由高熵氧化物衍生的高熵合金:解锁二氧化碳绿色甲醇生产的活性位点

IF 27.4 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Devender Goud, Madhurima Sarkar, Harishankar Kopperi, Amitabha Das, Bitan Ray, Sreelakshmi Vijayaraghavan, Biswarup Pathak, Sebastian C Peter
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引用次数: 0

摘要

为了寻找将二氧化碳转化为增值化学品的新材料,以前的研究主要集中在铜基、氧化铟(In2O3)基和合金或金属间材料上。然而,通过引入高熵基材料将二氧化碳还原为甲醇(CH3OH),提出了一种开创性的方法。该方法具有可扩展性和简单性,可用于大规模生产高熵合金(HEAs)。铁的存在促进了HEA的形成,导致在煅烧过程中产生高熵氧化物(HEO)。通过x射线光电子能谱(XPS)和x射线吸收能谱(XAS)综合分析了HEO和HEA中所有金属的氧化态和配位环境。Fe3O4在HEO结构内的形成是明显的,每种金属都占据了四面体(Td)或八面体(Oh)的位置。生成的HEA具有优异的CO2转化效率和较高的CH3OH选择性。Co, Ni与Fe, Cu和Zn的分离位点以及CuZn对被认为是CO2到CH3OH的活性位点,并进一步通过DFT计算确定。利用原位漫反射红外傅立叶变换光谱(DRIFTS)研究了与单个金属相比,HEA形成时反应机制的改变。最后,生命周期评价(LCA)表明碳负足迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High Entropy Alloy Formation Derived from High Entropy Oxide: Unlocking the Active Sites for Green Methanol Production from CO2

High Entropy Alloy Formation Derived from High Entropy Oxide: Unlocking the Active Sites for Green Methanol Production from CO2

High Entropy Alloy Formation Derived from High Entropy Oxide: Unlocking the Active Sites for Green Methanol Production from CO2

In pursuit of novel materials for CO2 conversion to value-added chemicals, previous research has predominantly focused on copper-based, indium oxide (In2O3)-based, and alloy or intermetallic materials. However, a groundbreaking approach is presented by introducing a high-entropy-based material for CO2 reduction to methanol (CH3OH). This method offers scalability and simplicity, making it feasible for large-scale production of high-entropy-alloys (HEAs). The formation of HEA is facilitated by the presence of Fe, leads to the creation of a high-entropy oxide (HEO) during calcination. Through X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS), comprehensively analyzed the oxidation states and coordination environments of all metals in both HEO and HEA. The formation of Fe3O4 within the HEO structure is evident, with each metal occupying either tetrahedral (Td) or octahedral (Oh) sites. The HEA formed shows exceptional CO2 conversion efficiency and higher CH3OH selectivity. Isolated sites of Co, Ni with Fe, Cu, and Zn, along with CuZn pair, are considered as the active sites for CO2 to CH3OH and further determined by DFT calculations. The altered reaction mechanism upon HEA formation compared to individual metals is investigated using in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Finally, Life-cycle assessment (LCA) indicates the carbon-negative footprint.

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来源期刊
Advanced Materials
Advanced Materials 工程技术-材料科学:综合
CiteScore
43.00
自引率
4.10%
发文量
2182
审稿时长
2 months
期刊介绍: Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.
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