TY - JOUR
T1 - Stabilizing undercoordinated single-atom Pdδ+ sites on CeO2-x nano-island for efficient hydrogenation of nitrile butadiene rubber
AU - He, Jiaxin
AU - Zhou, Shangqi
AU - Guo, Lisha
AU - An, Siying
AU - Bai, Rui
AU - Ma, Wenxiu
AU - Lin, Jin
AU - Zhang, Jichao
AU - Yuan, Menglei
AU - Zhang, Jian
N1 - Publisher Copyright:
© 2026 Institute of Process Engineering, Chinese Academy of Sciences
PY - 2026
Y1 - 2026
N2 - Palladium single-atom catalysts show exceptional catalytic performance in nitrile butadiene rubber (NBR) hydrogenation due to their unique unsaturated coordination environments. However, the hydrogenation activity and atomic efficiency are seriously limited by inherent instability of undercoordinated Pdδ+ sites and poor support structure, leading to decreased hydrogenation degree and cycling stability. In this work, a novel single-atom palladium catalysts was developed, where undercoordinated single-atom Pdδ+ sites are steadily anchored onto CeO2-x nano-islands supported by SiO2 (Pd1/CeO2-x/SiO2). The strong metal-interaction of CeO2-x nano-islands immobilize the undercoordinated Pdδ+ sites to enhance adsorption of olefin bonds in NBR, while SiO2 promotes mass transfer diffusion of NBR and atomic efficiency of palladium. The Pd1/CeO2-x/SiO2 thus achieves an unprecedented hydrogenation degree of up to 99.8% without decrease over a 10-runs stability test in selective hydrogenation of NBR, outperforming previously state-of-the-art catalysts. Consequently, this work will offer a new strategy for single-atom catalysts to achieve high steady-state activity in selective hydrogenation.
AB - Palladium single-atom catalysts show exceptional catalytic performance in nitrile butadiene rubber (NBR) hydrogenation due to their unique unsaturated coordination environments. However, the hydrogenation activity and atomic efficiency are seriously limited by inherent instability of undercoordinated Pdδ+ sites and poor support structure, leading to decreased hydrogenation degree and cycling stability. In this work, a novel single-atom palladium catalysts was developed, where undercoordinated single-atom Pdδ+ sites are steadily anchored onto CeO2-x nano-islands supported by SiO2 (Pd1/CeO2-x/SiO2). The strong metal-interaction of CeO2-x nano-islands immobilize the undercoordinated Pdδ+ sites to enhance adsorption of olefin bonds in NBR, while SiO2 promotes mass transfer diffusion of NBR and atomic efficiency of palladium. The Pd1/CeO2-x/SiO2 thus achieves an unprecedented hydrogenation degree of up to 99.8% without decrease over a 10-runs stability test in selective hydrogenation of NBR, outperforming previously state-of-the-art catalysts. Consequently, this work will offer a new strategy for single-atom catalysts to achieve high steady-state activity in selective hydrogenation.
KW - CeO nano-island
KW - Nitrile butadiene rubber
KW - Single-atom catalyst
KW - Undercoordinated Pd site
UR - https://www.scopus.com/pages/publications/105046349849
U2 - 10.1016/j.gce.2026.07.004
DO - 10.1016/j.gce.2026.07.004
M3 - 文章
AN - SCOPUS:105046349849
SN - 2096-9147
JO - Green Chemical Engineering
JF - Green Chemical Engineering
ER -