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用于高效稳定水分解的双活性位点介导的铱单原子掺杂钌氧化物催化剂

Dual active site-mediated Ir single-atom-doped RuO catalysts for highly efficient and stable water splitting.

作者信息

Tao Zhenhua, Lv Ning, Zhao Hongyu, Luo Xu, Li Zilan, Yu Jun, Chen Lei, Liu Xupo, Mu Shichun

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology Wuhan 430070 China

School of Materials Science and Engineering, Henan Normal University Xinxiang Henan 453007 P. R. China.

出版信息

Chem Sci. 2024 Sep 13;15(40):16796-803. doi: 10.1039/d4sc04909h.

Abstract

The electronic structure modulation through heterogeneous single-atom doping is an effective strategy to improve electrocatalysis performance of catalysts. Here, Ir single-atom doped RuO (Ir/RuO) is constructed by substituting Ru sites with mono-disperse Ir atoms in RuO crystals. The Ir/RuO-850 catalyst shows excellent activity for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline media, with overpotentials of only 37 and 234 mV respectively, at a current density of 10 mA cm, lower than that of commercial Pt/C (39 mV-HER) and RuO (295 mV-OER). Notably, no significant degradation occurs during the 1000 h HER stability test at 500 mA cm. Furthermore, Ir/RuO-850 also demonstrates superior catalytic activity and stability in acidic media. Theoretical calculations show that the interaction between Ir and RuO modulates the electronic structure of both Ru and Ir sites, resulting in the lowest reaction energy barriers of Ru and Ir sites for the HER and OER, respectively, which thermodynamically explains the enhancement of the catalytic activity. Besides, the introduction of Ir atoms also enhances the demetallation energy of Ru atoms and strengthens the structural stability of the crystal, leading to the improved stability of the catalyst. This work provides an effective strategy for construction of high-performing catalysts by precisely controlling the electronic structure and active sites of polymetal atoms.

摘要

通过异质单原子掺杂进行电子结构调制是提高催化剂电催化性能的有效策略。在此,通过用单分散的Ir原子取代RuO晶体中的Ru位点,构建了Ir单原子掺杂的RuO(Ir/RuO)。Ir/RuO-850催化剂在碱性介质中对析氢反应(HER)和析氧反应(OER)表现出优异的活性,在电流密度为10 mA cm时,过电位分别仅为37和234 mV,低于商业Pt/C(39 mV-HER)和RuO(295 mV-OER)。值得注意的是,在500 mA cm的1000 h HER稳定性测试期间没有发生明显降解。此外,Ir/RuO-850在酸性介质中也表现出优异的催化活性和稳定性。理论计算表明,Ir与RuO之间的相互作用调制了Ru和Ir位点的电子结构,分别导致Ru和Ir位点对HER和OER的最低反应能垒,这从热力学上解释了催化活性的增强。此外,Ir原子的引入还提高了Ru原子的脱金属能并增强了晶体的结构稳定性,从而提高了催化剂的稳定性。这项工作为通过精确控制多金属原子的电子结构和活性位点来构建高性能催化剂提供了一种有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22db/11483853/b304f9ea27b9/d4sc04909h-f1.jpg

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