TY - JOUR
T1 - Cr2O3-x artificial interfacial layer featuring abundant nucleation sites
T2 - Facilitating rapid Zn2+ transport and highly reversible Zn anode
AU - Nie, Zixiao
AU - Wang, Long
AU - Li, Jialei
AU - Li, Zhuo
AU - Xu, Hao
AU - Cheng, Yonghong
AU - Chen, Yu
AU - Xiao, Bing
AU - Xu, Xin
N1 - Publisher Copyright:
© 2025 Elsevier Inc.
PY - 2025/11
Y1 - 2025/11
N2 - Interfacial engineering offers a promising solution to zinc anode instability, yet most studies focus solely on suppressing side reactions with water, overlooking the critical role of fast zinc ion kinetics. This work investigates the Cr2O3-x artificial interface layer, demonstrating its dual benefits of electrostatic shielding and enhanced Zn2+ transport kinetics. The Cr2O3-x layer exhibits excellent mechanical stability and hydrophilicity, with its negatively charged surface effectively repelling anions like SO42− and OH− to suppress side reactions. Moreover, the highly active Cr2O3-x layer accelerates Zn2+ migration, reduces nucleation energy barriers, and promotes uniform zinc deposition by facilitating Zn2+ detachment from solvated structures. As a result, the Cr2O3-x@Zn anode achieves exceptional cycling stability and remarkable reversibility, with symmetric batteries enduring over 1,800 h at 5 mA cm−2. When paired with NH4V4O10, it also demonstrates long cycle life and superior rate performance. This work sheds new light on the development of stable, high-performance zinc anodes.
AB - Interfacial engineering offers a promising solution to zinc anode instability, yet most studies focus solely on suppressing side reactions with water, overlooking the critical role of fast zinc ion kinetics. This work investigates the Cr2O3-x artificial interface layer, demonstrating its dual benefits of electrostatic shielding and enhanced Zn2+ transport kinetics. The Cr2O3-x layer exhibits excellent mechanical stability and hydrophilicity, with its negatively charged surface effectively repelling anions like SO42− and OH− to suppress side reactions. Moreover, the highly active Cr2O3-x layer accelerates Zn2+ migration, reduces nucleation energy barriers, and promotes uniform zinc deposition by facilitating Zn2+ detachment from solvated structures. As a result, the Cr2O3-x@Zn anode achieves exceptional cycling stability and remarkable reversibility, with symmetric batteries enduring over 1,800 h at 5 mA cm−2. When paired with NH4V4O10, it also demonstrates long cycle life and superior rate performance. This work sheds new light on the development of stable, high-performance zinc anodes.
KW - CrO@Zn anode
KW - Electrostatic shielding
KW - Interfacial engineering
KW - Solvated structures
KW - Zn transport kinetics
UR - https://www.scopus.com/pages/publications/105005508502
U2 - 10.1016/j.jcis.2025.137918
DO - 10.1016/j.jcis.2025.137918
M3 - 文章
C2 - 40403527
AN - SCOPUS:105005508502
SN - 0021-9797
VL - 697
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
M1 - 137918
ER -