Cu-N4 single atoms derived from metal-organic frameworks with trapped nitrogen-rich molecules and their use as efficient electrocatalysts for oxygen reduction reaction

被引:56
作者
Lu, Fenghong [1 ]
Fan, Kaicai [2 ]
Cui, Lixiu [1 ]
Yang, Ye [1 ]
Wang, Wenxuan [1 ]
Zhang, Guitao [1 ]
Wang, Chengbin [1 ]
Zhang, Qi [1 ]
Li, Bin [3 ]
Zong, Lingbo [1 ]
Wang, Lei [1 ,4 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Eco Chem Engn, Taishan Scholar Adv & Characterist Discipline Tea, Qingdao 266042, Peoples R China
[2] Griffith Univ, Sch Environm & Sci, Ctr Clean Environm & Energy, Griffith, Qld, Australia
[3] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266042, Peoples R China
[4] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Shandong Engn Res Ctr Marine Environm Corros & Sa, Qingdao 266042, Peoples R China
关键词
Metal-Organic Frameworks; Single atom electrocatalysts; Oxygen reduction reaction; Nitrogen-rich molecules; Zn-air battery; NANOSHEETS; SITES;
D O I
10.1016/j.cej.2021.133242
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The development of noble-metal-free single atom electrocatalysts (SAECs) with both remarkable activity and durability for oxygen reduction reaction (ORR) are in great demand for large-scale commercialization of proton-exchange membrane fuel cells and metal-air batteries. Here, we developed a novel strategy to fabricate high-performance Cu-SAs/NSs from pyrolysis of two-dimensional (2D) Cu/Zn bimetallic MOF. Specifically, nitrogen-rich molecules (melamine) were deliberately added to intrigue the self-assembly of Cu/Zn bimetallic MOF, and contribute to the formation of highly porous structure and abundant Cu-N-4 active sites. With the enhanced accessibility of active sites and mass transport, the as-developed Cu-SAs/NSs display a remarkable ORR performance in alkaline media, outperforming the benchmark Pt/C and most of platinum group metals (PGMs)-free electrocatalysts reported to date. Notably, this facile strategy can be extended to fabricate other transition metal (TM, TM = Fe, Co, Ni)-based single atoms. This work presents a novel and general strategy to construct carbon-based SAECs towards ORR.
引用
收藏
页数:9
相关论文
共 58 条
[1]   "Wiring" Fe-Nx-Embedded Porous Carbon Framework onto 1D Nanotubes for Efficient Oxygen Reduction Reaction in Alkaline and Acidic Media [J].
Ahn, Sung Hoon ;
Yu, Xingwen ;
Manthiram, Arumugam .
ADVANCED MATERIALS, 2017, 29 (26)
[2]  
Ahsan M.A., J AM CHEM SOC, V143
[3]  
Chen Q., CHEM ENG J, V427
[4]   NiMn-Based Bimetal-Organic Framework Nanosheets Supported on Multi-Channel Carbon Fibers for Efficient Oxygen Electrocatalysis [J].
Cheng, Weiren ;
Lu, Xue Feng ;
Luan, Deyan ;
Lou, Xiong Wen .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (41) :18234-18239
[5]   Rational design of ultrahigh loading metal single-atoms (Co, Ni, Mo) anchored on in-situ pre-crosslinked guar gum derived N-doped carbon aerogel for efficient overall water splitting [J].
Cheng, Yu ;
Guo, Haoran ;
Li, Xinpan ;
Wu, Xiao ;
Xu, Xiaohui ;
Zheng, Lirong ;
Song, Rui .
CHEMICAL ENGINEERING JOURNAL, 2021, 410 (410)
[6]   Direct atomic-level insight into the active sites of a high-performance PGM-free ORR catalyst [J].
Chung, Hoon T. ;
Cullen, David A. ;
Higgins, Drew ;
Sneed, Brian T. ;
Holby, Edward F. ;
More, Karren L. ;
Zelenay, Piotr .
SCIENCE, 2017, 357 (6350) :479-483
[7]   Electrocatalyst approaches and challenges for automotive fuel cells [J].
Debe, Mark K. .
NATURE, 2012, 486 (7401) :43-51
[8]  
Du Y., 2019, ANGEW CHEM INT EDIT, V58
[9]   Single atom electrocatalysts supported on graphene or graphene-like carbons [J].
Fei, Huilong ;
Dong, Juncai ;
Chen, Dongliang ;
Hu, Tiandou ;
Duan, Xidong ;
Shakir, Imran ;
Huang, Yu ;
Duan, Xiangfeng .
CHEMICAL SOCIETY REVIEWS, 2019, 48 (20) :5207-5241
[10]   A Mn-N3 single-atom catalyst embedded in graphitic carbon nitride for efficient CO2 electroreduction [J].
Feng, Jiaqi ;
Gao, Hongshuai ;
Zheng, Lirong ;
Chen, Zhipeng ;
Zeng, Shaojuan ;
Jiang, Chongyang ;
Dong, Haifeng ;
Liu, Licheng ;
Zhang, Suojiang ;
Zhang, Xiangping .
NATURE COMMUNICATIONS, 2020, 11 (01)