2D Silicon–Germanium-Layered Materials as Anodes for Li-Ion Batteries
Source abstract
Abstract
To address the volume changes of Si-based and Ge-based anode materials during lithiation and delithiation, two-dimensional (2D) composites like siloxene and germanane have recently been developed. These 2D materials can insert alkali cations without an alloying reaction, thereby limiting the associated volume expansion. While Si has a high theoretical capacity and low cost, its electrical conductivity is low; on the other hand, Ge provides a higher electronic conductivity but at a higher cost. Therefore, we propose a series of 2D Si–Ge alloys, that is, Si1–xGex with 0.1 < x < 0.9, referred to as siliganes, with reasonable cost and encouraging electrochemical performance. The layered siliganes were obtained by fully deintercalating Ca cations from the Ca(Si1–xGex)2 parent phases and used as Li-ion battery (LIB) anodes. XRD, SEM, Raman spectroscopy, and infrared spectroscopy were used to characterize the materials and identify the mechanisms occurring during cycling in LIBs. Siligane_Si0.9Ge0.1 was identified as the best candidate; at a current density of 0.05 A g–1, after 10 cycles, it showed a reversible capacity of 1325 mA h g–1, with high capacity retention and coulombic efficiency.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · MXene and MAX Phase Materials · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Université de Picardie Jules Verne Laboratoire de Réactivité et Chimie des Solides (LRCS), 15 Rue Baudelocque, Amiens 80000, France
Réseau sur le Stockage Electrochimique de l’Energie (RS2E), 15 Rue Baudelocque, 80000 Amiens, France
ALISTORE European Research Institute, 15 Rue Baudelocque, Amiens 80000, France
Department of Physics, Chalmers University of Technology, Chalmersplatsen 4, Göteborg 412 96, Sweden
Funding
Labex
References (28)
Show source-provided references
1. 10.1002/aenm.20130088210.1002/aenm.201300882 ↗
2. 10.1038/s41467-019-10305-x10.1038/s41467-019-10305-x ↗
3. 10.1016/j.pmatsci.2014.02.00110.1016/j.pmatsci.2014.02.001 ↗
4. 10.1021/nl403979s10.1021/nl403979s ↗
5. 10.1039/c6ta09831b10.1039/c6ta09831b ↗
6. 10.1002/aenm.20160002510.1002/aenm.201600025 ↗
7. 10.1016/j.jpowsour.2019.02.03010.1016/j.jpowsour.2019.02.030 ↗
8. 10.1002/batt.20190019810.1002/batt.201900198 ↗
9. 10.1002/adma.20180083810.1002/adma.201800838 ↗
10. 10.1021/acsami.8b1532310.1021/acsami.8b15323 ↗
11. 10.1021/acsenergylett.1c0028510.1021/acsenergylett.1c00285 ↗
12. 10.1016/j.physb.2011.07.05210.1016/j.physb.2011.07.052 ↗
13. 10.1088/2053-1591/2/1/01630110.1088/2053-1591/2/1/016301 ↗
14. 10.1016/j.commatsci.2019.04.03910.1016/j.commatsci.2019.04.039 ↗
15. 10.1016/s0022-0248(01)00686-810.1016/s0022-0248(01)00686-8 ↗
16. 10.1515/znb-1980-010810.1515/znb-1980-0108 ↗
17. 10.1016/j.jssc.2007.03.00310.1016/j.jssc.2007.03.003 ↗
18. 10.1016/j.jssc.2014.10.03310.1016/j.jssc.2014.10.033 ↗
19. 10.1002/anie.20060032110.1002/anie.200600321 ↗
20. 10.1103/physrevb.62.1139210.1103/physrevb.62.11392 ↗
21. 10.1016/j.actamat.2018.03.06310.1016/j.actamat.2018.03.063 ↗
22. 10.1021/acs.chemmater.7b0499010.1021/acs.chemmater.7b04990 ↗
23. 10.1103/physreva.43.316110.1103/physreva.43.3161 ↗
24. 10.1016/j.jpowsour.2004.07.03210.1016/j.jpowsour.2004.07.032 ↗
25. 10.1149/2.0021510eel10.1149/2.0021510eel ↗
26. 10.1021/cm501233k10.1021/cm501233k ↗
27. 10.1021/acs.jpcc.7b1124910.1021/acs.jpcc.7b11249 ↗
28. 10.1039/c8ee00160j10.1039/c8ee00160j ↗