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稳定的 Ni-Mo 纳米催化剂在单晶 MgO 上进行甲烷干重整。

Dry reforming of methane by stable Ni-Mo nanocatalysts on single-crystalline MgO.

机构信息

Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141 Korea.

Graduate School of EEWS, KAIST, Daejeon, 34141 Korea.

出版信息

Science. 2020 Feb 14;367(6479):777-781. doi: 10.1126/science.aav2412.

Abstract

Large-scale carbon fixation requires high-volume chemicals production from carbon dioxide. Dry reforming of methane could provide an economically feasible route if coke- and sintering-resistant catalysts were developed. Here, we report a molybdenum-doped nickel nanocatalyst that is stabilized at the edges of a single-crystalline magnesium oxide (MgO) support and show quantitative production of synthesis gas from dry reforming of methane. The catalyst runs more than 850 hours of continuous operation under 60 liters per unit mass of catalyst per hour reactive gas flow with no detectable coking. Synchrotron studies also show no sintering and reveal that during activation, 2.9 nanometers as synthesized crystallites move to combine into stable 17-nanometer grains at the edges of MgO crystals above the Tammann temperature. Our findings enable an industrially and economically viable path for carbon reclamation, and the "Nanocatalysts On Single Crystal Edges" technique could lead to stable catalyst designs for many challenging reactions.

摘要

大规模碳固定需要从二氧化碳中大量生产化学品。如果开发出抗积碳和烧结的催化剂,甲烷的干重整可能提供一种经济可行的途径。在这里,我们报告了一种在单晶氧化镁(MgO)载体边缘稳定的掺杂钼的镍纳米催化剂,并展示了从甲烷的干重整中定量生产合成气。该催化剂在每小时每单位质量催化剂 60 升反应气体流量下连续运行超过 850 小时,没有可检测到的积碳。同步辐射研究还表明没有烧结,并揭示了在活化过程中,2.9 纳米的合成纳米晶体在 Tammann 温度以上迁移到 MgO 晶体边缘结合成稳定的 17 纳米晶粒。我们的发现为碳回收提供了一条具有工业和经济可行性的途径,而“单晶边缘上的纳米催化剂”技术可能为许多具有挑战性的反应带来稳定的催化剂设计。

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