Xie Weili, Zhu Kaiyue, Jiang Weikang, Yang Hanmiao, Ma Manxia, Zhao Lingli, Yang Weishen
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Dalian 116023 (China).
University of Chinese Academy of Sciences, Beijing 100049 (China).
ACS Nano. 2024 Aug 13;18(32):21184-21197. doi: 10.1021/acsnano.4c04181. Epub 2024 Aug 2.
Rechargeable aqueous zinc-ion batteries (AZIBs) are gaining recognition as promising next-generation energy storage solution, due to their intrinsic safety and low cost. Nevertheless, the advancement of AZIBs is greatly limited by the abnormal growth of zinc dendrites during cycling. Electrolyte additives are effective at suppressing zinc dendrites, but there is currently no effective additive screening criterion. Herein, we propose employing the interfacial electrostatic adsorption strength of zinc ions for the initial screening of additives. Subsequently, dendrite-free plating is achieved by employing the anionic surfactant sodium dodecyl benzenesulfonate (SDBS) to enhance electrostatic adsorption. The cycled zinc anode exhibited a dense plating morphology and a high (002) orientation (/ = 22). The Zn||MnO full cell with SDBS exhibited a capacity retention of 85% after 1000 cycles at 1 A g. Furthermore, an instantaneous nucleation model and continuous nucleation model (CNM) are constructed to reveal the microscale plating/stripping dynamics under the scenarios of weak adsorption and strong adsorption. The CNM accurately explains the self-optimizing reconstruction of electrodes resulting from enhanced electrostatic adsorption. Our exploration was extended to other anionic surfactants (sodium dodecyl sulfate and disodium laureiminodipropionate), confirming the effectiveness of strong electrostatic adsorption in the screening of electrolyte additives.
可充电水系锌离子电池(AZIBs)因其本质安全性和低成本,正作为一种有前景的下一代储能解决方案而受到认可。然而,AZIBs的发展受到循环过程中锌枝晶异常生长的极大限制。电解质添加剂在抑制锌枝晶方面是有效的,但目前尚无有效的添加剂筛选标准。在此,我们提出利用锌离子的界面静电吸附强度对添加剂进行初步筛选。随后,通过使用阴离子表面活性剂十二烷基苯磺酸钠(SDBS)增强静电吸附,实现了无枝晶电镀。循环后的锌阳极呈现出致密的电镀形态和较高的(002)取向(/ = 22)。含SDBS的Zn||MnO全电池在1 A g下循环1000次后容量保持率为85%。此外,构建了瞬时成核模型和连续成核模型(CNM),以揭示弱吸附和强吸附情况下微观尺度的电镀/剥离动力学。CNM准确解释了由增强静电吸附导致的电极自优化重构。我们的探索扩展到了其他阴离子表面活性剂(十二烷基硫酸钠和月桂酰亚氨基二丙酸钠),证实了强静电吸附在电解质添加剂筛选中的有效性。