Electrochemical assessment of highly reversible SnO2-coated Zn metal anodes prepared via atomic layer deposition for aqueous Zn-ion batteries
- Authors
- Gong, Sang Hyuk; Lim, Hyo Jin; Lee, Ji Hyeon; Yoo, Yiseul; Yu, Seungho; Lim, Hee-Dae; Jung, Hyun Wook; Ko, Jesse S.; Kim, In Soo; Kim, Hyung-Seok
- Issue Date
- Feb-2023
- Publisher
- ELSEVIER
- Keywords
- Aqueous zinc -ion battery; Zinc metal anode; Atomic layer deposition; Tin oxide
- Citation
- APPLIED SURFACE SCIENCE, v.611, pp.1 - 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- APPLIED SURFACE SCIENCE
- Volume
- 611
- Start Page
- 1
- End Page
- 10
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186249
- DOI
- 10.1016/j.apsusc.2022.155633
- ISSN
- 0169-4332
- Abstract
- Aqueous electrochemical energy storage systems that rely on earth-abundant elements are considered as cost-effective alternatives to current lithium-ion batteries which have dominated the technological landscape. For zinc-based energy storage, dendrite growth is an underlying challenge that needs to be addressed to enact high performance and long-term stability. In the present study, we employ atomic layer deposition to produce a thin tin oxide layer that allows dendrite-free cycling for aqueous zinc-ion batteries. Tin oxide is particularly inter-esting as it provides two distinct advantages-dendrite-free cycling and mitigation of parasitic hydrogen gas evolution. The presence of the tin oxide layer leads to hydrogen gas suppression and homogeneous zinc plating/ stripping, both of which are essential to improve the performance of zinc-ion batteries. When paired in a full-cell configuration with manganese oxide, this anode delivers a high specific capacity of 273 mAh g-1 at an imposed current rate of 100 mA g-1. Through density functional theory calculations, we elucidate further that the adsorption energy of Zn for bare Zn is higher than that in the presence of a tin oxide layer.
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