催化作用
煅烧
氧气
碳纤维
水煤气变换反应
集聚经济
化学工程
降水
材料科学
化学
无机化学
有机化学
物理
工程类
复合数
气象学
复合材料
作者
Jianhong Xu,Zihao Liu,Ruoyu Zhang,Qingfeng Ge,Xinli Zhu
标识
DOI:10.1002/asia.202401485
摘要
The reverse water gas shift (RWGS) reaction provides a convenient approach to convert CO2 to CO, which facilitates to achieve the goals of carbon peaking and carbon neutrality. Herein, the Cu/CeO2 catalyst prepared by a co‐precipitation method using a mixture of Na2CO3 and NaOH at pH of 10 (sample Cu/CeO2‐10) achieved an intrinsic reaction rate of 428.4 mmol•gcat‐1•h‐1 with 100% CO selectivity at 400 °C and CO2/H2 ratio of 1:4, which is much higher than Cu/CeO2 prepared by impregnation and other methods. Various characterizations showed the highest fraction of CuCeO2 solid solution in the calcined Cu/CeO2‐10, and formed highly dispersed Cu clusters (~2.5 nm) on partially reduced CuCeO2 solid solution with abundant of oxygen vacancies upon reduction. The Cu and oxygen vacancies facilitates the activation of H2 and CO2, respectively, resulting in lowered H2 and CO2 reaction orders. As a result, the synergy between the two components enhanced the overall RWGS activity with lowered activation energy. Moreover, the optimal catalyst is very stable in 24h stability test without detectable agglomeration of Cu clusters.
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