脱氢
催化作用
镍
沸石
材料科学
纳米颗粒
金属
化学工程
纳米技术
化学
冶金
有机化学
工程类
作者
Huixin Wu,Hai Wang,Yating Lv,Yuexin Wu,Yike Wang,Qingsong Luo,Hui Yu,Lujie Liu,Mengting Zhang,Kunming Hou,Lina Li,Jianrong Zeng,Weili Dai,Li Wang,Feng‐Shou Xiao
标识
DOI:10.1002/anie.202420306
摘要
Each step in the catalyst synthesis process plays an important role in tuning the catalyst structures. For zeolite‐supported nickel catalysts, we found the conventional calcination‐reduction method typically leads to the formation of large nickel particles, but a pre‐aging in hydrogen or nitrogen at a low temperature prior to final reduction can result in ultra‐small nickel nanoparticles in a metallic state. This pre‐aging treatment facilitates the interaction between Ni2+ cations and silanol nests on zeolite before the decomposition of the metal salt, leading to the formation of nanoparticles with an average diameter of ~1.2 nm. In contrast, the pre‐calcination in oxygen caused the Ni2+ aggregation before the decomposition of the metal salt precursor, yielding nickel nanoparticles larger than 5 nm. Given the structure sensitivity of nickel in cyclohexane dehydrogenation for hydrogen production, the ultra‐small nickel nanoparticles exhibited significantly enhanced activity and durability compared to previous nickel catalysts.
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