TY - JOUR
T1 - Inherent Water Competition Effect-Enabled Colloidal Electrode for Ultra-stable Aqueous Zn-I Batteries
AU - Zhang, Kaiqiang
AU - Wu, Chao
AU - Yan, Shiye
AU - Ma, Changlong
AU - Wang, Luoya
AU - Kong, Pei
AU - Zhuang, Kun
AU - Fan, Pengcheng
AU - Ye, Jilei
AU - Wu, Yuping
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/10/30
Y1 - 2024/10/30
N2 - Electrode material stability is crucial for the development of next-generation ultralong-lifetime batteries. However, current solid- and liquid-state electrode materials face challenges such as rigid atomic structure collapse and uncontrolled species migration, respectively, which contradict the theoretical requirements for ultralong operation lifetimes. Herein, we present a design concept for a soft colloid polyvinylpyrrolidone iodine (PVP-I) electrode, leveraging the inherent water molecule competition effect between (SO4)2- from the electrolyte and PVP-I from the cathode in an aqueous Zn||PVP-I battery. Electrochemical demonstrations measured under various simulated and practical (integrated with photovoltaic solar panel) conditions highlight the potential for an ultralong battery lifetime. The PVP-I colloid exhibits a dynamic response to the electric field during battery operation. More importantly, the water competition effect between (SO4)2- from the electrolyte and water-soluble polymer cathode materials establishes a new electrolyte/cathode interfacial design platform for advancing ultralong-lifetime aqueous batteries.
AB - Electrode material stability is crucial for the development of next-generation ultralong-lifetime batteries. However, current solid- and liquid-state electrode materials face challenges such as rigid atomic structure collapse and uncontrolled species migration, respectively, which contradict the theoretical requirements for ultralong operation lifetimes. Herein, we present a design concept for a soft colloid polyvinylpyrrolidone iodine (PVP-I) electrode, leveraging the inherent water molecule competition effect between (SO4)2- from the electrolyte and PVP-I from the cathode in an aqueous Zn||PVP-I battery. Electrochemical demonstrations measured under various simulated and practical (integrated with photovoltaic solar panel) conditions highlight the potential for an ultralong battery lifetime. The PVP-I colloid exhibits a dynamic response to the electric field during battery operation. More importantly, the water competition effect between (SO4)2- from the electrolyte and water-soluble polymer cathode materials establishes a new electrolyte/cathode interfacial design platform for advancing ultralong-lifetime aqueous batteries.
UR - http://www.scopus.com/inward/record.url?scp=85208204266&partnerID=8YFLogxK
U2 - 10.1021/jacs.4c09352
DO - 10.1021/jacs.4c09352
M3 - 文章
C2 - 39421906
AN - SCOPUS:85208204266
SN - 0002-7863
VL - 146
SP - 29513
EP - 29522
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 43
ER -