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Ni5Ga3 catalysts for CO2 reduction to methanol: Exploring the role of Ga surface oxidation/reduction on catalytic activity

机译:Ni5Ga3催化剂的CO2还原成甲醇:探索GA表面氧化/减少对催化活性的作用

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摘要

A delta-NisGa(3)/SiO2 catalyst, which is highly active and stable for thermal CO2 hydrogenation to methanol, was investigated to understand its surface dynamics during reaction conditions. The catalyst was prepared, tested and characterized using a multitude of techniques, including ex-situ XRD (X-ray Diffraction), TEM (Transmission Electron Microscopy), H-2-TPR (Temperature Programmed Reduction), CO chemisorption, along with in-situ STEM (Environmental Transmission Electron Microscopy), APXPS (Ambient Pressure X-ray Photoelectron Spectroscopy) and HERFD-XAS (High Energy Resolution Fluorescence Detected X-Ray Absorption Spectroscopy). Upon air exposure Ga migrates from the subsurface region to the surface of the nanoparticles forming a Ga-oxide shell surrounding a metallic core. The oxide shell can be reduced completely only at high temperatures (above 600 degrees C); the temperature of the reducing activation treatment plays a crucial role on the catalytic activity. HERFD-XAS and APXPS measurements show that an amorphous Ga2O3 shell persists during catalysis after low temperature reductions, promoting methanol synthesis.
机译:研究了δ-NISGA(3)/ SiO 2催化剂,其对于热CO 2氢化至甲醇的高活性和稳定性,以在反应条件下了解其表面动力学。使用多种技术制备,测试和表征催化剂,包括ex-situ XRd(X射线衍射),TEM(透射电子显微镜),H-2-TPR(温度编程还原),CO ChemisoItal以及-Situ茎(环境透射电子显微镜),APXPS(环境压力X射线光电子能谱)和HERFD-XA(高能量分辨率荧光检测到的X射线吸收光谱)。在空气暴露时,Ga从地下区域迁移到形成围绕金属芯的Ga氧化物壳的纳米颗粒的表面。氧化物壳可以仅在高温下完全减少(高于600℃);还原活化处理的温度对催化活性起着至关重要的作用。 HERFD-XAS和APXPS测量表明,在低温降低后,无定形GA2O3壳体在催化期间持续,促进甲醇合成。

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