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氢溢流增强了富含界面的金属负载MoO上的碱性氢电催化作用。

Hydrogen spillover enhances alkaline hydrogen electrocatalysis on interface-rich metallic Pt-supported MoO.

作者信息

Samanta Rajib, Manna Biplab Kumar, Trivedi Ravi, Chakraborty Brahmananda, Barman Sudip

机构信息

School of Chemical Sciences, National Institute of Science Education and Research (NISER), HBNI Bhubaneswar Orissa 752050 India

Homi Bhabha National Institute, Training School Complex Anushakti Nagar Mumbai 400094 India.

出版信息

Chem Sci. 2023 Dec 8;15(1):364-378. doi: 10.1039/d3sc04126c. eCollection 2023 Dec 20.

Abstract

Efficient and cost-effective electrocatalysts for the hydrogen oxidation/evolution reaction (HOR/HER) are essential for commercializing alkaline fuel cells and electrolyzers. The sluggish HER/HOR reaction kinetics in base is the key issue that requires resolution so that commercialization may proceed. It is also quite challenging to decrease the noble metal loading without sacrificing performance. Herein, we report improved HER/HOR activity as a result of hydrogen spillover on platinum-supported MoO (Pt/MoO-CN-400) with a Pt loading of 20%. The catalyst exhibited a decreased over-potential of 66.8 mV to reach 10 mA cm current density with a Tafel slope of 41.2 mV dec for the HER in base. The Pt/MoO-CN-400 also exhibited satisfactory HOR activity in base. The mass-specific exchange current density of Pt/MoO-CN-400 and commercial Pt/C are 505.7 and 245 mA mg, respectively. The experimental results suggest that the hydrogen binding energy (HBE) is the key descriptor for the HER/HOR. We also demonstrated that the enhanced HER/HOR performance was due to the hydrogen spillover from Pt to MoO sites that enhanced the Volmer/Heyrovsky process, which led to high HER/HOR activity and was supported by the experimental and theoretical investigations. The work function value of Pt [ = 5.39 eV) is less than that of β-MoO (011) [ = 7.09 eV], which revealed the charge transfer from Pt to the β-MoO (011) surface. This suggested the feasibility of hydrogen spillover, and was further confirmed by the relative hydrogen adsorption energy [Δ] at different sites. Based on these findings, we propose that the HO or H dissociation takes place on Pt and interfaces to form Pt-H or (Pt/MoO)-H, and some of the H shifted to MoO sites through hydrogen spillover. Then, H at the Pt and interface, and MoO sites reacted with HO and HO to form H or HO molecules, thereby boosting the HER/HOR activity. This work may provide valuable information for the development of hydrogen-spillover-based electrocatalysts for use in various renewable energy devices.

摘要

用于氢氧化/析氢反应(HOR/HER)的高效且具有成本效益的电催化剂对于碱性燃料电池和电解槽的商业化至关重要。碱性条件下缓慢的HER/HOR反应动力学是实现商业化必须解决的关键问题。在不牺牲性能的情况下降低贵金属负载量也颇具挑战性。在此,我们报道了由于氢溢流作用,在铂负载量为20%的负载型MoO(Pt/MoO-CN-400)上HER/HOR活性得到了提高。该催化剂在碱性条件下析氢时,达到10 mA cm电流密度的过电位降低了66.8 mV,塔菲尔斜率为41.2 mV dec。Pt/MoO-CN-400在碱性条件下也表现出令人满意的析氢活性。Pt/MoO-CN-400和商业Pt/C的质量比交换电流密度分别为505.7和245 mA mg。实验结果表明,氢结合能(HBE)是HER/HOR的关键描述符。我们还证明,增强的HER/HOR性能归因于氢从Pt溢流到MoO位点,从而增强了Volmer/Heyrovsky过程,这导致了高HER/HOR活性,并且得到了实验和理论研究的支持。Pt的功函数值(= 5.39 eV)小于β-MoO(011)的功函数值(= 7.09 eV),这表明电荷从Pt转移到β-MoO(011)表面。这表明了氢溢流的可行性,并通过不同位点的相对氢吸附能[Δ]进一步得到证实。基于这些发现,我们提出HO或H在Pt及其界面上解离形成Pt-H或(Pt/MoO)-H,并且一些H通过氢溢流转移到MoO位点。然后,Pt和界面处以及MoO位点的H与HO和HO反应形成H或HO分子,从而提高了HER/HOR活性。这项工作可能为开发用于各种可再生能源装置的基于氢溢流的电催化剂提供有价值的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e53e/10732227/715a0bb24423/d3sc04126c-f1.jpg

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