TY - JOUR
T1 - Role of intrinsic dipole on photocatalytic water splitting for Janus MoSSe/nitrides heterostructure
T2 - A first-principles study
AU - Yin, Wenjin
AU - Wen, Bo
AU - Ge, Qingxia
AU - Zou, Daifeng
AU - Xu, Ying
AU - Liu, Mingwei
AU - Wei, Xiaolin
AU - Chen, Mingyang
AU - Fan, Xiaoli
N1 - Publisher Copyright:
© 2019 Chinese Materials Research Society
PY - 2019/6
Y1 - 2019/6
N2 - Searching for visible-infrared solar utilization for photocatalytic water splitting is highly desirable, since most of solar energy is distributed the visible-infrared region. However, it is difficult for a pure system to satisfy both band gap and band edge conditions for water splitting in visible-infrared region. Herein, heterostructure consisting of Janus MoSSe and nitrides XN (X = Al, Ga) is proposed, and the structural and electronic properties are systematically studied by the first-principles calculations. It shows that the AA-stacking heterostructure is more stable than other stacking. The calculated electronic property shows that MoSSe/AlN heterostructures have indirect band gaps in the range of 1.00 eV–1.68 eV, while MoSSe/GaN heterostructures are always direct semiconductors with band gaps of 0.8 eV–1.51 eV. Interestingly, despite the band gaps of MoSSe/XN heterostructures being smaller than 1.23 eV, the band edge positions are always suitable for water splitting, suggesting good activity of these heterostructures in visible-infrared region. This special behavior mainly originates from the intrinsic dipole with the electrons of VBM and CBM distributed on two opposite layers, producing an electrostatic potential difference between the layers. This electrostatic potential difference, acting as an auxiliary booster for photoinduced carriers, can effectively reduce the band gap required for water splitting in visible-infrared region. In addition, the band edge position can be further adjusted by strains, leading to higher reactivity for water splitting. Our findings strongly suggest that this novel Janus MoSSe/XN heterostructure can offer exciting opportunities for designing visible-infrared photocatalysis for water splitting.
AB - Searching for visible-infrared solar utilization for photocatalytic water splitting is highly desirable, since most of solar energy is distributed the visible-infrared region. However, it is difficult for a pure system to satisfy both band gap and band edge conditions for water splitting in visible-infrared region. Herein, heterostructure consisting of Janus MoSSe and nitrides XN (X = Al, Ga) is proposed, and the structural and electronic properties are systematically studied by the first-principles calculations. It shows that the AA-stacking heterostructure is more stable than other stacking. The calculated electronic property shows that MoSSe/AlN heterostructures have indirect band gaps in the range of 1.00 eV–1.68 eV, while MoSSe/GaN heterostructures are always direct semiconductors with band gaps of 0.8 eV–1.51 eV. Interestingly, despite the band gaps of MoSSe/XN heterostructures being smaller than 1.23 eV, the band edge positions are always suitable for water splitting, suggesting good activity of these heterostructures in visible-infrared region. This special behavior mainly originates from the intrinsic dipole with the electrons of VBM and CBM distributed on two opposite layers, producing an electrostatic potential difference between the layers. This electrostatic potential difference, acting as an auxiliary booster for photoinduced carriers, can effectively reduce the band gap required for water splitting in visible-infrared region. In addition, the band edge position can be further adjusted by strains, leading to higher reactivity for water splitting. Our findings strongly suggest that this novel Janus MoSSe/XN heterostructure can offer exciting opportunities for designing visible-infrared photocatalysis for water splitting.
UR - http://www.scopus.com/inward/record.url?scp=85069651309&partnerID=8YFLogxK
U2 - 10.1016/j.pnsc.2019.05.003
DO - 10.1016/j.pnsc.2019.05.003
M3 - 文章
AN - SCOPUS:85069651309
SN - 1002-0071
VL - 29
SP - 335
EP - 340
JO - Progress in Natural Science: Materials International
JF - Progress in Natural Science: Materials International
IS - 3
ER -