Magnetic Activation: A Novel Approach to Enhance Hydrogen Evolution Activity of Co 0.85 Se@CNTs Heterostructured Catalyst

The heterostructure strategy is currently an effective method for enhancing the catalytic activity of materials. However, the challenge that is how to further improve their catalytic performance, based on the principles of material modification is must addressed. Herein, a strategy is introduced for...

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Veröffentlicht in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-11, Vol.20 (48), p.e2405838
Hauptverfasser: Xue, Hongyao, Wang, Jiacheng, Li, Xiyue, Liu, Ziqi, Zhang, Haiqin, Zhang, Yaowen, Zhang, Yixue, Pan, Jiajing, Han, Mei, He, Yan
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Sprache:eng
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Zusammenfassung:The heterostructure strategy is currently an effective method for enhancing the catalytic activity of materials. However, the challenge that is how to further improve their catalytic performance, based on the principles of material modification is must addressed. Herein, a strategy is introduced for magnetically regulating the catalytic activity to further enhance the hydrogen evolution reaction (HER) activity for Co Se@CNTs heterostructured catalyst. Building on heterostructure modulation, an external alternating magnetic field (AMF) is introduced to enhance the electronic localization at the active sites, which significantly boosts catalytic performance (71 to 43 mV at 10 mA cm ). To elucidate the catalytic mechanism, especially under the influence of the AMF, in situ Raman spectroscopy is innovatively applied to monitor the HER process of Co Se@CNTs, comparing conditions with and without the AMF. This study demonstrates that introducing the AMF does not induce a change in the true active site. Importantly, it shows that the Lorentz force generated by the AMF enhances HER activity by promoting water molecule adsorption and O─H bond cleavage, with the Stark tuning rate indicating increased water interaction and bond cleavage efficiency. Theoretical calculations further support that the AMF optimizes energy barriers for key reaction intermediates (steps of H O-TS and H+ 1/2H ).
ISSN:1613-6810
1613-6829
DOI:10.1002/smll.202405838