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
膜
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
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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