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γ-二氧化锰作为RuO在酸性介质中析氧催化剂的电子储存库。

γ-MnO as an Electron Reservoir for RuO Oxygen Evolution Catalyst in Acidic Media.

作者信息

Jia Wenqi, Cao Xuejie, Chen Xiaojie, Qin Hongye, Miao Licheng, Wang Qinglun, Jiao Lifang

机构信息

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), College of Chemistry, Nankai University, Tianjin, 300071, China.

出版信息

Small. 2024 Aug;20(34):e2310464. doi: 10.1002/smll.202310464. Epub 2024 Apr 10.

Abstract

Developing highly active and durable catalysts in acid conditions remains an urgent issue due to the sluggish kinetics of oxygen evolution reaction (OER). Although RuO has been a state-of-the-art commercial catalyst for OER, it encounters poor stability and high cost. In this study, the electronic reservoir regulation strategy is proposed to promote the performance of acidic water oxidation via constructing a RuO/MnO heterostructure supported on carbon cloth (CC) (abbreviated as RuO/MnO/CC). Theoretical and experimental results reveal that MnO acts as an electron reservoir for RuO. It facilitates electron transfer from RuO, enhancing its activity prior to OER, and donates electrons to RuO, improving its stability after OER. Consequently, RuO/MnO/CC exhibits better performance compared to commercial RuO, with an ultrasmall overpotential of 189 mV at 10 mA cm and no signs of deactivation even after 800 h of electrolysis in 0.5 m HSO at 10 mA cm. When applied as the anode in a proton exchange membrane water electrolyzer, the cost-efficient RuO/MnO/CC catalyst only requires a cell voltage of 1.661 V to achieve the water-splitting current of 1 A cm, and the noble metal cost is as low as US$ 0.00962 cm, indicating potential for practical applications.

摘要

由于析氧反应(OER)动力学缓慢,开发在酸性条件下具有高活性和耐久性的催化剂仍然是一个紧迫的问题。尽管RuO一直是用于OER的最先进的商业催化剂,但它存在稳定性差和成本高的问题。在本研究中,提出了电子储存库调控策略,通过构建负载在碳布(CC)上的RuO/MnO异质结构(简称为RuO/MnO/CC)来提高酸性水氧化的性能。理论和实验结果表明,MnO作为RuO的电子储存库。它促进电子从RuO转移,增强其在OER之前的活性,并向RuO提供电子,提高其在OER之后的稳定性。因此,RuO/MnO/CC与商业RuO相比表现出更好的性能,在10 mA cm时具有189 mV的超小过电位,即使在0.5 m HSO中以10 mA cm进行800 h电解后也没有失活迹象。当用作质子交换膜水电解槽的阳极时,具有成本效益的RuO/MnO/CC催化剂仅需要1.661 V的电池电压即可实现1 A cm的水分解电流,贵金属成本低至0.00962美元/cm,表明具有实际应用潜力。

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