Li Zhenyou, Vinayan Bhaghavathi Parambath, Diemant Thomas, Behm Rolf Jürgen, Fichtner Maximilian, Zhao-Karger Zhirong
Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstraße 11, Ulm, D-89081, Germany.
Institute of Surface Chemistry and Catalysis, Ulm University, Albert-Einstein-Allee 47, Ulm, D-89081, Germany.
Small. 2020 Oct;16(39):e2001806. doi: 10.1002/smll.202001806. Epub 2020 Aug 18.
Rechargeable metal-sulfur batteries show great promise for energy storage applications because of their potentially high energy and low cost. The multivalent-metal based electrochemical system exhibits the particular advantage of the feasibility of dendrite-free metal anode. Calcium (Ca) represents a promising anode material owing to the low reductive potential, high capacity, and abundant natural resources. However, calcium-sulfur (Ca-S) battery technology is in an early R&D stage, facing the fundamental challenge to develop a suitable electrolyte enabling reversible electrochemical Ca deposition, and at the same time, sulfur redox reactions in the system. Herein, a study of a room-temperature Ca-S battery by employing a stable and efficient calcium tetrakis(hexafluoroisopropyloxy) borate Ca[B(hfip) ] electrolyte is presented. The Ca-S batteries exhibit a cell voltage of ≈2.1 V (close to its thermodynamic value) and good reversibility. The mechanistic studies hint at a redox chemistry of sulfur with polysulfide/sulfide species involved in the Ca-based system.
可充电金属硫电池因其潜在的高能量和低成本,在储能应用方面展现出巨大潜力。基于多价金属的电化学系统具有无枝晶金属阳极可行性的特殊优势。钙(Ca)由于其低还原电位、高容量和丰富的自然资源,是一种很有前景的阳极材料。然而,钙硫(Ca-S)电池技术仍处于早期研发阶段,面临着开发一种合适的电解质以实现可逆电化学钙沉积以及同时实现系统中硫氧化还原反应的根本挑战。在此,本文介绍了一项通过使用稳定且高效的四(六氟异丙氧基)硼酸钙Ca[B(hfip)₄]电解质对室温Ca-S电池进行的研究。该Ca-S电池表现出约2.1 V的电池电压(接近其热力学值)和良好的可逆性。机理研究表明,在钙基体系中,硫与多硫化物/硫化物物种存在氧化还原化学过程。