Synergetic Effects toward Catalysis and Confinement of Magnesium Hydride on Modified Graphene: A First-Principles Study

Citation data:

The Journal of Physical Chemistry C, ISSN: 1932-7447, Vol: 121, Issue: 34, Page: 18401-18411

Publication Year:
2017
Captures 3
Readers 3
Repository URL:
http://ro.uow.edu.au/aiimpapers/2727
DOI:
10.1021/acs.jpcc.7b05848
Author(s):
Zhang, Jian; Xia, Guanglin; Guo, Zaiping; Zhou, Dianwu
Publisher(s):
American Chemical Society (ACS)
Tags:
Materials Science; Energy; Chemistry; Engineering; Physical Sciences and Mathematics
article description
Graphene nanosheet has recently demonstrated catalytic and agglomeration blocking effects toward MgH nanoparticles. Nevertheless, there is a very limited understanding of the relationship between the structural characteristics of graphene nanosheet and the hydrogen sorption properties of MgH nanoparticles. Using first-principles calculations, we investigate the structural, energetic, and electronic properties of MgH clusters supported on pristine and modified graphene with carbon vacancy or heteroatom (B, N, Si, P, S, Fe, Co, Ni, and Al) doping. The results show that the formation ability of vacancy and heteroatom defects in the graphene lattice is enhanced in the order of vacancy, Al, Ni, S, Co, Fe, Si, P, B, and N. Among them, the B- and P-doped graphene nanosheets, especially the B-doped one, exhibit remarkable synergetic effects toward enhancing the catalysis and confinement of MgH hydride. Analysis of electronic structures shows that the direct bonding between MgH clusters and B/P-doped graphene and the electron transfer from MgH clusters into the B/P-doped graphene are most likely to be the underlying reasons for the improved dispersion and enhanced dehydrogenation properties of MgH clusters.