Atomically precise Ni6(SC2H4Ph)12 nanoclusters on graphitic carbon nitride nanosheets for boosting photocatalytic hydrogen evolution

被引:16
|
作者
Wei, Jieding [1 ]
Zhao, Renqiang [1 ]
Luo, Dian [1 ]
Lu, Xiangyu [1 ]
Dong, Wenxiu [1 ]
Huang, Yucheng [1 ]
Cheng, Xiaomei [2 ]
Ni, Yonghong [1 ]
机构
[1] Anhui Normal Univ, Coll Chem & Mat Sci, Key Lab Funct Mol Solids, Anhui Lab Mol Based Mat, 189 Jiuhua Southern Rd, Wuhu 241002, Peoples R China
[2] WanNan Med Coll, Dept Chem, Wuhu 241000, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphitic carbon nitride; Atomically precise nanoclusters; Ni-6(SC2H4Ph)(12) nanoclusters; Photocatalytic hydrogen evolution; WATER; EFFICIENT; G-C3N4; COCATALYST; COMPOSITES; SUPPORT; ROBUST;
D O I
10.1016/j.jcis.2022.11.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Much effort has been devoted to improving the photocatalytic capacity of graphitic carbon nitride (g-C3N4). In this paper, we reported the successful synthesis of a hybrid photocatalyst with superb pho-tocatalytic hydrogen production activity through decorating atomically precise Ni6(SC2H4Ph)12 nanoclus-ters on g-C3N4 nanosheets (labeled as Ni6/g-C3N4) at room temperature. Zeta potential experiments demonstrated that the electrostatic interaction between Ni6 and g-C3N4 led to the formation of Ni6/g-C3N4. The photocatalytic measurements revealed that the 5 %-Ni6/g-C3N4 prepared with the origi-nal mass ratio of m(Ni6)/m(g-C3N4) = 1/20 exhibited the strongest hydrogen production activity. In the system with triethanolamine (TEOA) as the sacrifice agent, the visible-light hydrogen production rate reached up to 5.87 mmol h-1 g-1, approximately 290 times higher than that of pure g-C3N4 (0.02 mmol h-1 g-1). Density functional theory (DFT) calculations testified that the above significant enhancement of photocatalytic hydrogen evolution of the hybrid photocatalyst arose from the photogen-erated electrons transfer from Ni6 to g-C3N4.(c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:212 / 221
页数:10
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