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首页> 外文期刊>Materials Chemistry Frontiers >In situ construction of 1D/2D ZnO/graphdiyne oxide heterostructures for enhanced photocatalytic reduction in a gas phase
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In situ construction of 1D/2D ZnO/graphdiyne oxide heterostructures for enhanced photocatalytic reduction in a gas phase

机译:原位构建一维/二维ZnO/氧化石墨炔异质结,增强气相光催化还原

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摘要

In this study, a 1D/2D ZnO nanofiber/graphdiyne oxide heterojunction was designed for photocatalytic CO2 reduction, and the difference between graphdiyne and graphdiyne oxide was investigated as co-catalysts. The ZGDO heterostructure has strong reactant adsorption capacity due to the enlarged specific surface area and abundant hydrophilic oxygen-containing functional groups. DFT calculations, EPR, and in situ XPS further verified the S-scheme charge transfer mechanism in ZGDO. In contrast, the abilities of GD to adsorb CO2 and enhance light absorption are not as good as those of GDO, and the band structure of GD is not conducive to the formation of a favorable electric field drive at the interface with ZnO. The CO yield of ZGDO with only 3% GDO was up to 34.9 mmol h~(-1) g~(-1) in the gas-phase photocatalytic reduction of CO2, which was 4.4, 24, and 1.5 times that of ZnO, GDO, and ZnO/GD, respectively. This work opens new possibilities for the application of new non-metallic photocatalysts in the photoreduction of CO2.
机译:在这项研究中,1 d / 2 d氧化锌纳米纤维/ graphdiyne氧化物异质结的设计光催化二氧化碳减少,差异graphdiyne和氧化graphdiyne之间作为co-catalysts调查。异质结构具有强烈的反应物吸附由于大比表面的能力面积和亲水性含氧丰富官能团。原地XPS进一步验证了S-scheme电荷在ZGDO转移机制。GD吸附二氧化碳的能力,提高光吸收是不如GDO,和GD不利于的能带结构形成良好的电场驱动接口与氧化锌。只有3% GDO 34.9更易与h ~ (1) g ~ (1)的气相光催化还原二氧化碳,这是4.4,24岁,和氧化锌的1.5倍,分别GDO和氧化锌/ GD。新的应用程序的新可能性非金属催化剂的光致还原作用的二氧化碳。

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