Sun Siyuan, Wei Kexin, Yang Fan, Sun Yang, An Junpu, Li Yongfeng
State Key Laboratory of Heavy Oil Processing, China University of Petroleum (Beijing), Changping, 102249, China.
State Key Laboratory of Heavy Oil Processing, China University of Petroleum (Beijing), Changping, 102249, China.
J Colloid Interface Sci. 2025 Sep 4;702(Pt 2):138925. doi: 10.1016/j.jcis.2025.138925.
Carbon-based catalysts with free-standing structure are essential for rechargeable zinc-air battery as electrodes, which can avoid the side effects brought by organic binder. However, the current preparation methods still can be improved for faster preparation process and morphology control. In this study, we reported a fabrication strategy of self-standing carbon catalyst loaded with CoFe nanoparticles and carbon nanotube as air electrodes for liquid rechargeable zinc-air battery. With a rapidly prepared PAN film used as substrate, ZIF with both Fe and Co elements are loading as active site precursor, which a composite structure of CoFe nanoparticles and carbon nanotube will form on the free-standing catalyst surface after the carbonization process. In this structure, the carbonated PAN film substrate will provide rich conductive paths to promote electron transfer during the reaction process, and the active sites on the surface can promote the contact between intermediates and active sites. The optimized catalyst FeCo@CP-1:1 has the best ORR/OER bifunctional catalytic activity, which exhibits a halfwave potential (E) of 0.89 V (vs. RHE) for the ORR and a potential of 1.47 V at a current density of 10 mA cm (E) for the OER. It can be attributed to the excellent ORR catalytic activity of CoFe nanoparticles and its reconstruction process in OER. Furthermore, FeCo@CP-1:1 exhibits a power density of 154 mW cm and long cyclic stability in liquid ZABs application. This research lays a practical foundation for design and synthesis of free-standing carbon catalyst.
具有自支撑结构的碳基催化剂作为可充电锌空气电池的电极至关重要,它可以避免有机粘合剂带来的副作用。然而,目前的制备方法在制备过程的速度和形态控制方面仍有改进空间。在本研究中,我们报道了一种负载有钴铁纳米颗粒和碳纳米管的自支撑碳催化剂的制备策略,用于液态可充电锌空气电池的空气电极。以快速制备的聚丙烯腈(PAN)薄膜为基底,负载同时含有铁和钴元素的沸石咪唑酯骨架结构材料(ZIF)作为活性位点前驱体,经过碳化过程后,在自支撑催化剂表面将形成钴铁纳米颗粒和碳纳米管的复合结构。在这种结构中,碳化的PAN薄膜基底将提供丰富的导电路径,以促进反应过程中的电子转移,并且表面的活性位点可以促进中间体与活性位点之间的接触。优化后的催化剂FeCo@CP-1:1具有最佳的氧还原反应(ORR)/析氧反应(OER)双功能催化活性,其ORR的半波电位(E)为0.89 V(相对于可逆氢电极,RHE),在电流密度为10 mA cm²(E)时OER的电位为1.47 V。这可归因于钴铁纳米颗粒优异的ORR催化活性及其在OER中的重构过程。此外,FeCo@CP-1:1在液态锌空气电池应用中表现出154 mW cm²的功率密度和长期循环稳定性。该研究为自支撑碳催化剂的设计与合成奠定了实际基础。