Ultrasonically Activated Liquid Metal Catalysts in Water for Enhanced Hydrogenation Efficiency

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY ACS Applied Materials & Interfaces Pub Date : 2025-01-17 DOI:10.1021/acsami.4c19936
Nichayanan Manyuan, Naoya Tanimoto, Kousuke Ueda, Ken Yamamoto, Tomoharu Tokunaga, Masaki Nishio, Tetsu Yonezawa, Hideya Kawasaki
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Abstract

Hydride (H) species on oxides have been extensively studied over the past few decades because of their critical role in various catalytic processes. Their syntheses require high temperatures and the presence of hydrogen, which involves complex equipment, high energy costs, and strict safety protocols. Hydride species tend to decompose in the presence of atmospheric oxygen and water, which reduces their catalytic activities. These challenges highlight the need for further research to improve the stability and efficiency of catalytic processes and develop safer and cost-effective synthesis methods. This paper introduces an ultrasonic fabrication method for gallium hydride species on liquid metal (LM) nanoparticles (Ga–H@LM NPs) in water and describes the evaluation of their catalytic properties. The Ga–H@LM NPs were synthesized by dispersing liquid metals of eutectic gallium–indium in water using a two-step ultrasonication process in an ice bath. The presence of Ga–H species was confirmed by Fourier-transform infrared spectroscopy. The Ga–H@LM NPs demonstrated the rapid catalytic hydrogenation of 4-nitrophenol and reductive degradation of azo dyes within minutes without the need for external reducing agents like NaBH4. The proposed mechanism involves high-energy ultrasonic cavitation at the interface between LM NPs and water, which promotes the formation of H2 from water and its activation to form Ga–H on particles surface during ultrasonication. This study has significant implications for advancing the field of catalysis because it provides a novel and efficient catalytic method for the synthesis of stable hydride species on gallium oxides.

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超声活化液体金属催化剂提高水中加氢效率
氧化物上的氢化物(H -)由于在各种催化过程中起着关键作用,在过去的几十年中得到了广泛的研究。它们的合成需要高温和氢气的存在,这涉及复杂的设备,高能源成本和严格的安全协议。氢化物在大气中氧气和水的存在下容易分解,从而降低了它们的催化活性。这些挑战突出表明需要进一步研究以提高催化过程的稳定性和效率,并开发更安全、更具成本效益的合成方法。本文介绍了一种在水中制备氢化镓纳米粒子(Ga - H@LM NPs)的超声方法,并对其催化性能进行了评价。将共晶镓铟液态金属分散在冰浴中,采用两步超声法合成了Ga - H@LM纳米粒子。傅里叶变换红外光谱证实了Ga-H的存在。Ga - H@LM NPs在不需要NaBH4等外部还原剂的情况下,可以在几分钟内快速催化4-硝基苯酚的加氢和偶氮染料的还原降解。本文提出的机理是在LM NPs与水的界面处产生高能超声空化,在超声作用下促进水生成H2并在颗粒表面活化生成Ga-H。该研究为在氧化镓上合成稳定的氢化物提供了一种新的、高效的催化方法,对催化领域的发展具有重要意义。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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