4.7 Article

A ball milling method for highly dispersed Ni atoms on g-C3N4 to boost CO2 photoreduction

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 630, Issue -, Pages 290-300

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.10.110

Keywords

Ball milling method; Highly dispersed Ni atoms; Catalytic active sites; Photo-excited electrons; Enhanced CO2 photoreduction

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In this study, a high-energy ball milling method was used to fabricate single-atom nickel loaded on the surface of g-C3N4 catalyst, and the loading amount was optimized. The results showed that the uniform dispersion of single-atom nickel played a decisive role in enhancing catalytic performance. This study provides guidance for the design of photocatalysts with highly dispersed single-atom catalytic active sites.
Atomically dispersed active sites can effectively enhance the catalytic activity, but the synthesis of highly dispersed single-atom active sites remains challenging. Herein, we report for the fabrication of singleatom Ni on g-C3N4 (CN) catalysts for photocatalytic CO2 reduction reaction (CO2RR) using a high-energy ball milling method. The uniformly loaded single-atomic Ni on the surface of the substrate suggests the improvement of synthetic methods. After optimizing the Ni loading, the photocatalyst containing 0.5 at% (0.32 wt%) single-atomic Ni (Ni/CN-0.5) exhibited the highest CO2 reduction performance (similar to 19.9 mu mol.g(-1).h(-1)) without any co-catalyst or sacrificial agent. As visualized by aberration-corrected high-angle annular darkfield scanning transmission electron microscopy (AC HAADF-STEM), the Ni atoms in the Ni/CN-0.5 photocatalyst are most uniformly dispersed for different loadings (0.1, 0.3, 0.5, 0.7, 1.0, 3.0 and 5.0 at%). These results suggest that the uniformity of the single-atom active sites plays a decisive role rather than the loading amount in the highly enhanced performance. This work provides insight into the design of photocatalysts with highly dispersed single-atom catalytic active sites for enhancing activity. (C) 2022 Elsevier Inc. All rights reserved.

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