Cai Xiaomin, Tian Wenzhi, Zhang Zekai, Sun Yan, Yang Lei, Mu Hongchun, Lian Cheng, Qiu Huibin
School of Chemistry and Chemical Engineering, Zhangjiang Institute for Advanced Study, Frontiers Science Center for Transformative Molecules, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai, 200240, P. R. China.
State Key Laboratory of Chemical Engineering, Shanghai Engineering Research Center of Hierarchical Nanomaterials, Frontiers Science Center for Materiobiology and Dynamic Chemistry, and School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Adv Mater. 2024 Jan;36(3):e2307727. doi: 10.1002/adma.202307727. Epub 2023 Nov 30.
Decorating Zn anodes with functionalized polymers is considered as an effective strategy to inhibit dendrite growth. However, this normally brings extra interfacial resistance rendering slow reaction kinetics of Zn . Herein, a poly(2-vinylpyridine) (P2VP) coating with modulated coordination strength and ion conductivity for dendrite-free Zn anode is reported. The P2VP coating favors a high electrolyte wettability and rapid Zn migration speed (Zn transfer number, t = 0.58). Electrostatic potential calculation shows that P2VP mildly coordinates with Zn (adsorption energy = -0.94 eV), which promotes a preferential deposition of Zn along the (002) crystal plane. Notably, the use of partially (26%) quaternized P2VP (q-P2VP) further reduces the interfacial resistance to 126 Ω, leading to a high ion migration speed (t = 0.78) and a considerably low nucleation overpotential (18 mV). As a result of the synergistic effect of mild coordination and partial electrolysis, the overpotential of the q-P2VP-decorated Zn anode retains at a considerably low level (≈46 mV) over 1000 h at a high current density of 10 mA cm . The assembled (NH ) V O ·1.5H O || glass fiber || q-P2VP-Zn full cell reveals a lower average capacity decay rate of only 0.018% per cycle within 500 cycles at 1 A g .
用功能化聚合物修饰锌阳极被认为是抑制枝晶生长的有效策略。然而,这通常会带来额外的界面电阻,导致锌的反应动力学缓慢。在此,报道了一种具有调制配位强度和离子电导率的聚(2-乙烯基吡啶)(P2VP)涂层,用于无枝晶锌阳极。P2VP涂层具有高电解质润湿性和快速的锌迁移速度(锌转移数,t = 0.58)。静电势计算表明,P2VP与锌轻度配位(吸附能 = -0.94 eV),这促进了锌沿(002)晶面的优先沉积。值得注意的是,使用部分(26%)季铵化的P2VP(q-P2VP)进一步将界面电阻降低至126 Ω,导致高离子迁移速度(t = 0.78)和相当低的成核过电位(18 mV)。由于轻度配位和部分电解的协同作用,在10 mA cm 的高电流密度下,q-P2VP修饰的锌阳极的过电位在1000 h内保持在相当低的水平(≈46 mV)。组装的(NH₄)₃VO₄·1.5H₂O||玻璃纤维||q-P2VP-Zn全电池在1 A g 的电流密度下500次循环内显示出仅0.018%/循环的较低平均容量衰减率。