Yan Wei, Xing Qianli, Ren Jianwei, Feng Hao, Yu Jinshi, Liu Hao, Chen Wenmiao, Wang Kang, Chen Yanli
School of Materials Science and Engineering, China University of Petroleum (East China), Qingdao, 266580, P. R. China.
Department of Chemistry and Chemical Engineering, University of Science and Technology Beijing, Beijing, 100083, P. R. China.
Small. 2024 Apr;20(14):e2308473. doi: 10.1002/smll.202308473. Epub 2023 Nov 16.
Decorating platinum (Pt) with a single atom offers a promising approach to tailoring their catalytic activity. In this study, for the first time, an innovative assistive active sites (AAS) strategy is proposed to construct high-loading (3.46wt.%) single Fe─N as AAS, which are further hybridized with small Pt nanoparticles to enhance both oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR) activities. For ORR, the target catalyst (Pt/HFe-HCS) exhibits a higher mass activity (MA) of 0.98 A mg and specific activity (SA) of 1.39 mA cm at 0.90 V versus RHE. As for MOR, Pt/HFe-HCS shows exceptional MA (3.21 A mg ) and SA (4.27 mA cm ) at peak values, surpassing commercial Pt/C by 15.3 and 11.5 times, respectively. The underlying mechanism behind this AAS strategy is to find that in MOR, Fe─N promotes water dissociation, generating more *OH to accelerate the conversion of *CO to CO. Meanwhile, in ORR, Fe─N acts as a competitor to adsorb *OH, weakening Pt─OH bonding and facilitating desorption of *OH on the Pt surface. Constructing AAS that can enhance dual functionality simultaneously can be seen as a successful "kill two birds with one stone" strategy.
用单原子修饰铂(Pt)为定制其催化活性提供了一种很有前景的方法。在本研究中,首次提出了一种创新的辅助活性位点(AAS)策略,以构建高负载量(3.46wt.%)的单原子Fe─N作为AAS,并将其与小尺寸的Pt纳米颗粒进一步杂化,以增强氧还原反应(ORR)和甲醇氧化反应(MOR)的活性。对于ORR,目标催化剂(Pt/HFe-HCS)在相对于可逆氢电极(RHE)为0.90V时,表现出较高的质量活性(MA)为0.98A mg 和比活性(SA)为1.39mA cm 。至于MOR,Pt/HFe-HCS在峰值处显示出优异的MA(3.21A mg )和SA(4.27mA cm ),分别比商业Pt/C高出15.3倍和11.5倍。这种AAS策略背后的潜在机制是发现在MOR中,Fe─N促进水的解离,产生更多的OH以加速CO向CO的转化。同时,在ORR中,Fe─N作为竞争者吸附OH,削弱Pt─OH键并促进OH在Pt表面的脱附。构建能够同时增强双重功能的AAS可被视为一种成功的“一石二鸟”策略。