Electrodepositing Textured Sn Film as a Highly Reversible Anode for Aqueous Batteries.

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Haozhe Zhang,Yanxia Yu,Diyu Xu,Minghao Zhang,Chen-Jui Huang,Jianxin Wang,Hao Liu,Fan Yang,Mingqian Li,Di-Jia Liu,Xihong Lu,Kang Xu,Ying Shirley Meng
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Abstract

Electrodepositing metal materials in large capacity, at low potential, and with high reversibility serves as the foundation for any aqueous rechargeable battery chemistry to realize the promises of high energy, low cost, and high safety. However, such a foundation is not solid because of the natural tendency of metals to form irregular, nonplanar, and often dendritic morphologies during electrochemical crystallization, which is further amplified in an acidic environment due to the faster kinetics of the coupled proton and mass-transport processes between hydrated metal ions and free metal atoms. As a typical representative, tin metal (Sn0) has potential to achieve high energy in acidic batteries, but its nonuniform large-particle morphology, obtained from traditional electrodeposition, leads to dead Sn0 formation and deteriorating reversibility, accompanied by the sustained hydrogen evolution reaction (HER) and active Sn0 loss. Here, we report quaternary onium salts as effective interfacial cocations that, via selective adsorption, steadily texturize Sn0 deposition along the (211) plane, which is intrinsically inert to the HER, thus regulating the film deposition process by favoring the formation of planar Sn0 film. Such Sn0 film brings exceptional reversibility in acidic electrolytes, which translates into sustained cycling stability at applicable areal capacities in both anode-half cells (∼1500 deposition/dissolution cycles at 5 mAh cm-2) and full cells (350 charge/discharge cycles at 5 mAh cm-2). Textured electrodeposition with intrinsic HER-suppression capability provides a universal solution for diverse metal anode materials in rechargeable energy-dense aqueous batteries.
电沉积织构锡膜作为水电池的高可逆阳极。
电沉积大容量、低电位、高可逆性的金属材料,是实现高能量、低成本、高安全的任何水性可充电电池化学的基础。然而,这样的基础并不牢固,因为金属在电化学结晶过程中自然倾向于形成不规则的、非平面的、经常是枝晶状的形态,在酸性环境中,由于水合金属离子和自由金属原子之间的耦合质子和质量传递过程的动力学更快,这进一步放大了。作为典型代表的锡金属(Sn0)在酸性电池中具有实现高能量的潜力,但由于传统电沉积方法所获得的大颗粒形态不均匀,导致了死Sn0的形成和可逆性的恶化,伴随着持续的析氢反应(HER)和活性Sn0的损失。在这里,我们报道了季铵盐作为有效的界面剂,通过选择性吸附,稳定地沿着(211)平面织构Sn0沉积,这对HER具有内在惰性,从而通过有利于平面Sn0膜的形成来调节薄膜沉积过程。这种Sn0薄膜在酸性电解质中具有优异的可逆性,在阳极半电池(5mah cm-2时沉积/溶解循环~ 1500次)和完整电池(5mah cm-2时充电/放电循环350次)的适用面积容量下,可转化为持续的循环稳定性。具有内在her抑制能力的织构电沉积为可充电高能量密度水电池中各种金属阳极材料提供了一种通用的解决方案。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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