SinoGreenTech Academic Portal
LC
Verified CAS / Academic Author2 Decoded Studies

Prof. LENG Chengrang

University of Science and Technology of China

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3698-5

Identifying the Surface Dynamic Evolution of Electrocatalysts during Oxygen Evolution Reaction by In Situ Techniques

The oxygen evolution reaction (OER) is a critical bottleneck in next-generation sustainable energy systems due to its sluggish kinetics. Developing cost-effective, high-efficiency electrocatalysts requires understanding the dynamic structural evolution at electrode-electrolyte interfaces under operating conditions. In situ techniques are invaluable for identifying active centers and monitoring key intermediates. This review comprehensively summarizes recent advances in cutting-edge in situ methods for characterizing OER electrocatalyst structure evolution. It provides a brief overview of active motifs and robust structures using multiple in situ correlative techniques, establishing essential structure-performance relationships and updating mechanistic understanding at atomic scale under realistic conditions. Key challenges and perspectives are highlighted to promote rational design of promising electrocatalysts for efficient oxygen-associated electrocatalysis and electrosynthesis.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3527-x

Spatial Heteroatom Modulates Electron Itinerancy of Spinel Lattice for Accelerated Oxygen Catalysis

Heteroatom occupancy is pivotal for modulating specific material regions by introducing foreign elements into the host matrix, yet its spatial dimension remains underexplored. We introduce a 'satellite atom-spinel crystal' concept by synthesizing model catalysts with Fe atoms positioned at two distinct spatial locations of spinel Co3O4: satellite-Fe at Co3O4 (Fe(Sat)-Co3O4) and Fe-doped Co3O4 (Co3Fe(In)O4). Multidimensional in situ spectroscopies reveal that Fe(Sat)-Co3O4 overcomes the crystal field potential energy (FeSat–O > FeSat–O–CoOh) and exhibits 1% (Fe atom) lower impedance than Co3Fe(In)O4 due to a resistance-free electron delocalization layer formed in Fe(Sat)-Co3O4. This results in tens of times increase in turnover frequency and mass activity, and a 120 mV reduction in overpotential for the electrochemical oxygen evolution reaction compared to Co3Fe(In)O4. Density functional theory calculations dynamically elucidate the mechanisms governing electron itinerancy modulation. This study provides valuable insights into the impact of heteroatomic spatial positioning on material properties and significantly expands our understanding of atomic manipulation.