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Triggering comprehensive enhancement in oxygen evolution reaction by using newly created solvent

机译:通过使用新创建的溶剂引发析氧反应全面提升

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摘要

Theoretical calculations indicate that the properties of confined liquid water, or liquid water at surfaces, are dramatically different from those of liquid bulk water. Here we present an experimentally innovative strategy on comprehensively efficient oxygen evolution reaction (OER) utilizing plasmon-induced activated water, creating from hot electron decay at resonantly illuminated Au nanoparticles (NPs). Compared to conventional deionized (DI) water, the created water owns intrinsically reduced hydrogen-bonded structure and a higher chemical potential. The created water takes an advantage in OER because the corresponding activation energy can be effectively reduced by itself. Compared to DI water-based solutions, the OER efficiencies at Pt electrodes increased by 69.3%, 21.1% and 14.5% in created water-based acidic, neutral and alkaline electrolyte solutions, respectively. The created water was also effective for OERs in photoelectrochemically catalytic and in inert systems. In addition, the efficiency of OER increased by 47.5% in created water-based alkaline electrolyte solution prepared in situ on a roughened Au electrode. These results suggest that the created water has emerged as an innovative activator in comprehensively effective OERs.
机译:理论计算表明,狭窄的液体水或表面的液态水的性质与液体散热的显着不同。在这里,我们提出了一种关于综合有效的氧气进化反应(OER)的实验创新策略,利用等离子体诱导的活性水,从谐振照射的Au纳米颗粒(NPS)以热电子衰减产生。与常规的去离子(DI)水相比,所产生的水使本质上减少的氢键结构和更高的化学势。所产生的水在OER中具有优势,因为相应的激活能量本身可以有效地减少。与迪水性溶液相比,Pt电极的oer效率分别在产生的水基酸性,中性和碱性电解质溶液中增加了69.3%,21.1%和14.5%。由于光电化学催化剂和惰性系统中的OERS,所产生的水也有效。此外,在粗糙的Au电极上原位制备的产生的水基碱性电解质溶液中,OER的效率增加了47.5%。这些结果表明,创造的水作为全面有效的OERS中的创新激活因子。

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