Chao Dongliang, Ye Chao, Xie Fangxi, Zhou Wanhai, Zhang Qinghua, Gu Qinfen, Davey Kenneth, Gu Lin, Qiao Shi-Zhang
School of Chemical Engineering & Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
Beijing National Laboratory for Condensed Matter Physics Institute of Physics, Chinese Academy of Science, Beijing, 100190, China.
Adv Mater. 2020 Jun;32(25):e2001894. doi: 10.1002/adma.202001894. Epub 2020 May 19.
Research interest and achievements in zinc aqueous batteries, such as alkaline Zn//Mn, Zn//Ni/Co, Zn-air batteries, and near-neutral Zn-ion and hybrid ion batteries, have surged throughout the world due to their features of low-cost and high-safety. However, practical application of Zn-based secondary batteries is plagued by restrictive energy and power densities in which an inadequate output plateau voltage and sluggish kinetics are mutually accountable. Here, a novel paradigm high-rate and high-voltage Zn-Mn hybrid aqueous battery (HAB) is constructed with an expanded electrochemical stability window over 3.4 V that is affordable. As a proof of concept, catalyzed MnO /Mn electrolysis kinetics is demonstrated in the HAB via facile introduction of Ni into the electrolyte. Various techniques are employed, including in situ synchrotron X-ray powder diffraction, ex situ X-ray absorption fine structure, and electron energy loss spectroscopy, to reveal the reversible charge-storage mechanism and the origin of the boosted rate-capability. Density functional theory (DFT) calculations reveal enhanced active electron states and charge delocalization after introducing strongly electronegative Ni. Simulations of the reaction pathways confirm the enhanced catalyzed electrolysis kinetics by the facilitated charge transfer at the active O sites around Ni dopants. These findings significantly advance aqueous batteries a step closer toward practical low-cost application.
由于锌水系电池(如碱性Zn//Mn、Zn//Ni/Co、锌空气电池以及近中性锌离子和混合离子电池)具有低成本和高安全性的特点,全球范围内对其的研究兴趣和成果激增。然而,锌基二次电池的实际应用受到能量和功率密度受限的困扰,其中输出平台电压不足和动力学迟缓相互影响。在此,构建了一种新型的高倍率和高电压锌-锰混合水系电池(HAB),其具有超过3.4 V的可承受的扩展电化学稳定性窗口。作为概念验证,通过在电解液中简便引入镍,在HAB中展示了催化MnO /Mn的电解动力学。采用了各种技术,包括原位同步辐射X射线粉末衍射、非原位X射线吸收精细结构和电子能量损失谱,以揭示可逆电荷存储机制和倍率性能提升的起源。密度泛函理论(DFT)计算表明,引入强电负性的镍后,活性电子态增强且电荷离域。反应途径的模拟证实了通过镍掺杂剂周围活性O位点处电荷转移的促进,催化电解动力学得到增强。这些发现显著推动水系电池向实际低成本应用迈进了一步。