催化作用
制氢
甲醇
蒸汽重整
脱氢
一氧化碳
氢
密度泛函理论
工业催化剂
材料科学
化学工程
吉布斯自由能
吸附
化学
无机化学
选择性
碳纤维
合成气
金属
氢燃料
纳米颗粒
过渡金属
作者
Minyi Lu,Yushen Liu,Fan Yang,Yuxin Ge,Xudong Shi,Yongqi Mao,Xinyuan Song,Zejian Li,Jiajin Li,Yuxiang Lyu,Guimei Liu,Zhuoyu Zheng,Yuan Yuan,Junwei Liao,Xitang Qian,Minhua Shao,Tiejun Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-10-29
卷期号:15 (21): 18782-18793
被引量:5
标识
DOI:10.1021/acscatal.5c04297
摘要
Ensuring safer and more satisfactory hydrogen (H2) production from aqueous-phase reforming of methanol (APRM) is crucial for automotive, marine, and aerospace applications. However, nonprecious metal catalysts face challenges in realizing efficient methanol (CH3OH) dehydrogenation and effective carbon monoxide (CO) suppression for APRM without a strong base. In this work, we synthesized Ga2O3-modified Cu–ZnO catalysts with carbon encapsulation, leading to a uniform Cu dispersion. The optimized 12 wt % GCZ-2.0-C450 catalyst exhibits good performance over a wide temperature range (130–210 °C). It achieves a high H2 production rate of 101.2 μmol/gcat/s and low CO selectivity (0.07%) at 210 °C with long-term stability, surpassing the reported Cu- and Pt-based catalysts in APRM. Density functional theory calculations indicate that the Ga2O3 introduction significantly reduces the Gibbs energy of the rate-determining step of *CH3O + *H → *CH2O + *H2, dropping from 1.25 to 0.60 eV. Meanwhile, the adsorption energy of the generated *H2 decreases from −2.92 to −0.13 eV, which facilitates the release of gaseous H2.
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