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低温下将贵金属纳米颗粒热解为富电子磷配位的贵金属单原子

Thermolysis of Noble Metal Nanoparticles into Electron-Rich Phosphorus-Coordinated Noble Metal Single Atoms at Low Temperature.

作者信息

Zhou Peng, Li Ning, Chao Yuguang, Zhang Weiyu, Lv Fan, Wang Kai, Yang Wenxiu, Gao Peng, Guo Shaojun

机构信息

Department of Materials Science and Engineering, Peking University, Beijing, 100871, China.

Beijing Innovation Center for Engineering Science and Advanced Technology, Peking University, Beijing, 100871, China.

出版信息

Angew Chem Int Ed Engl. 2019 Oct 1;58(40):14184-14188. doi: 10.1002/anie.201908351. Epub 2019 Aug 28.

DOI:10.1002/anie.201908351
PMID:31365167
Abstract

Noble metal single atoms coordinated with highly electronegative atoms, especially N and O, often suffer from an electron-deficient state or poor stability, greatly limiting their wide application in the field of catalysis. Herein we demonstrate a new PH -promoted strategy for the effective transformation of noble metal nanoparticles (MNPs, M=Ru, Rh, Pd) at a low temperature (400 °C) into a class of thermally stabilized phosphorus-coordinated metal single atoms (MPSAs) on g-C N nanosheets via the strong Lewis acid-base interaction between PH and the noble metal. Experimental work along with theoretical simulations confirm that the obtained Pd single atoms supported on g-C N nanosheets exist in the form of PdP with a novel electron-rich feature, conceptionally different from the well-known single atoms with an electron-deficient state. As a result of this new electronic property, PdP -loaded g-C N nanosheets exhibit 4 times higher photocatalytic H production activity than the state-of-art N-coordinated PdSAs supported on g-C N nanosheets. This enhanced photocatalytic activity of phosphorus-coordinated metal single atoms with an electron-rich state was quite general, and also observed for other active noble metal single atom catalysts, such as Ru and Rh.

摘要

与高电负性原子(尤其是N和O)配位的贵金属单原子,常常处于缺电子状态或稳定性较差,这极大地限制了它们在催化领域的广泛应用。在此,我们展示了一种新的PH促进策略,通过PH与贵金属之间强烈的路易斯酸碱相互作用,在低温(400 °C)下将贵金属纳米颗粒(MNPs,M = Ru、Rh、Pd)有效地转化为一类负载于g-CN纳米片上的热稳定的磷配位金属单原子(MPSAs)。实验工作以及理论模拟证实,负载于g-CN纳米片上的所得Pd单原子以具有新颖富电子特征的PdP形式存在,这在概念上不同于众所周知的缺电子状态的单原子。由于这种新的电子性质,负载PdP的g-CN纳米片表现出比负载于g-CN纳米片上的最先进的N配位PdSAs高4倍的光催化产氢活性。这种具有富电子状态的磷配位金属单原子的增强光催化活性具有普遍性,在其他活性贵金属单原子催化剂(如Ru和Rh)中也观察到了这一现象。

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