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通过中红外刺激微调界面水来提高金属表面的氧还原活性。

Boosting the oxygen reduction activity on metal surfaces by fine-tuning interfacial water with midinfrared stimulation.

作者信息

Zhang Qilin, Wu Yu, Sun Hao, Zhu Zhongjie, Zhao Hongwei, Yang Jinrong, Wang Jie, Chen Min, Song Sanzhao, Zheng Shiyou, Zhang Dengsong, Yang Hui, Zhu Zhi, Wang Chunlei

机构信息

School of Mathematics Physics and Finance, Anhui Polytechnic University, Wuhu 241000, China.

Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China.

出版信息

Innovation (Camb). 2025 Jan 6;6(1):100754. doi: 10.1016/j.xinn.2024.100754.

Abstract

Heterogeneous catalysis at the metal surface generally involves the transport of molecules through the interfacial water layer to access the surface, which is a rate-determining step at the nanoscale. In this study, taking the oxygen reduction reaction on a metal electrode in aqueous solution as an example, using accurate molecular dynamic simulations, we propose a novel long-range regulation strategy in which midinfrared stimulation (MIRS) with a frequency of approximately 1,000 cm is applied to nonthermally induce the structural transition of interfacial water from an ordered to disordered state, facilitating the access of oxygen molecules to metal surfaces at room temperature and increasing the oxygen reduction activity 50-fold. Impressively, the theoretical prediction is confirmed by the experimental observation of a significant discharge voltage increase in zinc-air batteries under MIRS. This MIRS approach can be seamlessly integrated into existing strategies, offering a new approach for accelerating heterogeneous reactions and gas sensing within the interfacial water system.

摘要

金属表面的多相催化通常涉及分子通过界面水层传输以接近表面,这是纳米尺度上的速率决定步骤。在本研究中,以水溶液中金属电极上的氧还原反应为例,通过精确的分子动力学模拟,我们提出了一种新颖的远程调控策略,即施加频率约为1000 cm的中红外刺激(MIRS)以非热方式诱导界面水的结构从有序态转变为无序态,从而在室温下促进氧分子接近金属表面,并将氧还原活性提高50倍。令人印象深刻的是,通过实验观察到在MIRS下锌空气电池的放电电压显著增加,证实了理论预测。这种MIRS方法可以无缝集成到现有策略中,为加速界面水系统内的多相反应和气体传感提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a164/11764022/df25f6754fe7/fx1.jpg

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