TY - JOUR
T1 - A recyclable biomass electrolyte towards green zinc-ion batteries
AU - Lu, Hongyu
AU - Hu, Jisong
AU - Wei, Xijun
AU - Zhang, Kaiqi
AU - Xiao, Xiao
AU - Zhao, Jingxin
AU - Hu, Qiang
AU - Yu, Jing
AU - Zhou, Guangmin
AU - Xu, Bingang
N1 - Funding Information:
G.Z. appreciates the support from the National Key Research and Development Program of China (2019YFA0705700), National Natural Science Foundation of China (U21A20174), Guangdong Innovative and Entrepreneurial Research Team Program (2021ZT09L197), Shenzhen Science and Technology Program (KQTD20210811090112002), the Start-up Funds, Interdisciplinary Research and Innovation Fund of Tsinghua Shenzhen International Graduate School, and the Tsinghua Shenzhen International Graduate School-Shenzhen Pengrui Young Faculty Program of Shenzhen Pengrui Foundation (SZPR2023007). J.Z. acknowledges financial support from the Research Grants Council of Hong Kong (RGC Postdoctoral Fellowship Scheme, Grant No.: PDFS2122-5S03).
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - The operation of traditional aqueous-electrolyte zinc-ion batteries is adversely affected by the uncontrollable growth of zinc dendrites and the occurrence of side reactions. These problems can be avoided by the development of functional hydrogel electrolytes as replacements for aqueous electrolytes. However, the mechanism by which most hydrogel electrolytes inhibit the growth of zinc dendrites on a zinc anode has not been investigated in detail, and there is a lack of a large-scale recovery method for mainstream hydrogel electrolytes. In this paper, we describe the development of a recyclable and biodegradable hydrogel electrolyte based on natural biomaterials, namely chitosan and polyaspartic acid. The distinctive adsorptivity and inducibility of chitosan and polyaspartic acid in the hydrogel electrolyte triggers a double coupling network and an associated synergistic inhibition mechanism, thereby effectively inhibiting the side reactions on the zinc anode. In addition, this hydrogel electrolyte played a crucial role in an aqueous acid-based Zinc/MnO2 battery, by maintaining its interior two-electron redox reaction and inhibiting the formation of zinc dendrites. Furthermore, the sustainable biomass-based hydrogel electrolyte is biodegradable, and could be recovered from the Zinc/MnO2 battery for subsequent recycling.
AB - The operation of traditional aqueous-electrolyte zinc-ion batteries is adversely affected by the uncontrollable growth of zinc dendrites and the occurrence of side reactions. These problems can be avoided by the development of functional hydrogel electrolytes as replacements for aqueous electrolytes. However, the mechanism by which most hydrogel electrolytes inhibit the growth of zinc dendrites on a zinc anode has not been investigated in detail, and there is a lack of a large-scale recovery method for mainstream hydrogel electrolytes. In this paper, we describe the development of a recyclable and biodegradable hydrogel electrolyte based on natural biomaterials, namely chitosan and polyaspartic acid. The distinctive adsorptivity and inducibility of chitosan and polyaspartic acid in the hydrogel electrolyte triggers a double coupling network and an associated synergistic inhibition mechanism, thereby effectively inhibiting the side reactions on the zinc anode. In addition, this hydrogel electrolyte played a crucial role in an aqueous acid-based Zinc/MnO2 battery, by maintaining its interior two-electron redox reaction and inhibiting the formation of zinc dendrites. Furthermore, the sustainable biomass-based hydrogel electrolyte is biodegradable, and could be recovered from the Zinc/MnO2 battery for subsequent recycling.
UR - http://www.scopus.com/inward/record.url?scp=85165384853&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-40178-0
DO - 10.1038/s41467-023-40178-0
M3 - Journal article
C2 - 37481665
AN - SCOPUS:85165384853
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 4435
ER -