Sibo Wang, Wanlong Wu, Quanwei Jiang, Chen Li, Hua-Yu Shi, Xiao-Xia Liu and Xiaoqi Sun
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引用次数: 0
Abstract
Aqueous Zn–S batteries provide competitive energy density for large-scale energy storage systems. However, the cathode active material exhibits poor electrical conductivity especially at the discharged state of ZnS. Its morphology generated in cells thus directly determines the cathode electrochemical activity. Here, we reveal the ZnS growth behavior and control its morphology by the anion donor number (DN) of zinc salts in electrolytes. The anion DN affects the salt dissociation degree and furthermore sulfide solubility in electrolytes, which finally determines ZnS growth preference on existing nuclei or carbon substrates. As a result, 3D ZnS is realized from the high DN ZnBr2 electrolyte, whereas a 2D passivation film is formed from low DN Zn(TFSI)2. Thanks to the facile electron paths and abundant reaction sites with 3D morphology, the sulfur cathode reaches a high capacity of 1662 mA h g−1 at 0.1 A g−1 and retains 872 mA h g−1 capacity after 400 cycles at 3 A g−1.
含水锌-s电池为大规模储能系统提供具有竞争力的能量密度。然而,阴极活性材料表现出较差的导电性,特别是在ZnS放电状态下。它在电池中产生的形态直接决定了阴极的电化学活性。本研究揭示了电解质中锌盐阴离子给体数(DN)对ZnS生长行为和形貌的控制。阴离子DN影响盐解离度,进而影响硫化物在电解质中的溶解度,最终决定了ZnS在现有核或碳底物上的生长偏好。结果表明,高DN ZnBr2电解质可实现三维ZnS,而低DN Zn(TFSI)2可形成二维钝化膜。在0.1 a g−1条件下,硫阴极的电容量可达1662 mA h g−1,在3 a g−1条件下循环400次后,其电容量仍可达872 mA h g−1。
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.