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

电合成 材料科学 碳化 电化学 膜反应器 化学工程 阴极 碳纤维 电极 过氧化氢 试剂 有机化学 复合材料 化学 扫描电子显微镜 生物化学 物理化学 复合数 工程类
作者
Zishang Chen,Hong Wang,Xiaohua Ma,Xiaoping Chen,Su Gui,Jianxin Li
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (36): 42460-42469
标识
DOI:10.1021/acsami.3c06307
摘要

In situ electroreduction of O2 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 H2 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 m2 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 (sp3-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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