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  • 教师姓名: 郭洋
  • 性别: 男
  • 职称: 副教授
  • 博士生导师: 是
  • 硕士生导师: 是
  • 学历: 博士研究生毕业
  • 学位: 博士
  • 所在单位: 能源与动力工程学院
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    创新港校区:1号巨构5187

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Tailored Interfaces Promoting Photo-Activation of Molecular Enclosed CO2 on MOF-Derived Ni/CeZrO2 for Photothermal Synergistic Dry Reforming of Methane

发布时间:2026-09-18
点击次数:
发布时间:
2026-09-18
论文名称:
Tailored Interfaces Promoting Photo-Activation of Molecular Enclosed CO2 on MOF-Derived Ni/CeZrO2 for Photothermal Synergistic Dry Reforming of Methane
发表刊物:
Chemical Engineering Journal
摘要:
Photothermal synergistic catalysis dry reforming of methane (PTSC-DRM) has attracted considerable interest due to its capability to convert CH4 and CO2 into syngas under mild conditions. The development of high-performance catalysts that efficiently harness both light and heat while resisting carbon deposition remains challenging. In this study, we present a Ni/CeZrO2 catalyst derived from metal-organic frameworks (MOF). Characterization techniques such as TEM confirmed the presence of abundant interface sites, which enhance the metal-support interactions. This configuration facilitates the establishment of a CO2 molecular fence around nickel nanoparticles, thereby increasing reaction rates and mitigating carbon deposition through enhanced CO2 photoactivation. At 650 °C, the conversion rates of CH4 and CO2 reached 63.9 % and 71.1 %, respectively. In situ DRFITS and CO2-TPD characterization, along with theoretical calculations, revealed superior CO2 adsorption at the Ni-O-Zr sites, promoting the formation of carbon-tolerant intermediates (CHxO*) under light irradiation, which are subsequently oxidized by OH* to produce CO and H2. This remarkable light-induced decarbonization mechanism allows the catalyst to effectively suppress carbon deposition and accelerate carbon oxidation. At 600 °C, unlike the severe carbon accumulation observed with Ni/CeO2 during 70 h of online testing, the Ni/CeZrO2 catalyst maintains stable PTSC-DRM activity for over 250 h without significant performance degradation.
合写作者:
Yuhao Liu, Xu Liu, Dan Li, Tengfei Li, Yang Guo(通讯作者)
学科门类:
工学
文献类型:
J
卷号:
512
页面范围:
162499
是否译文:
否
发表时间:
2025-05-15
收录刊物:
SCI