Enhanced electroproduction of hydrogen peroxide with oxidized boron-doped carbon catalysts synthesized from gaseous CO 2

被引:6
|
作者
Yun, Won Chan [1 ]
Yang, Jeongwoo [1 ]
Lee, Dayeon [1 ]
Lee, Jimin [1 ]
Kim, Jongmin [2 ]
Byeon, Ayeong [3 ]
Lee, Jae W. [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Chem & Biomol Engn, 291 Daehak Ro, Daejeon 34141, South Korea
[2] Kyung Hee Univ, KHU KIST Dept Converging Sci & Technol, Seoul 02447, South Korea
[3] Chungbuk Natl Univ, Dept Chem Engn, Cheongju 28644, Chungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Oxidized boron sites; CO 2-derived carbon; Hydrogen peroxide; Oxygen reduction reaction; Electrocatalyst; OXYGEN REDUCTION; POROUS CARBON; NITROGEN; EFFICIENCY; ELECTRODE; DIOXIDE; SULFUR;
D O I
10.1016/j.jcou.2024.102833
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As an eco-friendly alternative to the conventional anthraquinone process, electrochemical production of hydrogen peroxide (H2O2) through the oxygen reduction reaction has been attracting attention. The goal of this work is to derive a carbon-based material from carbon dioxide (CO2) to achieve high performance in electrochemical H2O2 production. Doping heterogeneous element such as oxygen on a carbon catalyst has been mainly explored to increase the selectivity and activity, but little research has been conducted on enhancing catalytic activity with oxidized boron insertion. This study proposes porous carbon materials synthesized from CO2 as electrocatalysts. Polyethylene oxide (PEO) was thermally treated together to increase the boron-oxygen bonding sites. As a result, the synthesized carbon materials having oxidized boron functional groups of BC2O and BCO2 showed high activity (1.25 mA cm(-)(2)) and selectivity (similar to 90 %) over a wide voltage range in two-electron ORR (Oxygen Reduction Reaction) at alkaline media. Furthermore, in an H-cell where 0.4 V vs. RHE was applied, the average H2O2 production rate was maintained at 452.96 mmol g(-1) h(-1) for four hours with a high faraday efficiency of 90 %.
引用
收藏
页数:11
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