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用于选择性太阳能驱动CO加氢的二氧化钛负载的Ni P/Ni催化剂。

Titania-Supported Ni P/Ni Catalysts for Selective Solar-Driven CO Hydrogenation.

作者信息

Li Zhenhua, Zhang Xin, Liu Jinjia, Shi Run, Waterhouse Geoffrey I N, Wen Xiao-Dong, Zhang Tierui

机构信息

Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Adv Mater. 2021 Sep;33(36):e2103248. doi: 10.1002/adma.202103248. Epub 2021 Jul 24.

Abstract

Solar-driven Fischer-Tropsch synthesis (FTS) holds great potential for the sustainable production of fuels from syngas and solar energy. However, the selectivity toward multi-carbon products (C ) is often hampered by the difficulty in the regulation of transition metals acting as both light absorption units and active sites. Herein, a partial phosphidation strategy to prepare titania supported Ni P/Ni catalysts for photothermal FTS is demonstrated. Under Xenon lamp or concentrated sunlight irradiation, the optimized catalyst shows a C selectivity of 70% at a CO conversion of >20%. Conversely, nickel metal in the absence of Ni P delivers negligible C products (≈1%) with methane being the major product (>90%). Structural characterization and density functional theory calculation reveal that the partial phosphidation allows exposed metallic Ni to be active for CO adsorption and activation, while the existence of Ni P/Ni interface is responsible to inhibit CO methanation and promote C-C coupling of adsorbed *CH intermediates. This work introduces a novel phosphidation strategy for nickel-based photothermal catalysts in efficiently harnessing solar energy, and regulating the reaction pathways for CO hydrogenation to deliver high value products.

摘要

太阳能驱动的费托合成(FTS)在利用合成气和太阳能可持续生产燃料方面具有巨大潜力。然而,由于难以调控兼具光吸收单元和活性位点功能的过渡金属,多碳产物(C)的选择性常常受到阻碍。在此,展示了一种用于制备用于光热FTS的二氧化钛负载的NiP/Ni催化剂的部分磷化策略。在氙灯或聚光太阳光照射下,优化后的催化剂在CO转化率>20%时表现出70%的C选择性。相反,不存在NiP的镍金属产生的C产物可忽略不计(≈1%),甲烷是主要产物(>90%)。结构表征和密度泛函理论计算表明,部分磷化使暴露的金属Ni对CO吸附和活化具有活性,而NiP/Ni界面的存在负责抑制CO甲烷化并促进吸附的*CH中间体的C-C偶联。这项工作为镍基光热催化剂引入了一种新颖的磷化策略,可有效利用太阳能,并调控CO加氢反应路径以生成高价值产物。

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