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掺杂锡提高了BiOCl纳米片在电催化合成过氧化氢方面的性能。

Doped-Sn Enhanced the Performance of BiOCl Nanosheet on Electrocatalytic Synthesis of Hydrogen Peroxide.

作者信息

Zhang Shijie, Wang Yabing, Jiang Chenghang, Li Yuanan, Bao Zhikang, Zhong Haochong, Fang Wenjuan, Wang Jianguo

机构信息

Institute of Industrial Catalysis, State Key Laboratory Breeding Base of Green-Chemical Synthesis Technology, Zhejiang University of Technology, Hangzhou, 310032, China.

出版信息

Small. 2024 Dec;20(49):e2403862. doi: 10.1002/smll.202403862. Epub 2024 Sep 23.

Abstract

The hydrogen peroxide (HO) produced through electrochemical two-electron oxygen reduction reaction (2e ORR) is a promising green synthesis method and served as potential strategy to replace the energy-intensive anthraquinone process. Nevertheless, the design of low-cost and efficient electrocatalysts for 2e ORR remains a formidable challenge. In this study, Sn-BiOCl nanosheets electrocatalysts are prepared for expediting the 2e ORR, achieving a high HO selectivity of 92.9%, and the HO yield of 10628 mg L h (0.1 mg cm) in a flow-cell device. The in situ ATR-SEIRAS results reveal that Sn-BiOCl enhances the adsorption and activation of *OOH compared to BiOCl, resulting in higher activity and selectivity for 2e ORR. Furthermore, this study investigates the potential for on-site production and application of HO using Sn-BiOCl, which displays a 95% degradation removal of dyes (RhB, MB, and MO) within 20 min. This work not only have an insight into the critical roles of Bi and Sn atoms in enhancing the catalytic performance but also provides a thought to design efficient catalysts for production HO via electrochemical 2e ORR.

摘要

通过电化学双电子氧还原反应(2e ORR)产生过氧化氢(HO)是一种很有前景的绿色合成方法,也是替代能源密集型蒽醌法的潜在策略。然而,设计用于2e ORR的低成本高效电催化剂仍然是一个巨大的挑战。在本研究中,制备了Sn-BiOCl纳米片电催化剂以加速2e ORR,在流动池装置中实现了92.9%的高HO选择性和10628 mg L h(0.1 mg cm)的HO产率。原位ATR-SEIRAS结果表明,与BiOCl相比,Sn-BiOCl增强了*OOH的吸附和活化,从而对2e ORR具有更高的活性和选择性。此外,本研究还研究了使用Sn-BiOCl现场生产和应用HO的潜力,其在20分钟内对染料(RhB、MB和MO)的降解去除率达95%。这项工作不仅深入了解了Bi和Sn原子在提高催化性能中的关键作用,还为通过电化学2e ORR生产HO设计高效催化剂提供了思路。

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