited by 10 publications
(19 citation statements)
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“…Owing to their ability to form an amorphous layer and high‐density dislocations near the propagating interface (see Figures 7c,d), alloying anodes following DCR diffusion enable the faster diffusion of carrier ions into the anodes. When the diffusivities of alloying anodes are compared, the diffusivities (≈3.0 × 10 −6 cm 2 s −1 for Na–Sn [ 82 ] and ≈3.6 × 10 −7 cm 2 s −1 for Na–Ge [ 112 ] ) of carrier ions in DCR‐governed alloying anodes are greater than those (≈5.1 × 10 −12 cm 2 s −1 for Li–Si [ 113 ] and ≈3.0 × 10 −10 cm 2 s −1 for Na–Sb [ 114 ] ) of ICR‐governed alloying anodes by more than three to five orders of magnitude. Therefore, the selection of the DCR‐governed alloying anodes can prevent the depletion of charge carriers at high current rates, making them suitable for high‐power operations.…”
Section: Discussionmentioning
confidence: 99%
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“…Owing to their ability to form an amorphous layer and high‐density dislocations near the propagating interface (see Figures 7c,d), alloying anodes following DCR diffusion enable the faster diffusion of carrier ions into the anodes. When the diffusivities of alloying anodes are compared, the diffusivities (≈3.0 × 10 −6 cm 2 s −1 for Na–Sn [ 82 ] and ≈3.6 × 10 −7 cm 2 s −1 for Na–Ge [ 112 ] ) of carrier ions in DCR‐governed alloying anodes are greater than those (≈5.1 × 10 −12 cm 2 s −1 for Li–Si [ 113 ] and ≈3.0 × 10 −10 cm 2 s −1 for Na–Sb [ 114 ] ) of ICR‐governed alloying anodes by more than three to five orders of magnitude. Therefore, the selection of the DCR‐governed alloying anodes can prevent the depletion of charge carriers at high current rates, making them suitable for high‐power operations.…”
Section: Discussionmentioning
confidence: 99%
“…This is especially true when the diffusivity of the carrier ions is lower in the SEIs than in the anodes. [ 118,119 ] For instance, the carrier‐ion diffusivity (≈1.8 × 10 −13 to 7.6 × 10 −11 cm 2 s −1[ 120 ] ) in SEIs is much lower than the typical values (e.g., ≈3.0 × 10 −6 cm 2 s −1 for Na–Sn [ 82 ] and ≈3.6 × 10 −7 cm 2 s −1 for Na–Ge [ 112 ] ) in DCR‐governed alloying anodes. In this case, the overall diffusion rate is limited by the SEI, rather than by the propagating interface or the trailing bulk region.…”
Section: Discussionmentioning
confidence: 99%
“…The donor impurity that is most often used and provides the necessary optical properties of Ge crystals is antimony, atoms of which substitute Ge atoms in the crystal lattice. However, we have managed to dope Ge crystals with an interstitial Na and to show that the optical parameters of single-crystalline and coarsegrained Ge:Na are better as compared with those of Ge:Sb grown from the same raw material [5,6].…”
Section: Related Workmentioning
confidence: 99%
“…As it was shown by us previously [5], among the advantages of Ge:Na crystals over Ge:Sb crystals there is a significantly lower scattering of transmitted radiation. This is due not only to the fact that introduction of smallsize interstitial Na atoms into germanium leads to less distortions of the crystal lattice as compared with substitutional impurity Sb in Ge, but also to lower solubility of Na in Ge (about 10 15 atoms/cm 3 ) [6] as compared with Sb. The maximum solubility of Sb in Ge crystals is 1.2·10 19 atoms/cm 3 [15], Sb has a retrograde solubility in Ge, and, as a result, while cooling the grown Ge:Sb crystals from the growth temperature to the room one, second-phase inclusions of Sb with characteristic sizes about 6…9 µm are formed, and they scatter the infrared radiation [16].…”
Section: Nomentioning
confidence: 99%
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