Song Ailing, Zhao Jinghao, Qiao Chunting, Ding Yali, Tian Guoxing, Fan Yuqian, Ma Zhipeng, Dai Lei, Shao Guangjie, Liu Zhaoping
Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China; State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China.
Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China.
J Colloid Interface Sci. 2024 Nov 15;674:336-344. doi: 10.1016/j.jcis.2024.06.170. Epub 2024 Jun 24.
Sluggish kinetics and severe structural instability of manganese-based cathode materials for rechargeable aqueous zinc-ion batteries (ZIBs) lead to low-rate capacity and poor cyclability, which hinder their practical applications. Pillaring manganese dioxide (MnO) by pre-intercalation is an effective strategy to solve the above problems. However, increasing the pre-intercalation content to realize stable cycling of high capacity at large current densities is still challenging. Here, high-rate aqueous Zn storage is realized by a high-capacity K-pillared multi-nanochannel MnO cathode with 1 K per 4 Mn (δ-KMnO). The high content of the K pillar, in conjunction with the three-dimensional confinement effect and size effect, promotes the stability and electron transport of multi-nanochannel layered MnO in the ion insertion/removal process during cycling, accelerating and accommodating more Zn diffusion. Multi-perspective in/ex-situ characterizations conclude that the energy storage mechanism is the Zn/H ions co-intercalating and phase transformation process. More specifically, the δ-KMnO nanospheres cathode delivers an ultrahigh reversible capacity of 297 mAh g at 1 A g for 500 cycles, showing over 96 % utilization of the theoretical capacity of δ-MnO. Even at 3 A g, it also delivered a 63 % utilization and 64 % capacity retention after 1000 cycles. This study introduces a highly efficient cathode material based on manganese oxide and a comprehensive analysis of its structural dynamics. These findings have the potential to improve energy storage capabilities in ZIBs significantly.
用于可充电水系锌离子电池(ZIBs)的锰基正极材料动力学迟缓且结构严重不稳定,导致低倍率容量和较差的循环稳定性,这阻碍了它们的实际应用。通过预嵌入对二氧化锰(MnO)进行柱撑是解决上述问题的有效策略。然而,增加预嵌入含量以实现在大电流密度下的高容量稳定循环仍然具有挑战性。在此,通过每4个Mn含有1个K的高容量K柱撑多纳米通道MnO正极(δ-KMnO)实现了高倍率水系锌存储。高含量的K柱,结合三维限域效应和尺寸效应,在循环过程中的离子嵌入/脱出过程中促进了多纳米通道层状MnO的稳定性和电子传输,加速并容纳了更多的锌扩散。多视角的原位/非原位表征得出,储能机制是Zn/H离子共嵌入和相变过程。更具体地说,δ-KMnO纳米球正极在1 A g下循环500次时提供了297 mAh g的超高可逆容量,显示出δ-MnO理论容量的96%以上的利用率。即使在3 A g下,在1000次循环后它也实现了63%的利用率和64%的容量保持率。本研究介绍了一种基于氧化锰的高效正极材料,并对其结构动力学进行了全面分析。这些发现有可能显著提高水系锌离子电池的储能能力。