Electroreduction of Carbon Dioxide by Heterogenized Cofacial Porphyrins

Pengfei Tian , Jianjun Su , Yun Song , Ruquan Ye , Minghui Zhu

Transactions of Tianjin University ›› 2022, Vol. 28 ›› Issue (1) : 73 -79.

PDF
Transactions of Tianjin University ›› 2022, Vol. 28 ›› Issue (1) : 73 -79. DOI: 10.1007/s12209-021-00305-8
Research Article

Electroreduction of Carbon Dioxide by Heterogenized Cofacial Porphyrins

Author information +
History +
PDF

Abstract

Great attention has been paid to cofacial porphyrins due to their many unique advantages over their monomeric analogs. However, their synthesis is usually complicated. In this work, a facile impregnation method for preparing heterogenized, cofacially stacked porphyrins is proposed. An anionic porphyrin is introduced as an underlayer for immobilization of cationic cobalt porphyrin via electrostatic force. The metal center of the underlying molecule contributes to the electronic structure of the upper cationic cobalt porphyrin. Screening reveals the anionic iron porphyrin to be the most efficient underlayer molecule, lowering the activation energy barrier of CO2 electroreduction, with an improved turnover frequency by 74% to 8.0 s−1 at − 0.6 V versus RHE.

Keywords

CO2RR / Porphyrin / Cofacial / Heterogenization

Cite this article

Download citation ▾
Pengfei Tian, Jianjun Su, Yun Song, Ruquan Ye, Minghui Zhu. Electroreduction of Carbon Dioxide by Heterogenized Cofacial Porphyrins. Transactions of Tianjin University, 2022, 28(1): 73-79 DOI:10.1007/s12209-021-00305-8

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Manbeck GF, Fujita E A review of iron and cobalt porphyrins, phthalocyanines and related complexes for electrochemical and photochemical reduction of carbon dioxide. J Porphyrins Phthalocyanines, 2015, 19(1–3): 45-64.

[2]

Sun CF, Gobetto R, Nervi C Recent advances in catalytic CO2 reduction by organometal complexes anchored on modified electrodes. New J Chem, 2016, 40(7): 5656-5661.

[3]

Elouarzaki K, Kannan V, Jose V, et al. Recent trends, benchmarking, and challenges of electrochemical reduction of CO2 by molecular catalysts. Adv Energy Mater, 2019, 9(24): 1900090.

[4]

Birdja YY, Pérez-Gallent E, Figueiredo MC, et al. Advances and challenges in understanding the electrocatalytic conversion of carbon dioxide to fuels. Nat Energy, 2019, 4(9): 732-745.

[5]

Choi J, Kim J, Wagner P, et al. Energy efficient electrochemical reduction of CO2 to CO using a three-dimensional porphyrin/graphene hydrogel. Energy Environ Sci, 2019, 2: 747-755.

[6]

Hu XM, Rønne MH, Pedersen SU, et al. Enhanced catalytic activity of cobalt porphyrin in CO2 electroreduction upon immobilization on carbon materials. Angew Chem Int Ed, 2017, 56(23): 6468-6472.

[7]

Tatin A, Comminges C, Kokoh B, et al. Efficient electrolyzer for CO2 splitting in neutral water using earth-abundant materials. Proc Natl Acad Sci, 2016, 113(20): 5526-5529.

[8]

Zion N, Friedman A, Levy N, et al. Bioinspired electrocatalysis of oxygen reduction reaction in fuel cells using molecular catalysts. Adv Mater, 2018, 30(41): 1800406.

[9]

Zhu M, Chen J, Huang L, et al. Covalently grafting cobalt porphyrin onto carbon nanotubes for efficient CO2 electroreduction. Angew Chem Int Ed Engl, 2019, 58(20): 6595-6599.

[10]

Mohamed EA, Zahran ZN, Naruta Y Efficient heterogeneous CO2 to CO conversion with a phosphonic acid fabricated cofacial iron porphyrin dimer. Chem Mater, 2017, 29(17): 7140-7150.

[11]

Guilard R, Brandes S, Tardieux C, et al. Synthesis and characterization of cofacial metallodiporphyrins involving cobalt and Lewis acid metals: new dinuclear multielectron redox catalysts of dioxygen reduction. J Am Chem Soc, 1995, 117(47): 11721-11729.

[12]

Peljo P, Murtomäki L, Kallio T, et al. Biomimetic oxygen reduction by cofacial porphyrins at a liquid-liquid interface. J Am Chem Soc, 2012, 134(13): 5974-5984.

[13]

Takai A, Gros CP, Barbe JM, et al. Enhanced electron-transfer properties of cofacial porphyrin dimers through π–π interactions. Chemistry, 2009, 15(13): 3110-3122.

