Yan Jiaxing, Yi Xiankai, Zhao Wei, Zheng Yifeng
College of Materials Science and Engineering, Nanjing Tech University, No. 30 Puzhu Road(S), Nanjing, Jiangsu 211816, PR China.
ACS Appl Mater Interfaces. 2025 Aug 5. doi: 10.1021/acsami.5c10617.
Zinc-air batteries (ZABs) have great promise for sustainable energy storage. However, the energy conversion efficiency is limited by the lack of cost-effective bifunctional catalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Herein, a nonmetallic phosphorus doping strategy in the B-site of MnCoO spinel catalyst via a scalable self-propagating combustion synthesis is developed for ZABs. The optimized MnCoPO catalyst exhibits exceptional bifunctional activity at 0.1 M KOH, achieving a positive half-wave potential of 0.80 V vs RHE for ORR alone with superior long-term stability (91.92% current density retention after 15000s), and an overpotential of 430 mV at 10 mA cm for OER, which is comparable to commercial Pt/C-RuO catalysts. Moreover, when the MnCoPO applied as the air electrode of ZABs, the ZABs enable a high peak power density of 152 mW cm and stable cycling over 120 h at 10 mA cm. Interestingly, phosphorus doping significantly increases the oxygen vacancy concentration and optimizes the Co/Co ratio with elevated e orbital occupancy, synergistically enhancing O activation and charge transfer, alongside a 2.5-fold increase in surface area (from 6.88 to 17.25 m g). This study indicates the critical role of electronic vacancy synergy in boosting bifunctional oxygen electrocatalysis, providing a generalizable strategy for spinel-type transition metal oxides in ZABs.
锌空气电池(ZABs)在可持续储能方面具有巨大潜力。然而,能量转换效率受到用于氧还原反应(ORR)和析氧反应(OER)的缺乏成本效益的双功能催化剂的限制。在此,通过可扩展的自蔓延燃烧合成法,开发了一种在MnCoO尖晶石催化剂的B位进行非金属磷掺杂的策略用于锌空气电池。优化后的MnCoPO催化剂在0.1 M KOH中表现出优异的双功能活性,对于ORR单独实现相对于可逆氢电极(RHE)为0.80 V的正半波电位,具有出色的长期稳定性(15000秒后电流密度保持率为91.92%),并且对于OER在10 mA cm时过电位为430 mV,这与商业Pt/C-RuO催化剂相当。此外,当MnCoPO用作锌空气电池的空气电极时,锌空气电池在10 mA cm时能够实现152 mW cm的高峰值功率密度和超过120小时的稳定循环。有趣的是,磷掺杂显著增加了氧空位浓度并优化了Co/Co比例,同时提高了e轨道占有率,协同增强了O活化和电荷转移,表面积增加了2.5倍(从6.88增加到17.25 m g)。这项研究表明电子空位协同作用在促进双功能氧电催化中的关键作用,为锌空气电池中的尖晶石型过渡金属氧化物提供了一种可推广的策略。