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Updated: Jun 5, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Oxygen vacancy mediated Pd-SA/TiO2 single-atom catalyst created via ultra-fast one-step synthesis for enhanced CO2
Yaru Zheng1, Wei Li2, Jie Ju1
1Key Laboratory for Ultrafine Materials of Ministry of Education, Shanghai Environmental, Friendly Materials Technical Service Platform, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Abstract:
Single-atom catalysts (SACs) have garnered considerable interest in the field of heterogeneous catalysis. This study detail the synthesis of single-atom Pd catalysts supported on metal oxides using the Flame Spray Pyrolysis (FSP) method. This technique allows for the preparation of TiO2 with abundant oxygen vacancies by incorporating a hydrogen-rich atmosphere at high temperature (>2000 K) utilizing the quenching ring, which enhances the catalyst synthesis process. Additionally, the distribution and electronic structure of Pd were tailored in a hydrogen-rich atmosphere, which promoted the entrapment of Pd atoms within oxygen vacancies, preventing their aggregation into Pd nanoparticles and leading to the formation of Pd-SA/TiO2. Notably, Pd-SA/TiO2 achieves 92.51 % CO2-to-CO selectivity in the photocatalytic CO2 reduction reaction and exhibits an impressive catalytic activity of 56.84μmol g-1h-1. This research introduces a novel approach to modulate the anchoring process and optimize the microenvironment for single-atom metal synthesis, advancing the development of the-state-of-the-art SACs.
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