CoTe nanoparticle-embedded N-doped hollow carbon polyhedron: an efficient catalyst for HO electrosynthesis in acidic media

Rational design and development of high-efficiency electrocatalytic materials made from earth-abundant elements for H 2 O 2 generation via a two-electron O 2 reduction reaction (2e − ORR) is of crucial significance but still challenging. Here, we demonstrate that CoTe nanoparticles embedded in a nit...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-10, Vol.9 (38), p.2173-2177
Hauptverfasser: Zhang, Longcheng, Liang, Jie, Yue, Luchao, Dong, Kai, Xu, Zhaoquan, Li, Tingshuai, Liu, Qian, Luo, Yonglan, Liu, Yang, Gao, Shuyan, Asiri, Abdullah M, Kong, Qingquan, Guo, Xiaodong, Sun, Xuping
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Zusammenfassung:Rational design and development of high-efficiency electrocatalytic materials made from earth-abundant elements for H 2 O 2 generation via a two-electron O 2 reduction reaction (2e − ORR) is of crucial significance but still challenging. Here, we demonstrate that CoTe nanoparticles embedded in a nitrogen-doped hollow carbon polyhedron (CoTe@NC) can be adopted as a highly selective and stable 2e − ORR electrocatalyst. Benefiting from the synergistic effect between the highly active CoTe nanoparticles and nitrogen-doped hollow carbon polyhedron, in 0.1 M HClO 4 , the CoTe@NC hybrid exhibits superb electrocatalytic activity toward the 2e − ORR with high selectivity of up to 92.6% and a large H 2 O 2 production rate of 297.9 ppm h −1 at −0.044 V versus reversible hydrogen electrode. Moreover, it operates rather stably under the working conditions with a negligible current decrease after 12 h. Theoretical calculations further provide insight into the catalytic mechanism involved . CoTe nanoparticles embedded nitrogen-doped hollow carbon polyhedron (CoTe@NC) acts as a highly efficient 2e − O 2 reduction reaction electrocatalyst with a high selectivity of up to 92.6% at 0.3 V, significantly outperforming CoTe and NC counterparts.
ISSN:2050-7488
2050-7496
DOI:10.1039/d1ta06313h