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通过基于导电镍酞菁的共价有机框架连续电合成具有医用级浓度的纯过氧化氢溶液。

Continuous Electrosynthesis of Pure HO Solution with Medical-Grade Concentration by a Conductive Ni-Phthalocyanine-Based Covalent Organic Framework.

作者信息

Zhang Meng-Di, Huang Jia-Run, Liang Cheng-Peng, Chen Xiao-Ming, Liao Pei-Qin

机构信息

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, GBRCE for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou 510275, China.

Chemistry and Chemical Engineering Guangdong Laboratory, Shantou 515021, China.

出版信息

J Am Chem Soc. 2024 Nov 13;146(45):31034-31041. doi: 10.1021/jacs.4c10675. Epub 2024 Nov 4.

DOI:10.1021/jacs.4c10675
PMID:39495344
Abstract

Electrosynthesis of HO provides an environmentally friendly alternative to the traditional anthraquinone method employed in industry, but suffers from impurities and restricted yield rate and concentration of HO. Herein, we demonstrated a Ni-phthalocyanine-based covalent-organic framework (COF, denoted as ) with a higher inherent conductivity of 1.14 × 10 S m, which exhibited an ultrahigh current density of 530 mA cm with a Faradaic efficiency (HO) of ∼100% at a low cell voltage of 3.5 V. Notably, this high level of performance is maintained over a continuous operation of 200 h without noticeable degradation. When integrated into a scale-up membrane electrode assembly electrolyzer and operated at ∼3300 mA at a very low cell voltage of 2 V, continuously yielded a pure HO solution with medical-grade concentration (3.5 wt %), which is at least 3.5 times higher than previously reported catalysts and 1.5 times the output of the traditional anthraquinone process. A mechanistic study revealed that enhancing the π-conjugation to reduce the band gap of the molecular catalytic sites integrated into a COF is more effective to enhance its inherent electron transport ability, thereby significantly improving the electrocatalytic performance for HO generation.

摘要

通过电合成过氧化氢为工业上采用的传统蒽醌法提供了一种环境友好的替代方法,但存在杂质问题,且过氧化氢的产率和浓度受到限制。在此,我们展示了一种基于镍酞菁的共价有机框架(COF,记为 ),其固有电导率较高,为1.14×10 S m,在3.5 V的低电池电压下表现出530 mA cm的超高电流密度,法拉第效率(生成过氧化氢)约为100%。值得注意的是,在连续运行200 h的过程中,这种高水平的性能得以保持,且没有明显降解。当集成到放大的膜电极组件电解槽中,并在2 V的极低电池电压下以约3300 mA运行时, 持续产生医疗级浓度(3.5 wt%)的纯过氧化氢溶液,这至少比先前报道的催化剂高出3.5倍,是传统蒽醌法产量的1.5倍。机理研究表明,增强π共轭以降低集成到COF中的分子催化位点的带隙,对于提高其固有电子传输能力更有效,从而显著提高生成过氧化氢的电催化性能。

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