Scientists Identify Electronic and Structural Dynamics of Catalytic Centers in Single-Fe-Atom Material
Single-atom catalyst (SAC) is a conceptual bridge between homo- and heterogeneous catalysis. It offers new opportunities for capturing the reaction intermediates by identifying the active sites, and even monitoring the dynamic behaviors of both the geometric structure and electronic environment of the catalytic sites at atomic scale.
To achieve this goal, both the exploration of model SACs with definite microenvironment and the development of novel operando techniques with high atomic resolution are of great significance, however, it is still challenging.
Recently, a research team led by Prof. HUANG Yanqiang and Prof. ZHANG Tao from the Dalian Institute of Chemical Physics (DICP) of the Chinese Academy of Sciences (CAS), in collaboration with Prof. WANG Junhu from DICP, Prof. LIU Bin from Nanyang Technological University of Singapore, and Prof. LI Jun from Tsinghua University reported their findings on electronic and structural dynamics of catalytic centers in single-Fe-atom material under in situ oxygen reduction reaction (ORR) conditions.
The result was published in Chem on November 20.
The identification of the electronic and structural dynamics of catalytic centers in single-Fe-atom material by Operando Mossbauer spectroscopy (Image by LI Xuning)
In this study, researchers synthesized single-Fe-atom catalysts with well-controlled site density and definite N-coordination environment via a solvent-assisted linker exchange (SALE) method. They used it as model systems for electronic-level understanding of the ORR mechanism.
"We developed Operando Mossbauer spectroscopy for the first time to identify the exact structures and spin state of active atomically dispersed Fe moieties during ORR," said Prof. HUANG.
By combining with operando Raman and X-ray absorption spectroscopy (XAS) measurements, as well as density functional theory (DFT) studies, it was evidenced that the potential-relevant structural and electronic evolutions of the active single-Fe-atom moieties were via directly capturing the *O2- and *OH- intermediates under ORR conditions.
These results provided a proof of concept for the integration of operando techniques and SACs, which might direct the way toward the electronic-level insight into the catalytic centers and reaction mechanism.
The research was supported by the National Key Projects for Fundamental Research and Development of China, the Strategic Priority Research Programme of the CAS.
Dalian Institute of Chemical Physics, Chinese Academy of Sciences
457 Zhongshan Road, Dalian, 116023, China
Tel: 86-411-84374221
E-mail: wangyj@dicp.ac.cn
