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Synthesis of active, robust and cationic Au25 cluster catalysts on double metal hydroxide by long-term oxidative aging of Au25(SR)18

机译:合成的活跃,健壮和阳离子Au25集群在双金属氢氧化物催化剂长期的氧化老化Au25 (SR) 18

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摘要

Synthesis of an atomically precise Au25 cluster catalyst was attempted by long-term, low-temperature aging of Au25(BaET)18 (BaET-H = 2-(Boc-amino)ethanethiol) on various double metal hydroxide (DMH) supports. X-ray absorption fine structure analysis revealed that bare Au25 clusters with high loading (1 wt%) were successfully generated on the DMH containing Co and Ce (Co3Ce) by oxidative aging in air at 150 °C for >12 h. X-ray absorption near-edge structure and X-ray photoelectron spectroscopies showed that the Au25 clusters on Co3Ce were positively charged. The Au25/Co3Ce catalyst thus synthesized exhibited superior catalytic performance in the aerobic oxidation of benzyl alcohol under ambient conditions (TOF = 1097 h−1 with >97% selectivity to benzoic acid) and high durability owing to a strong anchoring effect. Based on kinetic experiments, we propose that abstraction of hydride from α-carbon of benzyl alkoxide by Au25 is the rate-determining step of benzyl alcohol oxidation by Au25/Co3Ce.
机译:合成的自动精确Au25集群催化剂被长期的尝试,低温老化的Au25 (BaET) 18 (BaET-H =(2) - Boc-amino乙硫醇)在各种双金属氢氧化(DMH)支持。结构分析表明裸Au25集群高加载(1 wt %)成功上生成DMH包含有限公司和Ce (Co3Ce)在空气中氧化衰老,享年150岁°C > 12 h。x射线吸收靠近边缘结构和x射线光电子能谱表明Au25 Co3Ce是集群带正电的。表现出优异的催化合成苄有氧氧化的性能酒精在环境条件下(TOF = 1097 h−1> 97%苯甲酸)和高选择性耐久性由于强烈的锚定效应。基于动力学实验,我们提议抽象的氢化物α碳苄醇盐Au25的速率决定步骤苯甲醇氧化Au25 / Co3Ce。

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