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纳米颗粒作为可持续丙烯环氧化中毒金单原子催化剂的解毒剂。

Nanoparticles as an antidote for poisoned gold single-atom catalysts in sustainable propylene epoxidation.

作者信息

Wang Qianhong, Sang Keng, Liu Changwei, Zhang Zhihua, Chen Wenyao, Ji Te, Li Lina, Lian Cheng, Qian Gang, Zhang Jing, Zhou Xinggui, Yuan Weikang, Duan Xuezhi

机构信息

State Key Laboratory of Chemical Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, China.

Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Shanghai, 201210, China.

出版信息

Nat Commun. 2024 Apr 16;15(1):3249. doi: 10.1038/s41467-024-47538-4.

DOI:10.1038/s41467-024-47538-4
PMID:38627484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11021464/
Abstract

The development of sustainable and anti-poisoning single-atom catalysts (SACs) is essential for advancing their research from laboratory to industry. Here, we present a proof-of-concept study on the poisoning of Au SACs, and the antidote of Au nanoparticles (NPs), with trace addition shown to reinforce and sustain propylene epoxidation. Multiple characterizations, kinetics investigations, and multiscale simulations reveal that Au SACs display remarkable epoxidation activity at a low propylene coverage, but become poisoned at higher coverages. Interestingly, Au NPs can synergistically cooperate with Au SACs by providing distinct active sites required for H/O and CH activations, as well as hydroperoxyl radical to restore poisoned SACs. The difference in reaction order between CH and H (n-n) is identified as the descriptor for establishing the volcano curves, which can be fine-tuned by the intimacy and composition of SACs and NPs to achieve a rate-matching scenario for the formation, transfer, and consumption of hydroperoxyl. Consequently, only trace addition of Au NPs antidote (0.3% ratio of SACs) stimulates significant improvements in propylene oxide formation rate, selectivity, and H efficiency compared to SACs alone, offering a 56-fold, 3-fold, and 22-fold increase, respectively, whose performances can be maintained for 150 h.

摘要

开发可持续且抗中毒的单原子催化剂(SACs)对于推动其从实验室研究走向工业应用至关重要。在此,我们展示了一项关于金单原子催化剂中毒以及金纳米颗粒(NPs)解毒作用的概念验证研究,结果表明痕量添加能增强并维持环氧丙烷的氧化反应。多种表征、动力学研究以及多尺度模拟表明,金单原子催化剂在低丙烯覆盖率下表现出显著的环氧化活性,但在较高覆盖率下会中毒。有趣的是,金纳米颗粒可以通过提供氢/氧和碳氢活化所需的独特活性位点以及氢过氧自由基来与金单原子催化剂协同合作,从而恢复中毒的单原子催化剂。碳氢和氢反应级数的差异(n-n)被确定为建立火山曲线的描述符,可通过单原子催化剂和纳米颗粒的紧密程度及组成进行微调,以实现氢过氧自由基形成、转移和消耗的速率匹配情况。因此,与单独的单原子催化剂相比(0.3%的单原子催化剂与纳米颗粒比例),仅痕量添加金纳米颗粒解毒剂就能显著提高环氧丙烷的生成速率、选择性和氢效率,分别提高了56倍、3倍和22倍,其性能可维持150小时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/574f4c53f664/41467_2024_47538_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/143bc7417ac5/41467_2024_47538_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/3e8abd649c2f/41467_2024_47538_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/7120d87db256/41467_2024_47538_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/ea4fa8a9d5de/41467_2024_47538_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/6131f2ad338a/41467_2024_47538_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/574f4c53f664/41467_2024_47538_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/143bc7417ac5/41467_2024_47538_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/3e8abd649c2f/41467_2024_47538_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/7120d87db256/41467_2024_47538_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/ea4fa8a9d5de/41467_2024_47538_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/6131f2ad338a/41467_2024_47538_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f95/11021464/574f4c53f664/41467_2024_47538_Fig6_HTML.jpg

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