Coffee-Waste Templating of Metal Ion-Substituted Cobalt Oxides for the Oxygen Evolution Reaction

被引:39
作者
Yu, Mingquan [1 ]
Chan, Candace K. [2 ]
Tueysuez, Harun [1 ]
机构
[1] Max Planck Inst Kohlenforsch, Kaiser Wilhelm Pl 1, D-45470 Mulheim, Germany
[2] Arizona State Univ, Sch Engn Matter Transport & Energy, Mat Sci & Engn, Tempe, AZ 85287 USA
关键词
cobalt; electrocatalysis; nanostructures; oxygen evolution reaction; waste valorization; WATER-OXIDATION CATALYSIS; EFFICIENT; CO3O4; ELECTROCATALYSTS; NANOPARTICLES; MANGANESE; ELECTROLYSIS; CHALLENGES; ELECTRODES; MECHANISM;
D O I
10.1002/cssc.201701877
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile and scalable method using coffee waste grounds as a hard template has been developed to fabricate nanostructured Co3O4 for the oxygen evolution reaction (OER). Co3O4 incorporating metals with different valences (M/Co=1:4; M=Cu, Ni, Fe, Cr, and W) were also prepared with similar sheet-like structures comprising nanosized crystallites. After detailed characterization by X-ray diffraction, electron microscopy, and nitrogen sorption, the oxides were employed as OER electrocatalysts. Substitution of octahedral and tetrahedral sites of the spinel structure with divalent and trivalent transition metals (Cu, Ni, Fe, and Cr) increased the activity of Co3O4 for the OER, whereas incorporation of hexavalent W led to formation of a second crystal phase and significantly higher electrocatalytic performance. Furthermore, this method is easily scaled up for mass production of Co3O4 with the same nanostructure, which is highly desirable for large-scale application.
引用
收藏
页码:605 / 611
页数:7
相关论文
共 55 条
[1]   Electrochemically induced surface modifications of mesoporous spinets (Co3O4-δ, MnCo2O4-δ, NiCo2O4-δ) as the origin of the OER activity and stability in alkaline medium [J].
Abidat, I. ;
Bouchenafa-Saib, N. ;
Habrioux, A. ;
Comminges, C. ;
Canaff, C. ;
Rousseau, J. ;
Napporn, T. W. ;
Dambournet, D. ;
Borkiewicz, O. ;
Kokoh, K. B. .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (33) :17433-17444
[2]  
[Anonymous], 2017, ANGEW CHEM INT EDIT
[3]  
AXS B., 2014, TOPAS V5 GEN PROFILE
[4]   Theoretical Investigation of the Activity of Cobalt Oxides for the Electrochemical Oxidation of Water [J].
Bajdich, Michal ;
Garcia-Mota, Monica ;
Vojvodic, Aleksandra ;
Norskov, Jens K. ;
Bell, Alexis T. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (36) :13521-13530
[5]   Co3O4 Nanoparticle Water-Oxidation Catalysts Made by Pulsed-Laser Ablation in Liquids [J].
Blakemore, James D. ;
Gray, Harry B. ;
Winkler, Jay R. ;
Mueller, Astrid M. .
ACS CATALYSIS, 2013, 3 (11) :2497-2500
[6]   ELECTROCHEMICAL SURFACE-PROPERTIES OF CO3O4 ELECTRODES [J].
BOGGIO, R ;
CARUGATI, A ;
TRASATTI, S .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1987, 17 (04) :828-840
[7]   Electrosynthesis of Highly Transparent Cobalt Oxide Water Oxidation Catalyst Films from Cobalt Aminopolycarboxylate Complexes [J].
Bonke, Shannon A. ;
Wiechen, Mathias ;
Hocking, Rosalie K. ;
Fang, Xi-Ya ;
Lupton, David W. ;
MacFarlane, Douglas R. ;
Spiccia, Leone .
CHEMSUSCHEM, 2015, 8 (08) :1394-1403
[8]   Cobalt-Iron (Oxy)hydroxide Oxygen Evolution Electrocatalysts: The Role of Structure and Composition on Activity, Stability, and Mechanism [J].
Burke, Michaela S. ;
Kast, Matthew G. ;
Trotochaud, Lena ;
Smith, Adam M. ;
Boettcher, Shannon W. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (10) :3638-3648
[9]   Whole-profile structure solution from powder diffraction data using simulated annealing [J].
Coelho, AA .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2000, 33 (02) :899-908
[10]   The Mechanism of Water Oxidation: From Electrolysis via Homogeneous to Biological Catalysis [J].
Dau, Holger ;
Limberg, Christian ;
Reier, Tobias ;
Risch, Marcel ;
Roggan, Stefan ;
Strasser, Peter .
CHEMCATCHEM, 2010, 2 (07) :724-761