College of Chemistry and Chemical Engineering , Inner Mongolia University , Hohhot 010021 , P. R. China.
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry , Jilin University , Changchun 130022 , P. R. China.
ACS Appl Mater Interfaces. 2019 Oct 16;11(41):37531-37540. doi: 10.1021/acsami.9b10149. Epub 2019 Sep 19.
The exploration of robust multifunctional electrocatalyst for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is a continuing challenge for the sustainable energy sources. However, as the key reactions in renewable metal-air batteries and fuel cells, the energy conversion efficiencies of ORR and OER are greatly affected by their reaction kinetics. In addition to designing excellent electrocatalysts, new methods to stabilize the electrolyte/electrode interfaces are urgently needed. Herein, a hierarchical Co(OH)F/CuCoS hybrid was created as an efficient catalyst for OER and ORR in alkaline media. Combining spinel ferrite with the hydroxide can greatly boost their catalytic performance. The optimal Co(OH)F/CuCoS hybrid exhibits superior OER performance and durable stability, as demonstrated by an ultralow overpotential of 230 mV at 10 mA·cm. The onset potential and the half-wave potential in 0.1 M KOH solution for ORR are 0.88 and 0.80 V, respectively. Furthermore, the Co(OH)F/CuCoS hybrid served as a catalyst in Zn air batteries catalyst exhibits a low overpotential of 1.12 V at 50.0 mA·cm, large power density of 144 mW·cm, and a long electrochemical lifetime of 118 h (118 cycles), which is even better than those of the Pt/C and RuO catalysts. The rational integration of spinel and hydroxide at the interface can provide multifunctional electrocatalysis and possess a high reactivity for oxygen conversion. Synergistic coupling effect and interfacial electronic interaction between Co(OH)F and CuCoS can significantly enhance the electron transfer rate, and these synergistic advantages enable the heterogeneous structure of the multifunctional electrocatalyst to produce excellent catalytic performance.
用于氧还原反应(ORR)和氧析出反应(OER)的稳健多功能电催化剂的探索仍然是可持续能源的挑战。然而,作为可再金属-空气电池和燃料电池中的关键反应,ORR 和 OER 的能量转换效率受到其反应动力学的极大影响。除了设计出色的电催化剂外,还迫切需要新的方法来稳定电解质/电极界面。在此,作为碱性介质中 OER 和 ORR 的高效催化剂,构建了分级 Co(OH)F/CuCoS 杂化物。尖晶石铁氧体与氢氧化物的结合可以极大地提高它们的催化性能。优化的 Co(OH)F/CuCoS 杂化物具有出色的 OER 性能和持久稳定性,在 10 mA·cm 时的过电势低至 230 mV。在 0.1 M KOH 溶液中,ORR 的起始电位和半波电位分别为 0.88 和 0.80 V。此外,Co(OH)F/CuCoS 杂化物作为 Zn 空气电池催化剂,在 50.0 mA·cm 时的过电势低至 1.12 V,功率密度高达 144 mW·cm,电化学寿命长达 118 h(118 个循环),甚至优于 Pt/C 和 RuO 催化剂。尖晶石和氢氧化物在界面处的合理整合可以提供多功能电催化作用,具有高的氧气转化反应性。Co(OH)F 和 CuCoS 之间的协同耦合效应和界面电子相互作用可以显著提高电子转移速率,这些协同优势使多功能电催化剂的异质结构产生了出色的催化性能。