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二维亚稳相氧化铪引发氢溢流以促进产氢。

2D Metastable-Phase Hafnium Oxide Triggers Hydrogen Spillover for Boosting Hydrogen Production.

作者信息

Wang Qun, Chen Jinxin, Chen Shiya, Zhou Dingyanyan, Du Yutong, Ji Yujin, Xiong Yutian, Ke Jia, Zhu Wenxiang, Wang Yue, Gao Dongdong, Huang Wei-Hsiang, Pao Chih-Wen, Sun Yang, Li Youyong, Shao Mingwang, Hu Zhiwei, Huang Xiaoqing, Shao Qi

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, Jiangsu, 215123, China.

Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, Jiangsu, 215123, China.

出版信息

Adv Mater. 2025 Apr;37(13):e2415978. doi: 10.1002/adma.202415978. Epub 2025 Feb 27.

Abstract

Hydrogen (H) manipulation plays a significantly important role in many important applications, in which the occurrence of hydrogen spillover generally shows substrate-dependent behavior. It therefore remains an open question about how to trigger the hydrogen spillover on the substrates that are generally hydrogen spillover forbidden. Here a new metastable-phase 2D edge-sharing oxide: six-hexagonal phase-hafnium oxide (Hex-HfO, space group: P6mc (186)) with the coordination number of six is demonstrated, which serves as an ideal platform for activating efficient hydrogen spillover after loading Ru nanoclusters (Ru/Hex-HfO). For a stark comparison, the hydrogen spillover is strongly forbidden when using stable monoclinic phase HfO (M-HfO, space group: P2/c (14), coordination number: seven) as the substrate. When applied in an acidic hydrogen evolution reaction (HER), Ru/Hex-HfO exhibits a low overpotential of 8 mV at 10 mA cm and a high Ru utilization activity of 14.37 A mg at 30 mV. Detailed mechanism reveals the positive H adsorption free energy on Hex-HfO, indicating that H is more likely to spillover on Hex-HfO. Furthermore, the strong interaction between Ru and Hex-HfO optimizes the desorption of hydrogen intermediate, thus facilitating the surface H spillover. The discovery provides new guidance for developing metastable-phase oxide substrates for advanced catalysis.

摘要

氢(H)调控在许多重要应用中起着至关重要的作用,其中氢溢流的发生通常表现出底物依赖性行为。因此,如何在通常禁止氢溢流的底物上引发氢溢流仍是一个悬而未决的问题。在此,展示了一种新的亚稳相二维边共享氧化物:六方相氧化铪(Hex-HfO,空间群:P6mc(186)),其配位数为6,在负载Ru纳米团簇(Ru/Hex-HfO)后,它作为激活高效氢溢流的理想平台。为了进行鲜明对比,当使用稳定的单斜相HfO(M-HfO,空间群:P2/c(14),配位数:7)作为底物时,氢溢流被强烈禁止。当应用于酸性析氢反应(HER)时,Ru/Hex-HfO在10 mA cm下表现出8 mV的低过电位,在30 mV下具有14.37 A mg的高Ru利用活性。详细的机理揭示了Hex-HfO上正的H吸附自由能,表明H更有可能在Hex-HfO上溢流。此外,Ru与Hex-HfO之间的强相互作用优化了氢中间体的脱附,从而促进了表面H溢流。这一发现为开发用于先进催化的亚稳相氧化物底物提供了新的指导。

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