Carbon flowers as electrocatalysts for the reduction of oxygen to hydrogen peroxide

被引:11
作者
Gong, Huaxin [1 ,2 ]
Wei, Lingze [1 ,2 ]
Chen, Shucheng [1 ,2 ]
Chen, Zhihua [1 ,2 ]
Jaramillo, Thomas F. [1 ,2 ]
Bao, Zhenan [1 ,2 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, Menlo Pk, CA 94025 USA
基金
美国国家科学基金会;
关键词
carbon materials; H2O2; oxygen reduction reaction; nanostructures; NITROGEN-DOPED CARBON; CATALYSTS; SELECTIVITY; GENERATION; GRAPHENE;
D O I
10.1007/s12274-023-5903-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Small-scale and decentralized production of H2O2 via electrochemical reduction of oxygen is of great benefit, especially for sanitization, air and water purification, as well as for a variety of chemical processes. The development of low-cost and high-performance catalysts for this reaction remains a key challenge. Carbon-based materials have drawn substantial research efforts in recent years due to their advantageous properties, such as high chemical stability and high tunability in active sites and morphology. Deeper understanding of structure-activity relationships can guide the design of improved catalysts. We hypothesize that mass transport to active sites is of great importance, and herein we use carbon materials with unique flower-like superstructures to achieve high activity and selectivity for O-2 reduction to H2O2. The abundance of nitrogen active sites controlled by pyrolysis temperature resulted in high catalytic activity and selectivity for oxygen reduction reaction (ORR). The flower superstructure showed higher performance than the spherical nanoparticles due to greater accessibility to the active sites. Chemical activation improves the catalysts' performances further, driving the production of H2O2 to a record-setting rate of 816 mmol center dot gcat-1 center dot h-1 using a bulk electrolysis setup. This work demonstrates the development of a highly active catalyst for the sustainable production of H2O2 through rational design and synthetic control. The understanding from this work provides further insight into the design of future carbon-based electrocatalysts.
引用
收藏
页码:11556 / 11563
页数:8
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