TY - JOUR
T1 - Rational design of carbon–nitrogen based cluster catalysts for energy conversion applications
AU - Bai, Qian
AU - Sun, Zhiyi
AU - Jiang, Shuai
AU - Ma, Xiaolu
AU - Li, Runmin
AU - Shang, Huishan
AU - Chen, Wenxing
N1 - Publisher Copyright:
This journal is © The Royal Society of Chemistry, 2026
PY - 2026/1/22
Y1 - 2026/1/22
N2 - Atomically precise cluster catalysts, composed of supported metal or metal oxide clusters, have emerged as a rapidly developing frontier in heterogeneous catalysis, bridging the advantages of single-atom catalysts (SACs) and traditional metal nanoparticles. Among various supports, carbon nitride (CN)-based materials have attracted significant attention due to their tunable electronic structures, abundant coordination sites, and strong metal–support interactions. These features facilitate the stabilization of ultrasmall clusters with well-defined coordination environments and dynamic reactivity under operating conditions. This review systematically summarizes recent advances in CN-supported metal and metal oxide clusters for key energy conversion reactions, including the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reaction (HER), nitrate reduction reaction (NO3RR), and carbon dioxide reduction reaction (CO2RR). We emphasize how the synergistic effects among the cluster composition, size, synthesis strategy, and CN coordination environment govern catalytic activity and selectivity through charge redistribution and multi-site cooperation. Finally, current challenges and future opportunities in the rational design and structural stabilization of CN supported cluster catalysts are discussed, aiming to guide their further development toward practical applications in sustainable energy conversion.
AB - Atomically precise cluster catalysts, composed of supported metal or metal oxide clusters, have emerged as a rapidly developing frontier in heterogeneous catalysis, bridging the advantages of single-atom catalysts (SACs) and traditional metal nanoparticles. Among various supports, carbon nitride (CN)-based materials have attracted significant attention due to their tunable electronic structures, abundant coordination sites, and strong metal–support interactions. These features facilitate the stabilization of ultrasmall clusters with well-defined coordination environments and dynamic reactivity under operating conditions. This review systematically summarizes recent advances in CN-supported metal and metal oxide clusters for key energy conversion reactions, including the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reaction (HER), nitrate reduction reaction (NO3RR), and carbon dioxide reduction reaction (CO2RR). We emphasize how the synergistic effects among the cluster composition, size, synthesis strategy, and CN coordination environment govern catalytic activity and selectivity through charge redistribution and multi-site cooperation. Finally, current challenges and future opportunities in the rational design and structural stabilization of CN supported cluster catalysts are discussed, aiming to guide their further development toward practical applications in sustainable energy conversion.
UR - https://www.scopus.com/pages/publications/105025531967
U2 - 10.1039/d5cc06507k
DO - 10.1039/d5cc06507k
M3 - Review article
AN - SCOPUS:105025531967
SN - 1359-7345
VL - 62
SP - 1672
EP - 1691
JO - Chemical Communications
JF - Chemical Communications
IS - 6
ER -