TY - JOUR
T1 - Amorphization driven Na-alloying in SixGe1−xalloy nanowires for Na-ion batteries
AU - Abdul Ahad, Syed
AU - Kilian, Seamus
AU - Zubair, Maria
AU - Lebedev, Vasily A.
AU - McNamara, Karrina
AU - Ryan, Kevin M.
AU - Kennedy, Tadhg
AU - Geaney, Hugh
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2021.
PY - 2021/9/28
Y1 - 2021/9/28
N2 - Here we report the use of 1D SixGe1−x(x= 0.25, 0.5, 0.75) alloy nanowires (NWs) as anode materials for Na-ion batteries (NIBs). The strategy involves the synthesis of crystalline SixGe1−xNWsviathe solution-liquid-solid (SLS) mechanism, followed by amorphization to activate the material for Na-ion cycling within a NIB. This study demonstrates the successful activation of SixGe1−xamorphous NW alloys, with a-Si0.5Ge0.5delivering 250 mA h g−1as compared to a-Ge NWs delivering only 107 mA h g−1after 100 cycles. Also, amorphization proved to be a critical step, since crystalline NWs failed to activate in NIBs. However, Si NWs performed poorly during Na-ion cycling even after amorphization, and this behavior was explained by poor comparative Na-ion diffusivity. Further investigations on the impact of the relative content of Ge within the amorphized SixGe1−xNWs, Na-ion diffusivity and electrode degradation during cycling were also performed. Notably, the incorporation of Ge in the a-SixGe1−xalloy boosted Na ion diffusivity in the amorphized alloy, resulting in improved cycling performance and rate capability as compared to parent a-Si and a-Ge NWs.
AB - Here we report the use of 1D SixGe1−x(x= 0.25, 0.5, 0.75) alloy nanowires (NWs) as anode materials for Na-ion batteries (NIBs). The strategy involves the synthesis of crystalline SixGe1−xNWsviathe solution-liquid-solid (SLS) mechanism, followed by amorphization to activate the material for Na-ion cycling within a NIB. This study demonstrates the successful activation of SixGe1−xamorphous NW alloys, with a-Si0.5Ge0.5delivering 250 mA h g−1as compared to a-Ge NWs delivering only 107 mA h g−1after 100 cycles. Also, amorphization proved to be a critical step, since crystalline NWs failed to activate in NIBs. However, Si NWs performed poorly during Na-ion cycling even after amorphization, and this behavior was explained by poor comparative Na-ion diffusivity. Further investigations on the impact of the relative content of Ge within the amorphized SixGe1−xNWs, Na-ion diffusivity and electrode degradation during cycling were also performed. Notably, the incorporation of Ge in the a-SixGe1−xalloy boosted Na ion diffusivity in the amorphized alloy, resulting in improved cycling performance and rate capability as compared to parent a-Si and a-Ge NWs.
UR - http://www.scopus.com/inward/record.url?scp=85115693312&partnerID=8YFLogxK
U2 - 10.1039/d1ta03741b
DO - 10.1039/d1ta03741b
M3 - Article
AN - SCOPUS:85115693312
SN - 2050-7488
VL - 9
SP - 20626
EP - 20634
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 36
ER -