Lithium Growth on Alloying Substrates and Effect on Volumetric Expansion

The widespread implementation of next-generation Li metal anodes is limited, in part, due to the formation of dendritic and/or mossy electrodeposits during cycling. These morphologies can lead to battery failure due to the formation of short circuits and significant volumetric expansion at the anode. One strategy to control the electrodeposition of Li metal is to use lithiophilic materials at the anode. Here, we evaluate the impact of Ag and Au on the early stages of Li metal electrodeposition and cycling. The alloying substrates decrease the voltage for Li reduction and improve Li wetting/adhesion. We probe volumetric expansion directly through dilatometry measurements and find that the degree of volumetric expansion is less when lithium is cycled on an alloying substrate compared to a non-alloying substrate (Cu). Dilatometry experiments reveal that Au has the least amount of volumetric expansion and coin cell cycling experiments indicate that Ag yields more stable cycling compared to Au or Cu. The evaluation of in situ cross-sectional images of cycled coin cells shows that Ag has the lowest volumetric expansion in a coin cell format.. Authors: Merrill, Laura Christine [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)] (ORCID:0000000176734519); Craig, Robert Lee [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)]; Cummings, Damion P. [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)]; Deitz, Julia Irene [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)] (ORCID:0000000251543027). DOE Contract: NA0003525. Subjects: alloys; batteries; dilatometry; laser plasma focused ion beam; lithiophilic; lithium anodes; volumetric expansion