Porous heterostructure of h-BN/carbon as an efficient electrocatalyst for hydrogen peroxide generation

被引:2
作者
Xu, Xiang [1 ]
Zhao, Yuying [2 ]
Yuan, Qixin [1 ]
Wu, Yuhan [1 ]
He, Jiawei [1 ]
Fan, Mengmeng [1 ,2 ]
机构
[1] Nanjing Forestry Univ, Coll Chem Engn, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Int Innovat Ctr Forest Chem & Mat, 159 Longpan Rd, Nanjing 210037, Peoples R China
[2] Chinese Acad Forestry, Inst Chem Ind Forest Prod, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Key Lab Biomass Energy & Mat, 16 Suojin Wucun Rd, Nanjing 210042, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Heterostructure; Hydrogen peroxide synthesis; h-BN/carbon; Oxygen reduction reaction; 2e(-) pathway; HEXAGONAL BORON-NITRIDE; OXYGEN REDUCTION; H2O2; CATALYSTS;
D O I
10.1007/s42823-024-00718-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We successfully synthesized a porous carbon material with abundant hexagonal boron nitride (h-BN) dispersed on a carbon matrix (p-BN-C) as efficient electrocatalysts for two-electron oxygen reduction reaction (2e(-) ORR) to produce hydrogen peroxide (H2O2). This catalyst was fabricated via ball-milling-assisted h-BN exfoliation and subsequent growth of carbon structure. In alkaline solutions, the h-BN/carbon heterostructure exhibited superior electrocatalytic activity for H2O2 generation measured by a rotating ring-disk electrode (RRDE), with a remarkable selectivity of up to 90-97% in the potential range of 0.3-0.6 V vs reversible hydrogen electrode (RHE), superior to most of the reported carbon-based electrocatalysts. Density functional theory (DFT) simulations indicated that the B atoms at the h-BN heterostructure interface were crucial active sites. These results underscore the remarkable catalytic activity of heterostructure and provide a novel approach for tailoring carbon-based catalysts, enhancing the selectivity and activity in the production of H2O2 through heterostructure engineering.
引用
收藏
页码:1629 / 1637
页数:9
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