Mo₂TiC₂Tₓ MXeneにおける逐次表面工学による白金単原子固定メカニズムの解明
Bo-Heng Huang1, Wen-Hsuan Liao2, Shih-Wen Tseng3
1Department of Chemistry, National Cheng Kung University, No. 1, University Road, East District, Tainan 701, Taiwan. iwchen1978@gs.ncku.edu.tw.
Abstract:
A tunable electroreduction strategy enables sequential surface engineering of Mo2TiC2Tx MXene, identifying Mo atomic vacancies as the primary anchoring sites for Pt single atoms. This work establishes vacancy-directed MXene functionalization as an effective platform for single-atom catalysis.
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