4.8 Article

Flow-Through Electrochemical Membrane Reactor with a Self-Supported Carbon Membrane Electrode for Highly Efficient Synthesis of Hydrogen Peroxide

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 15, 期 36, 页码 42460-42469

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.3c06307

关键词

carbon membrane; in situ electrosynthesis H2O2; oxygen reduction reaction; disorderedcarbon; flow-through electrochemical membrane reactor

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This study successfully synthesized H2O2 efficiently and cost-effectively by using a self-supported carbon membrane as the cathode in a flow-through electrochemical membrane reactor.
In situ electroreduction of O-2 to H2O2 by using electrons as reagents is known as a green process, which is highly desirable for environmental remediation and chemical industries. However, the development of a cost-effective electrode with superior H2O2 synthesis rate and stability is challenging. A self-supported carbon membrane (CM) was prepared in this study from activated carbon and phenolic resin by carbonization under a H-2 atmosphere. It was employed as the cathode to build a flow-through electrochemical membrane reactor (FT-ECMR) for electrosynthesis of H2O2. The results showed that the CM had a small pore size (34 nm), a high porosity (42.3%), and a high surface area (450.7 m(2) g(-1)). In contrast to most of the state-of-the-art self-supported carbon electrode reported in the previous works, the FT-ECMR exhibited a high concentration of continuous and stable H2O2 electrosynthesis (1042 mg L-1) as well as a H2O2 synthesis rate of 5.21 mg h(-1) cm(-2). It had also demonstrated a high oxygen conversion (0.37%) and current efficiency (88%). The outstanding performance of the FT-ECMR for H2O2 synthesis was attributed to the enhanced mass transfer of the reactor, the existence of a relatively high surface area of CM, and the abundant disordered carbon structures (sp(3)-C, defects, and edges). In conclusion, our work highlighted using the FT-ECMR with the CM to synthesize H2O2 efficiently and cost-effectively.

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