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Tensile-Strained Holey Pd Metallene toward Efficient and Stable Electrocatalysis
Tiantian Zeng1, Xiaomin Meng1, Shiwei Sun1
1Institute of Materials for Energy and Environment, Institute of Biochemical Engineering, College of Materials Science and Engineering, Qingdao University, Qingdao, 266071, P. R. China.
This study reports a new method for creating tensile-strained, holey palladium (Pd) metallenes. These novel structures show improved catalytic activity and stability for energy applications like oxygen reduction reactions.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Noble metal-based metallenes are crucial for energy catalysis.
- Controlling metallene surface structures for enhanced catalytic properties is challenging due to their instability.
Purpose of the Study:
- To synthesize tensile-strained, holey palladium (Pd) metallene with precisely controlled surface structures.
- To investigate the enhanced catalytic activity and stability of the synthesized metallene for energy conversion reactions.
Main Methods:
- Synthesis of tensile-strained, holey Pd metallene via oxidative etching using hydrogen peroxide.
- Utilizing pre-prepared Pd metallene as a catalyst to decompose hydrogen peroxide.
- Preferential removal of Pd atoms in amorphous regions during the etching process.
Main Results:
- The synthesized tensile-strained, holey Pd metallene exhibits significantly enhanced catalytic activity and stability compared to normal Pd metallene.
- The material shows improved performance in both oxygen reduction reaction (ORR) and formic acid oxidation.
- Enhanced ORR activity is attributed to the electrostatic repulsion between intermediate O* and dopant O, weakening the adsorption energy of O*.
Conclusions:
- A facile and economical strategy for precisely shaping metallene-based nanoarchitectures has been developed.
- The tensile-strained, holey Pd metallene offers broad applications in energy systems and sensing devices.
- This approach provides a pathway to overcome the limitations of intrinsic thermodynamic instability in metallenes for catalysis.
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