TY - JOUR
T1 - Heterogeneous single-atom photocatalysts for oxidative Heck reactions
AU - Zhou, Xue
AU - Tong, Shijun
AU - Zhang, Zhonghai
N1 - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Photocatalytic synthesis has emerged as a promising green synthetic approach. The development of ideal heterogeneous photocatalysts is crucial for expanding the scope of photocatalytic reactions. Single-atom catalysts (SACs), with their exceptional atomic efficiency and catalytic performance, have garnered significant attention. Herein, we employed cost-effective organic semiconductor g-C3N4 as a support for single-atom catalysts. Palladium (Pd) single-atom photocatalysts (Pd1/g-C3N4) were synthesized via a freeze-electrochemical reduction method and applied to the oxidative Heck reaction. In this system, g-C3N4 acts as both a photosensitizer and a stabilizing matrix for single atoms, while the anchored Pd atoms serve as catalytic active sites. By optimizing the loading of Pd single atoms, a 70% conversion yield was achieved under visible light irradiation at room temperature, surpassing the performance of homogeneous transition metal catalysts. Furthermore, the heterogeneous photocatalysts demonstrated excellent recyclability over multiple cycles. Ni1/g-C3N4 also exhibited moderate catalytic efficiency, highlighting its potential as a low-cost alternative. This work provides a sustainable strategy for constructing C-C bonds under mild conditions and paves the way for industrial-scale applications.
AB - Photocatalytic synthesis has emerged as a promising green synthetic approach. The development of ideal heterogeneous photocatalysts is crucial for expanding the scope of photocatalytic reactions. Single-atom catalysts (SACs), with their exceptional atomic efficiency and catalytic performance, have garnered significant attention. Herein, we employed cost-effective organic semiconductor g-C3N4 as a support for single-atom catalysts. Palladium (Pd) single-atom photocatalysts (Pd1/g-C3N4) were synthesized via a freeze-electrochemical reduction method and applied to the oxidative Heck reaction. In this system, g-C3N4 acts as both a photosensitizer and a stabilizing matrix for single atoms, while the anchored Pd atoms serve as catalytic active sites. By optimizing the loading of Pd single atoms, a 70% conversion yield was achieved under visible light irradiation at room temperature, surpassing the performance of homogeneous transition metal catalysts. Furthermore, the heterogeneous photocatalysts demonstrated excellent recyclability over multiple cycles. Ni1/g-C3N4 also exhibited moderate catalytic efficiency, highlighting its potential as a low-cost alternative. This work provides a sustainable strategy for constructing C-C bonds under mild conditions and paves the way for industrial-scale applications.
UR - https://www.scopus.com/pages/publications/105004901026
U2 - 10.1039/d5cy00356c
DO - 10.1039/d5cy00356c
M3 - 文章
AN - SCOPUS:105004901026
SN - 2044-4753
VL - 15
SP - 3660
EP - 3666
JO - Catalysis Science and Technology
JF - Catalysis Science and Technology
IS - 12
ER -