Design Principles for Covalent Organic Frameworks as Efficient Electrocatalysts in Clean Energy Conversion and Green Oxidizer Production

被引:217
作者
Lin, Chun-Yu [1 ]
Zhang, Lipeng [1 ]
Zhao, Zhenghang [1 ]
Xia, Zhenhai [1 ,2 ]
机构
[1] Univ North Texas, Dept Chem, Dept Mat Sci & Engn, Denton, TX 76203 USA
[2] Beijing Univ Chem Technol, Coll Energy, Beijing 100029, Peoples R China
基金
美国国家科学基金会;
关键词
OXYGEN EVOLUTION REACTIONS; AUGMENTED-WAVE METHOD; FUEL-CELL; SPLITTING DIAGRAMS; BASIS-SET; REDUCTION; CATALYSTS; METALS; OXIDE; COMPLEXES;
D O I
10.1002/adma.201606635
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Covalent organic frameworks (COFs), an emerging class of framework materials linked by covalent bonds, hold potential for various applications such as efficient electrocatalysts, photovoltaics, and sensors. To rationally design COF-based electrocatalysts for oxygen reduction and evolution reactions in fuel cells and metal-air batteries, activity descriptors, derived from orbital energy and bonding structures, are identified with the first-principle calculations for the COFs, which correlate COF structures with their catalytic activities. The calculations also predict that alkaline-earth metal-porphyrin COFs could catalyze the direct production of H2O2, a green oxidizer and an energy carrier. These predictions are supported by experimental data, and the design principles derived from the descriptors provide an approach for rational design of new electrocatalysts for both clean energy conversion and green oxidizer production.
引用
收藏
页数:7
相关论文
共 40 条
[1]   Self-assembled monolayers of cobalt(II)-(4-tert-butylphenyl)-porphyrins:: The influence of the electronic dipole on scanning tunneling microscopy images [J].
Arima, V ;
Fabiano, E ;
Blyth, RIR ;
Delia Sala, F ;
Matino, F ;
Thompson, J ;
Cingolani, R ;
Rinaldi, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (51) :16951-16958
[2]   Thiophene-based covalent organic frameworks [J].
Bertrand, Guillaume H. V. ;
Michaelis, Vladimir K. ;
Ong, Ta-Chung ;
Griffin, Robert G. ;
Dinca, Mircea .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (13) :4923-4928
[3]   Does CO poison Fe-based catalysts for ORR? [J].
Birry, Laurent ;
Zagal, Jose H. ;
Dodelet, Jean-Pol .
ELECTROCHEMISTRY COMMUNICATIONS, 2010, 12 (05) :628-631
[4]   PROJECTOR AUGMENTED-WAVE METHOD [J].
BLOCHL, PE .
PHYSICAL REVIEW B, 1994, 50 (24) :17953-17979
[5]   Transition Metal d-Orbital Splitting Diagrams: An Updated Educational Resource for Square Planar Transition Metal Complexes [J].
Boergel, Jonas ;
Campbell, Michael G. ;
Ritter, Tobias .
JOURNAL OF CHEMICAL EDUCATION, 2016, 93 (01) :118-121
[6]  
Bogdanoff P, 2004, J NEW MAT ELECTR SYS, V7, P85
[7]   Promotion of oxygen reduction by a bio-inspired tethered iron phthalocyanine carbon nanotube-based catalyst [J].
Cao, Ruiguo ;
Thapa, Ranjit ;
Kim, Hyejung ;
Xu, Xiaodong ;
Kim, Min Gyu ;
Li, Qing ;
Park, Noejung ;
Liu, Meilin ;
Cho, Jaephil .
NATURE COMMUNICATIONS, 2013, 4
[8]   Electrodes modified by electrodeposition of CoTAA complexes as selective oxygen cathodes in a direct methanol fuel cell [J].
Convert, P ;
Coutanceau, C ;
Crouïgneau, P ;
Gloaguen, F ;
Lamy, C .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2001, 31 (09) :945-952
[9]   Porous, crystalline, covalent organic frameworks [J].
Côté, AP ;
Benin, AI ;
Ockwig, NW ;
O'Keeffe, M ;
Matzger, AJ ;
Yaghi, OM .
SCIENCE, 2005, 310 (5751) :1166-1170
[10]   Covalent organic frameworks (COFs): from design to applications [J].
Ding, San-Yuan ;
Wang, Wei .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (02) :548-568