2D carbide nanomeshes and their assembling into 3D microflowers for efficient water splitting

被引:116
作者
Kou, Zongkui [1 ]
Zhang, Lei [1 ]
Ma, Yuanyuan [1 ]
Liu, Ximeng [1 ]
Zang, Wenjie [1 ]
Zhang, Jian [2 ]
Huang, Shaozhuan [3 ]
Du, Yonghua [4 ]
Cheetham, Anthony K. [1 ]
Wang, John [1 ]
机构
[1] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117574, Singapore
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[3] Singapore Univ Technol & Design, Pillar Engn Prod Dev, Singapore 487372, Singapore
[4] ASTAR, Inst Chem & Engn Sci, 1 Pesek Rd, Singapore 627833, Singapore
关键词
Surface engineering; 2D carbide; Nanomesh; 3D assembly; Water splitting; HYDROGEN EVOLUTION REACTION; MOLYBDENUM CARBIDE; ENERGY-CONVERSION; ELECTROCATALYSTS; CATALYSTS; NANOSHEETS; DISULFIDE; NITRIDE; SURFACE; COBALT;
D O I
10.1016/j.apcatb.2018.11.008
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
Herein, we have developed a facile process of synthesizing N and O surface-terminated 2D molybdenum carbide nanomeshes (Mo2CTx NMs) and assembling them into 3D microflowers (Mo2CTx MFs) by one-step pyrolysis of Mo/Zn bimetallic imidazolate frameworks. When used as an oxygen evolution reaction (OER) catalyst, the Mo2CTx NMs thus derived exhibit outstanding catalytic activity with an overpotential of 180 mV at the current density of 10 mA cm(-2). This enables Mo2CTx NMs to become one of the best OER electrocatalysts ever reported, with the desired stability in alkaline environment which is a major challenge for most of the non-oxide/hydroxide based electrocatalyts. Additionally, the Mo2CTx MFs can catalyze the hydrogen evolution reaction (HER) and act as bifunctional electrocatalysts for overall water splitting which can attain a current density of 10 mA cm(-2) at 1.7 V. Mo LIII-edge X-ray near-edge absorption studies combined with theoretical calculations imply that surface-terminated oxygen is crucial in activating the outstanding OER performance, whereas the top Mo atomic sites on the surface contribute to excellent HER performance.
引用
收藏
页码:678 / 685
页数:8
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