硼
氧气
还原(数学)
碳纤维
材料科学
化学
有机化学
几何学
数学
复合数
复合材料
作者
Xia Yang,Xunhua Zhao,Chuan Xia,Zhenyu Wu,Peng Zhu,Jung Yoon Kim,Xiaowan Bai,Guanhui Gao,Yongfeng Hu,Jun Zhong,Yuanyue Liu,Haotian Wang
标识
DOI:10.1038/s41467-021-24329-9
摘要
Abstract Oxygen reduction reaction towards hydrogen peroxide (H 2 O 2 ) provides a green alternative route for H 2 O 2 production, but it lacks efficient catalysts to achieve high selectivity and activity simultaneously under industrial-relevant production rates. Here we report a boron-doped carbon (B-C) catalyst which can overcome this activity-selectivity dilemma. Compared to the state-of-the-art oxidized carbon catalyst, B-C catalyst presents enhanced activity (saving more than 210 mV overpotential) under industrial-relevant currents (up to 300 mA cm −2 ) while maintaining high H 2 O 2 selectivity (85–90%). Density-functional theory calculations reveal that the boron dopant site is responsible for high H 2 O 2 activity and selectivity due to low thermodynamic and kinetic barriers. Employed in our porous solid electrolyte reactor, the B-C catalyst demonstrates a direct and continuous generation of pure H 2 O 2 solutions with high selectivity (up to 95%) and high H 2 O 2 partial currents (up to ~400 mA cm −2 ), illustrating the catalyst’s great potential for practical applications in the future.
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