甲烷化
催化作用
钴
选择性
材料科学
格式化
化学工程
碳纤维
甲烷
纳米颗粒
可再生能源
稳健性(进化)
热的
替代天然气
热导率
无机化学
金属有机骨架
增强碳-碳
过渡金属
化学
金属
能量载体
纳米技术
活化能
热膨胀
作者
Jingzhong Qin,Shuaishuai Yin,Caizhi Yu,Y R Tao,Jiayu Mu,Menglin Wang,Jiahua Luo,Li Zhang,Yi Zhou,Ziyi Yan,Li Zhang,Yunqian Dai,Wenlong Wu,Hongliang Li,Jie Zeng
摘要
ABSTRACT The development of robust catalysts for CO 2 methanation under intermittent operating conditions is key to harnessing renewable energy sources such as wind and solar. However, this pursuit faces two major obstacles. The heating‐cooling cycles induce prolonged thermal stress, resulting in catalyst deactivation. Moreover, the temperature‐sensitive selectivity hampers the ability to maintain high methane yield, leading to undesired by‐products. Herein, we report cobalt nanoparticles confined within carbon matrices, which achieved 82.3% CO 2 conversion and > 99% CH 4 selectivity over multiple heating‐cooling cycles toward intermittent CO 2 methanation. The catalyst robustness arises from the low coefficient of thermal expansion and high thermal conductivity of the carbon matrix, which effectively mitigates thermal stress during temperature fluctuations. Mechanistic studies confirm that the reaction proceeds via a formate pathway, which contributes to the high CH 4 selectivity across a wide temperature range. These insights provide a design framework for developing robust catalysts, advancing CO 2 methanation performance, and the efficient use of fluctuating renewable energy sources.
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