Li He, Wang Jihao, Tjardts Tim, Barg Igor, Qiu Haoyi, Müller Martin, Krahmer Jan, Askari Sadegh, Veziroglu Salih, Aktas Cenk, Kienle Lorenz, Benedikt Jan
Institute of Experimental and Applied Physics, Kiel University, Leibnizstraße 19, D-24098, Kiel, Germany.
Institute of Inorganic Chemistry, Kiel University, Max-Eyth-Straße 2/Otto-Hahn-Platz 6, D-24118., Kiel, Germany.
Small. 2024 Jun;20(24):e2310660. doi: 10.1002/smll.202310660. Epub 2024 Jan 2.
Designing an efficient, durable, and inexpensive bifunctional electrocatalyst toward oxygen evolution reactions (OER) and oxygen reduction reactions (ORR) remains a significant challenge for the development of rechargeable zinc-air batteries (ZABs). The generation of oxygen vacancies plays a vital role in modifying the surface properties of transition-metal-oxides (TMOs) and thus optimizing their electrocatalytic performances. Herein, a H/Ar plasma is employed to generate abundant oxygen vacancies at the surfaces of NiCoO nanowires. Compared with the Ar plasma, the H/Ar plasma generated more oxygen vacancies at the catalyst surface owing to the synergic effect of the Ar-related ions and H-radicals in the plasma. As a result, the NiCoO catalyst treated for 7.5 min in H/Ar plasma exhibited the best bifunctional electrocatalytic activities and its gap potential between E for OER and E for ORR is even smaller than that of the noble-metal-based catalyst. In situ electrochemical experiments are also conducted to reveal the proposed mechanisms for the enhanced electrocatalytic performance. The rechargeable ZABs, when equipped with cathodes utilizing the aforementioned catalyst, achieved an outstanding charge-discharge gap, as well as superior cycling stability, outperforming batteries employing noble-metal catalyst counterparts.
设计一种高效、耐用且廉价的用于析氧反应(OER)和氧还原反应(ORR)的双功能电催化剂,对于可充电锌空气电池(ZABs)的发展而言仍然是一项重大挑战。氧空位的产生在改变过渡金属氧化物(TMOs)的表面性质从而优化其电催化性能方面起着至关重要的作用。在此,采用H/Ar等离子体在NiCoO纳米线表面产生大量氧空位。与Ar等离子体相比,由于等离子体中Ar相关离子和H自由基的协同作用,H/Ar等离子体在催化剂表面产生了更多的氧空位。结果,在H/Ar等离子体中处理7.5分钟的NiCoO催化剂表现出最佳的双功能电催化活性,其OER的E和ORR的E之间的间隙电位甚至小于基于贵金属的催化剂。还进行了原位电化学实验以揭示所提出的增强电催化性能的机制。当配备使用上述催化剂的阴极时,可充电锌空气电池实现了出色的充放电间隙以及优异的循环稳定性,优于使用贵金属催化剂对应物的电池。