Chen Kejun, Liu Kang, An Pengda, Li Huangjingwei, Lin Yiyang, Hu Junhua, Jia Chuankun, Fu Junwei, Li Hongmei, Liu Hui, Lin Zhang, Li Wenzhang, Li Jiahang, Lu Ying-Rui, Chan Ting-Shan, Zhang Ning, Liu Min
State Key Laboratory of Powder Metallurgy, School of Physical and Electronics, Central South University, Changsha, 410083, China.
School of Materials Science and Engineering, Central South University, Changsha, 410083, China.
Nat Commun. 2020 Aug 20;11(1):4173. doi: 10.1038/s41467-020-18062-y.
Iron phthalocyanine (FePc) is a promising non-precious catalyst for the oxygen reduction reaction (ORR). Unfortunately, FePc with plane-symmetric FeN site usually exhibits an unsatisfactory ORR activity due to its poor O adsorption and activation. Here, we report an axial Fe-O coordination induced electronic localization strategy to improve its O adsorption, activation and thus the ORR performance. Theoretical calculations indicate that the Fe-O coordination evokes the electronic localization among the axial direction of O-FeN sites to enhance O adsorption and activation. To realize this speculation, FePc is coordinated with an oxidized carbon. Synchrotron X-ray absorption and Mössbauer spectra validate Fe-O coordination between FePc and carbon. The obtained catalyst exhibits fast kinetics for O adsorption and activation with an ultralow Tafel slope of 27.5 mV dec and a remarkable half-wave potential of 0.90 V. This work offers a new strategy to regulate catalytic sites for better performance.
铁酞菁(FePc)是一种很有前景的用于氧还原反应(ORR)的非贵金属催化剂。不幸的是,具有平面对称FeN位点的FePc由于其较差的氧吸附和活化能力,通常表现出不尽人意的ORR活性。在此,我们报道了一种轴向Fe-O配位诱导的电子局域化策略,以改善其氧吸附、活化以及ORR性能。理论计算表明,Fe-O配位引发了O-FeN位点轴向之间的电子局域化,从而增强了氧吸附和活化。为了实现这一推测,将FePc与氧化的碳进行配位。同步辐射X射线吸收和穆斯堡尔光谱验证了FePc与碳之间的Fe-O配位。所获得的催化剂表现出快速的氧吸附和活化动力学,具有27.5 mV dec的超低塔菲尔斜率和0.90 V的显著半波电位。这项工作提供了一种调节催化位点以实现更好性能的新策略。