Lahiri Abhishek, Olschewski Mark, Gustus René, Borisenko Natalia, Endres Frank
Institute of Electrochemistry, Clausthal University of Technology, Arnold-Sommerfeld-Str. 6, 38678, Clausthal-Zellerfeld, Germany.
Phys Chem Chem Phys. 2016 Jun 1;18(22):14782-6. doi: 10.1039/c6cp02364a.
Sodium-ion batteries (SIBs) are emerging as potential stationary energy storage devices due to the abundance and low cost of sodium. A simple and energy efficient strategy to develop electrodes for SIBs with a high charge/discharge rate is highly desirable. Here we demonstrate that by surface modification of Ge, using electroless deposition in SbCl3/ionic liquids, the stability and performance of the anode can be improved. This is due to the formation of GexSb1-x at the surface leading to better diffusion of Na, and the formation of a stable twin organic and inorganic SEI which protects the electrode. By judicious control of the surface modification, an improvement in the capacity to between 50% and 300% has been achieved at high current densities (0.83-8.4 A g(-1)) in an ionic liquid electrolyte NaFSI-[Py1,4]FSI. The results clearly demonstrate that an electroless deposition based surface modification strategy in ionic liquids offers exciting opportunities in developing superior energy storage devices.
由于钠的储量丰富且成本低廉,钠离子电池(SIBs)正成为潜在的固定式储能装置。开发具有高充放电速率的SIBs电极需要一种简单且节能的策略。在此,我们证明通过在SbCl3/离子液体中进行化学镀对锗进行表面改性,可以提高阳极的稳定性和性能。这是由于在表面形成了GexSb1-x,从而使Na的扩散更好,并且形成了稳定的有机-无机孪晶固态电解质界面(SEI),保护了电极。通过对表面改性的明智控制,在离子液体电解质NaFSI-[Py1,4]FSI中,在高电流密度(0.83-8.4 A g(-1))下,容量提高了50%至300%。结果清楚地表明,基于化学镀的离子液体表面改性策略在开发优质储能装置方面提供了令人兴奋的机会。