Single-atom Al precisely modulate the strain of Pt3Co intermetallic for superior oxygen catalytic performance

被引:11
作者
Wu, Wei [1 ]
Qu, Wei [2 ]
Wang, Zichen [1 ]
Tan, Yangyang [1 ]
Chen, Runzhe [1 ]
Chen, Suhao [1 ]
Lv, Haifeng [2 ]
Zhong, Jun [3 ]
Cheng, Niancai [1 ]
机构
[1] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350108, Peoples R China
[2] Shenzhen Acad Aerosp Technol, PEM Fuel Cell Catalyst Res & Dev Ctr, Shenzhen 518057, Peoples R China
[3] Soochow Univ, Inst Funct Nano & Soft Mat Lab FUNSOM, Jiangsu Key Lab Adv Negat Carbon Technol, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Single-atom; Strain engineering; Pt-based intermetallic; Oxygen reduction reaction; Atomic layer deposition; TOTAL-ENERGY CALCULATIONS; TRANSITION-METALS; REDUCTION; NANOPARTICLES; PLATINUM; ELECTROCATALYSTS; SHELL;
D O I
10.1016/j.cej.2024.151987
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Precisely controlling the strain of Pt-based intermetallic to ensure high performance and stability is a massive task for sustainable proton-exchange-membrane-fuel-cells. Herein, the Al single-atom was trapped into the L1(2)Pt(3)Co intermetallic core to precisely tailor the strain state on the Pt-skin for fast oxygen reduction reaction kinetics. Theoretical calculations firstly predicted that only tailored tension can accelerate the protonation of O-2 on L1(2)-Pt3Co@Pt without creating an additional energy barrier for subsequent oxygen-containing intermediates desorption. Experimentally, Al single-atom confined in the L1(2)-Pt3Co lattice by substituting partial Co occupancy, imposing tailored similar to 0.2 % tension on Pt-skin compared to the L1(2-)Pt(3)Co. L1(2)-Al-Pt3Co@Pt/C exhibits enhanced mass activity which is ten-time improvement over commercial Pt/C. More significantly, XAS and DFT results reveal that the Al single-atom can strengthen the Pt-Co bonding, enhancing the stability of L1(2)-AlPt3Co@Pt/C in oxygen reduction. This work provides an avenue to design the strain by single-atom for sustainable energy conversion technologies.
引用
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页数:11
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