催化作用
水煤气变换反应
共沉淀
微晶
反向
材料科学
化学工程
工作(物理)
摩尔比
纳米棒
反应速率
草酸
反应条件
纳米技术
无机化学
化学
纳米颗粒
粒子(生态学)
多相催化
作者
Xihui Yang,Wanhui Feng,Xiujia Ma,Zihao Liu,Zijun Yang,Qingfeng Ge,Xinli Zhu
摘要
ABSTRACT The reverse water‐gas shift (RWGS) reaction can serve as a pivotal hub for converting CO 2 into value‐added chemicals. However, conventional Cu/CeO 2 catalysts are constrained by a limited metal‐oxide interfacial perimeter, suffering from both inadequate low‐temperature activity and poor stability. Herein, a series of CeO 2 /Cu‐x catalysts (where x is the Ce/Cu molar ratio) were synthesized via an oxalic acid‐assisted sol‐gel coprecipitation method, and tested for RWGS at 400°C and atmospheric pressure. The optimal inverse CeO 2 /Cu‐0.1 achieves an intrinsic reaction rate of 197.0 µmol·g cat −1 ·s −1 , which is 3.7 times higher than that of the conventional CeO 2 /Cu‐10 (53.1 µmol·g cat −1 ·s −1 ) and is much more stable. Structural analyses revealed that the CeO 2 /Cu‐0.1 is characterized by an inverse architecture of tiny CeO 2 crystallites (4.6 nm) on larger Cu particles (12.7 nm), which is distinct from conventional architecture of Cu clusters (3.3 nm) on larger CeO 2 particles (7.1 nm) for CeO 2 /Cu‐10. The inverse architecture significantly improves the density of Cu + ‐O V ‐Ce 3+ sites at the interfacial perimeter of CeO 2 /Cu, which facilitates the synergistic activation of H 2 and CO 2 as well as subsequent reaction, leading to lower reaction orders and a much higher intrinsic rate. This work demonstrates the inverse oxide/metal architecture with engineered oxide‐metal interfacial sites for enhancing RWGS.
科研通智能强力驱动
Strongly Powered by AbleSci AI