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Copper doped ceria porous nanostructures towards a highly efficient bifunctional catalyst for carbon monoxide and nitric oxide elimination

机译:铜掺杂的二氧化铈多孔纳米结构用于消除一氧化碳和一氧化氮的高效双功能催化剂

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摘要

Copper doped ceria porous nanostructures with a tunable BET surface area were prepared using an efficient and general metal–organic-framework-driven, self-template route. The XRD, SEM and TEM results indicate that Cu2+ was successfully substituted into the CeO2 lattice and well dispersed in the CeO2:Cu2+ nanocrystals. The CeO2:Cu2+ nanocrystals exhibit a superior bifunctional catalytic performance for CO oxidation and selective catalytic reduction of NO. Interestingly, CO oxidation reactivity over the CeO2:Cu2+ nanocrystals was found to be dependent on the Cu2+ dopants and BET surface area. By tuning the content of Cu2+ and BET surface area through choosing different organic ligands, the 100% conversion temperature of CO over CeO2:Cu2+ nanocrystals obtained from thermolysis of CeCu–BPDC nanocrystals can be decreased to 110 °C. The porous nanomaterials show a high CO conversion rate without any loss in activity even after five cycles. Furthermore, the activity of the catalysts for NO reduction increased with the increase of BET surface, which is in accordance with the results of CO oxidation.
机译:使用有效且通用的金属-有机框架驱动的自模板路线制备了具有可调BET表面积的掺杂铜的氧化铈多孔纳米结构。 XRD,SEM和TEM结果表明,Cu 2 + 已被成功取代到CeO2晶格中,并很好地分散在CeO2:Cu 2 + 纳米晶体中。 CeO2:Cu 2 + 纳米晶体在CO氧化和NO的选择性催化还原方面表现出优异的双功能催化性能。有趣的是,发现CeO2:Cu 2 + 纳米晶体上的CO氧化反应性取决于Cu 2 + 掺杂剂和BET表面积。通过选择不同的有机配体来调节Cu 2 + 的含量和BET表面积,CO转化为CeO2:Cu 2 + 纳米晶体的100%转化温度是通过热解得到的。 CeCu–BPDC纳米晶体可以降低到110°C。多孔纳米材料即使在五个循环后仍显示出高的CO转化率,而没有任何活性损失。此外,催化剂的NO还原活性随BET表面的增加而增加,这与CO氧化的结果一致。

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