Rational Design of Holey 2D Nonlayered Transition Metal Carbide/Nitride Heterostructure Nanosheets for Highly Efficient Water Oxidation

被引:223
|
作者
Kou, Zongkui [1 ]
Wang, Tingting [2 ]
Gu, Qilin [1 ]
Xiong, Mo [3 ]
Zheng, Lirong [4 ]
Li, Xin [1 ]
Pan, Zhenghui [1 ]
Chen, Hao [1 ]
Verpoort, Francis [2 ,5 ]
Cheetham, Anthony K. [1 ]
Mu, Shichun [2 ]
Wang, John [1 ]
机构
[1] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117574, Singapore
[2] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[3] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Hubei, Peoples R China
[4] Chinese Acad Sci, Beijing Synchrotron Radiat Facil, Inst High Energy Phys, Beijing 100049, Peoples R China
[5] Natl Res Tomsk Polytech Univ, Lenin Ave 30, Tomsk 634050, Russia
关键词
2D nonlayered structure; carbide; heterostructure; nitride; water splitting; HYDROGEN; ELECTROCATALYSTS; NANOPARTICLES; EXFOLIATION; CATALYSTS;
D O I
10.1002/aenm.201803768
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
Due to integrated advantages in electrochemical functionalities for energy conversion, 2D nonlayered heterostructure nanosheets offer new and fascinating opportunities for electrocatalysis but their fabrication is challenging when compared with the widely studied 2D layered heterostructure. Herein, a bottom-up approach is established for facile synthesis of holey 2D transition metal carbide/nitride heterostructure nanosheets (h-TMCN) with regulated hole sizes by controlled thermal annealing of the Mo/Zn bimetallic imidazolate frameworks (Mo/Zn BIFs). Ex situ phase and structural identifications disclose that the Mo/Zn BIFs precursor experiences interconnected three steps of transformation to produce h-TMCN. Especially, the slow successive solid-state diffusion of nitrogen and carbon into immediate noncrystalline molybdenum oxides allows the intergrowth of Mo2C and Mo2N into the 2D nonlayered heterostructure. X-ray fine structure analysis coupled with high resolution X-ray photoelectron spectroscopy demonstrate that Mo2C and Mo2N in the microdomains can chemically bond with each other, producing the abundant active N-Mo-C interfaces toward water splitting. Consequently, h-TMCN affords low overpotentials, high turnover frequencies, rapid charge transfer, and superior long-term stability toward electrocatalytic water oxidation. The present work demonstrates the feasibility of developing a broad range of 2D nonlayered heterostructures for high efficiency chemical energy conversion.
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页数:10
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