TY - JOUR
T1 - Interfacial coupled engineering of plasmonic amorphous MoO3-x nanodots/g-C3N4 nanosheets for photocatalytic water splitting and photothermal conversion
AU - Ren, Yumei
AU - Feng, Desheng
AU - Yan, Zhiming
AU - Sun, Zixu
AU - Zhang, Zixuan
AU - Xu, Dongwei
AU - Qiao, Chong
AU - Chen, Zhonghui
AU - Jia, Yu
AU - Chan Jun, Seong
AU - Liu, Shude
AU - Yamauchi, Yusuke
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/2/1
Y1 - 2023/2/1
N2 - Semiconductor-based plasmonic materials have attracted extensive attention for photocatalytic systems. However, their photocatalytic reactions are hindered by limited light-harvesting ability and the transfer rate of photo-generated electrons. Herein, vacancy engineering and phase engineering are rationally integrated to develop amorphous molybdenum oxide (a-MoO3−x) nanodots anchored on g-C3N4 as a highly active photocatalyst. Through high localized surface plasmon resonance (LSPR) effect of a-MoO3−x nanodots and tunable electrical properties induced by the heterostructural interface, the Z-scheme a-MoO3−x/g-C3N4 heterostructure demonstrates broadband absorption and the excited photo-generated electrons. Further theoretical calculations demonstrate that the enhancement of photocatalytic and photothermal performance is mainly attributed to the highly localized Anderson tail states of a-MoO3−x. Consequently, the a-MoO3−x/g-C3N4 heterostructure exhibits a photocurrent density of ∼36.5 μA cm−2, which is about 2.7 and 4.1 times higher than that of pure g-C3N4 nanosheets (∼13.5 μA cm−2) and a-MoO3−x nanodots (∼9 μA cm−2), respectively. The photocatalytic performance enhancement relying on defects and long-range disorder of a-MoO3−x in Z-scheme heterostructure is explored.
AB - Semiconductor-based plasmonic materials have attracted extensive attention for photocatalytic systems. However, their photocatalytic reactions are hindered by limited light-harvesting ability and the transfer rate of photo-generated electrons. Herein, vacancy engineering and phase engineering are rationally integrated to develop amorphous molybdenum oxide (a-MoO3−x) nanodots anchored on g-C3N4 as a highly active photocatalyst. Through high localized surface plasmon resonance (LSPR) effect of a-MoO3−x nanodots and tunable electrical properties induced by the heterostructural interface, the Z-scheme a-MoO3−x/g-C3N4 heterostructure demonstrates broadband absorption and the excited photo-generated electrons. Further theoretical calculations demonstrate that the enhancement of photocatalytic and photothermal performance is mainly attributed to the highly localized Anderson tail states of a-MoO3−x. Consequently, the a-MoO3−x/g-C3N4 heterostructure exhibits a photocurrent density of ∼36.5 μA cm−2, which is about 2.7 and 4.1 times higher than that of pure g-C3N4 nanosheets (∼13.5 μA cm−2) and a-MoO3−x nanodots (∼9 μA cm−2), respectively. The photocatalytic performance enhancement relying on defects and long-range disorder of a-MoO3−x in Z-scheme heterostructure is explored.
KW - Amorphous MoO nanodots
KW - Photocatalytic water splitting
KW - Photothermal conversion
KW - Surface plasmon effect
KW - g-CN nanosheets
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U2 - 10.1016/j.cej.2022.139875
DO - 10.1016/j.cej.2022.139875
M3 - Article
AN - SCOPUS:85140305456
SN - 1385-8947
VL - 453
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 139875
ER -