Oxygen‐Molecule Adsorption and Dissociation on BCN Graphene: A First‐Principles Study

• Published in: Chemphyschem 2017-01, Vol.18 (1), p.101-110
• Main Authors: Tang, Shaobin, Wu, Weihua, Liu, Liangxian, Gu, Junjing
• Format: Article
• Language: English
• Subjects: active catalytic sites; Adsorption; boron–nitrogen cluster doping; density functional calculations; graphene; Oxygen; oxygen molecule dissociation; Principles
• ISSN: 1439-4235; 1439-7641
• DOI: 10.1002/cphc.201600777

Boron and nitrogen co‐doped (BCN) graphene is an attractive material for use as a metal‐free oxygen reduction reaction electrocatalyst and as other catalysts due to its unique structure and electronic properties. Reported here is the structure, determined by using density functional theory, of the active O2‐dissociation site of BCN graphene containing different types of BN cluster. The results show that the edge termination and shape of substitutional BN clusters are two important factors that determine the catalytic activity of BCN graphene for the dissociation of molecular oxygen. N‐Terminated triangular BN (t‐BN) cluster doping can reduce the energy barrier more effectively compared to a t‐BN with a B edge or quadrangular BN cluster. Interestingly, the B atom neighboring the N edge, only in the case of N‐terminated t‐BN doping, is determined to be the most active site for O2 dissociation due to the barrier being as low as 0.08 eV. The electronic structure calculations reveal that in addition to the large positive charge densities, the catalytic activity of graphene enhanced by B,N doping is also attributed to the increased density of states of the π* states of the active site around the Fermi level. B more active: As determined by DFT calculations, both the edge termination and the shape of embedded BN clusters determine the activity of B,N co‐doped graphene for the catalysis of molecular oxygen dissociation. The boron atom neighboring the N edge of triangular‐BN‐cluster‐doped graphene is likely to be the most catalytically active site.