[14]

Collman JP, Kim K, Leidner CR Synthesis, characterization, and electrochemistry of novel diruthenium cofacial porphyrin dimers. Inorg Chem, 1987, 26(7): 1152-1157.

[15]

Oldacre AN, Friedman AE, Cook TR A self-assembled cofacial cobalt porphyrin prism for oxygen reduction catalysis. J Am Chem Soc, 2017, 139(4): 1424-1427.

[16]

Collman JP, Denisevich P, Konai Y, et al. Electrode catalysis of the four-electron reduction of oxygen to water by dicobalt face-to-face porphyrins. J Am Chem Soc, 1980, 102(19): 6027-6036.

[17]

Collman JP, Bencosme CS, Durand RR Jr, et al. Mixed-metal face-to-face porphyrin dimers. J Am Chem Soc, 1983, 105(9): 2699-2703.

[18]

Durand RR, Bencosme CS, Collman JP, et al. Mechanistic aspects of the catalytic reduction of dioxygen by cofacial metalloporphyrins. J Am Chem Soc, 1983, 105(9): 2710-2718.

[19]

Nakamura T, Ube H, Shionoya M Silver-mediated formation of a cofacial porphyrin dimer with the ability to intercalate aromatic molecules. Angew Chem Int Ed Engl, 2013, 52(46): 12096-12100.

[20]

Oliveri CG, Heo J, Nguyen ST, et al. A convergent coordination chemistry-based approach to dissymmetric macrocyclic cofacial porphyrin complexes. Inorg Chem, 2007, 46(19): 7716-7718.

[21]

Suijkerbuijk BMJM, Tooke DM, Spek AL, et al. One-dimensional, cofacial porphyrin polymers formed by self-assembly of meso-tetrakis(ERE donor) zinc(II) porphyrins. Chem Asian J, 2007, 2(7): 889-903.

[22]

Hepburn C, Adlen E, Beddington J, et al. The technological and economic prospects for CO2 utilization and removal. Nature, 2019, 575(7781): 87-97.

[23]

Gruber N, Clement D, Carter BR, et al. The oceanic sink for anthropogenic CO2 from 1994 to 2007. Science, 2019, 363(6432): 1193-1199.

[24]

Mohamed EA, Zahran ZN, Naruta Y Efficient electrocatalytic CO2 reduction with a molecular cofacial iron porphyrin dimer. Chem Commun Camb Engl, 2015, 51(95): 16900-16903.

[25]

Zahran ZN, Mohamed EA, Naruta Y Bio-inspired cofacial Fe porphyrin dimers for efficient electrocatalytic CO2 to CO conversion: overpotential tuning by substituents at the porphyrin rings. Sci Rep, 2016, 6: 24533.

[26]

Smith PT, Benke BP, Cao Z, et al. Iron porphyrins embedded into a supramolecular porous organic cage for electrochemical CO2 reduction in water. Angew Chem, 2018, 130(31): 9832-9836.

[27]

Zhu MH, Yang DT, Ye RQ, et al. Inductive and electrostatic effects on cobalt porphyrins for heterogeneous electrocatalytic carbon dioxide reduction. Catal Sci Technol, 2019, 9(4): 974-980.

[28]

Adamo C, Barone V Toward reliable density functional methods without adjustable parameters: the PBE0 model. J Chem Phys, 1999, 110(13): 6158-6170.

[29]

Hay PJ, Wadt WR Ab initio effective core potentials for molecular calculations: potentials for the transition metal atoms Sc to Hg. J Chem Phys, 1985, 82(1): 270-283.

[30]

Wadt WR, Hay PJ Ab initio effective core potentials for molecular calculations: potentials for main group elements Na to Bi. J Chem Phys, 1985, 82(1): 284-298.

[31]

Hay PJ, Wadt WR Ab initio effective core potentials for molecular calculations: potentials for K to Au including the outermost core orbitals. J Chem Phys, 1985, 82(1): 299-310.

[32]

Lin S, Diercks CS, Zhang YB, et al. Covalent organic frameworks comprising cobalt porphyrins for catalytic CO2 reduction in water. Science, 2015, 349(6253): 1208-1213.

[33]

Costentin C, Drouet S, Robert M, et al. A local proton source enhances CO2 electroreduction to CO by a molecular Fe catalyst. Science, 2012, 338(6103): 90-94.

[34]

Zhu MH, Ye RQ, Jin K, et al. Elucidating the reactivity and mechanism of CO2 electroreduction at highly dispersed cobalt phthalocyanine. ACS Energy Lett, 2018, 3(6): 1381-1386.

AI Summary AI Mindmap
PDF

123

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/