Liu Ming, Wang Xuemin, Cao Shoufu, Lu Xiaoqing, Li Wei, Li Na, Bu Xian-He
School of Materials Science and Engineering, Nankai University, Tianjin, 300350, China.
School of Materials Science and Engineering, China University of Petroleum, Qingdao, 266580, China.
Adv Mater. 2024 May;36(19):e2309231. doi: 10.1002/adma.202309231. Epub 2024 Feb 20.
Dual-metal center catalysts (DMCs) have shown the ability to enhance the oxygen reduction reaction (ORR) owing to their distinctive structural configurations. However, the precise modulation of electronic structure and the in-depth understanding of synergistic mechanisms between dual metal sites of DMCs at the atomic level remain challenging. Herein, mimicking the ferredoxin, Fe-based DMCs (FeN-S) are strategically designed and fabricated, in which additional Fe and S sites are synchronously installed near the Fe sites and serve as "dual modulators" for coarse- and fine-tuning of the electronic modulation, respectively. The as-prepared FeN-S catalyst exhibits enhanced ORR activity and outstanding Zinc-air (Zn-air) battery performance compared to the conventional single Fe site catalysts. The theoretical and experimental results reveal that introducing the second metal Fe creates a dual adsorption site that alters the O adsorption configuration and effectively activates the O─O bond, while the synergistic effect of dual Fe sites results in the downward shift of the d-band center, facilitating the release of OH*. Additionally, local electronic engineering of heteroatom S for Fe sites further facilitates the formation of the rate-determining step OOH*, thus accelerating the reaction kinetics.
双金属中心催化剂(DMCs)因其独特的结构构型展现出增强氧还原反应(ORR)的能力。然而,在原子水平上对DMCs双金属位点之间电子结构的精确调控以及协同机制的深入理解仍然具有挑战性。在此,模仿铁氧化还原蛋白,策略性地设计并制备了基于铁的DMCs(FeN-S),其中额外的铁和硫位点分别在铁位点附近同步安装,分别作为电子调制粗调和微调的“双调制器”。与传统的单铁位点催化剂相比,所制备的FeN-S催化剂表现出增强的ORR活性和出色的锌空气(Zn-air)电池性能。理论和实验结果表明,引入第二种金属铁会产生一个双吸附位点,改变氧的吸附构型并有效激活O─O键,而双铁位点的协同效应导致d带中心向下移动,促进OH的释放。此外,对铁位点进行杂原子硫的局部电子工程进一步促进了速率决定步骤OOH的形成,从而加速了反应动力学。