Stabilized monolayer 1T MoS2 embedded in CoOOH for highly efficient overall water splitting

被引:39
作者
Shang, Bo [1 ,2 ]
Ma, Pengfei [1 ,2 ]
Fan, Jinchang [1 ,2 ]
Jiao, Lin [1 ,2 ]
Liu, Zijian [1 ,2 ]
Zhang, Zheyu [1 ,2 ]
Chen, Nuo [1 ,2 ]
Cheng, Zhiliang [3 ]
Cui, Xiaoqiang [1 ,2 ]
Zheng, Weitao [1 ,2 ]
机构
[1] Jilin Univ, Dept Mat Sci, State Key Lab Automot Simulat & Control, 2699 Qianjin St, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Key Lab Automobile Mat, MOE, 2699 Qianjin St, Changchun 130012, Jilin, Peoples R China
[3] Univ Penn, Dept Bioengn, 210 South 33rd St,240 Skirkanich Hall, Philadelphia, PA 19104 USA
关键词
HYDROGEN EVOLUTION; MOLYBDENUM-DISULFIDE; ULTRATHIN NANOSHEETS; PHASE-TRANSITION; EDGE SITES; ONE-POT; CATALYSTS; ELECTROCATALYSTS; HETEROSTRUCTURES; NANOPARTICLES;
D O I
10.1039/c8nr04218g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The complicated synthesis procedure and the unstable nature of 1T MoS2 vastly impede its practical application although it has shown a high performance for many different applications. Herein, we have synthesized ultrastable 1T phase MoS2 embedded in CoOOH by a facile one-pot strategy and achieved a high overall water splitting activity. The amorphous CoOOH in this heterostructure not only exhibits high oxygen evolution reaction activity, but also anchors and stabilizes the 1T MoS2 as vertically aligned single layers. This novel method gives new insight into developing stable and active atomically thin transition metal dichalcogenide heterostructures.
引用
收藏
页码:12330 / 12336
页数:7
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