Single Iridium Pincer Complex for Roundtrip Electrochemical Conversion between Carbon Dioxide and Formate

被引:15
作者
Bi, Jiaojiao [1 ,3 ]
Hou, Pengfei [1 ,3 ]
Kang, Peng [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, 29 Zhongguancun East Rd, Beijing 100190, Peoples R China
[2] Tianjin Univ, Sch Chem Engn & Technol, 135 Yaguan Rd, Tianjin 300350, Peoples R China
[3] Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China
关键词
Iridium Complex; Pincer Ligand; Carbon Dioxide Reduction; Formate Oxidation; Electrocatalysis; SELECTIVE ELECTROCATALYTIC REDUCTION; HIGH-QUALITY HYDROGEN; FORMIC-ACID; CO2; REDUCTION; PD-AU/C; CATALYST; DECOMPOSITION; MECHANISM; METHANOL; H-2;
D O I
10.1002/cctc.201900083
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
An iridium (III) complex based on a PONOP pincer ligand (PONOP=2,6-bis(di-tert-butylphosphinito)pyridine) is a versatile catalyst for both electro-reduction of CO2 to formate and formate electro-oxidation to CO2. The electro-reduction of CO2 in acetonitrile is very efficient and selective, and the Faradaic efficiency for formate was 97 % and the turnover frequency (TOF) was as high as 67 s(-1). In addition, the complex is an effective electrocatalyst for formate electro-oxidation with apparent TOF of 4.8 s(-1) (0.06 M formate), and CO2 was the sole product. The catalyst was stable for 35 h of electrolysis. It can serve as a single catalyst for the roundtrip conversion between CO2 and formate with potential for electrochemical energy storage. Electrochemical and NMR spectroscopic studies suggested that the hydride species is critical for the bifunctional reactivity.
引用
收藏
页码:2069 / 2072
页数:4
相关论文
共 38 条
[1]   Frontiers, Opportunities, and Challenges in Biochemical and Chemical Catalysis of CO2 Fixation [J].
Appel, Aaron M. ;
Bercaw, John E. ;
Bocarsly, Andrew B. ;
Dobbek, Holger ;
DuBois, Daniel L. ;
Dupuis, Michel ;
Ferry, James G. ;
Fujita, Etsuko ;
Hille, Russ ;
Kenis, Paul J. A. ;
Kerfeld, Cheal A. ;
Morris, Robert H. ;
Peden, Charles H. F. ;
Portis, Archie R. ;
Ragsdale, Stephen W. ;
Rauchfuss, Thomas B. ;
Reek, Joost N. H. ;
Seefeldt, Lance C. ;
Thauer, Rudolf K. ;
Waldrop, Grover L. .
CHEMICAL REVIEWS, 2013, 113 (08) :6621-6658
[2]   Investigations of Iridium-Mediated Reversible C-H Bond Cleavage: Characterization of a 16-Electron Iridium(III) Methyl Hydride Complex [J].
Bernskoetter, Wesley H. ;
Hanson, Susan Kloek ;
Buzak, Sara K. ;
Davis, Zoe ;
White, Peter S. ;
Swartz, Rodney ;
Goldberg, Karen I. ;
Brookhart, Maurice .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (24) :8603-8613
[3]   ELECTROCATALYTIC REDUCTION OF CARBON-DIOXIDE BY 2,2'-BIPYRIDINE COMPLEXES OF RHODIUM AND IRIDIUM [J].
BOLINGER, CM ;
STORY, N ;
SULLIVAN, BP ;
MEYER, TJ .
INORGANIC CHEMISTRY, 1988, 27 (25) :4582-4587
[4]   Theoretical mechanism studies on the electrocatalytic reduction of CO2 to formate by water-stable iridium dihydride pincer complex [J].
Cao, Linlin ;
Sun, Chuanzhi ;
Sun, Nan ;
Meng, Lin ;
Chen, Dezhan .
DALTON TRANSACTIONS, 2013, 42 (16) :5755-5763
[5]   Proton-Assisted Reduction of CO2 by Cobalt Aminopyridine Macrocycles [J].
Chapovetsky, Alon ;
Do, Thomas H. ;
Haiges, Ralf ;
Takase, Michael K. ;
Marinescu, Smaranda C. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (18) :5765-5768
[6]  
Eissen M, 2002, ANGEW CHEM INT EDIT, V41, P414, DOI 10.1002/1521-3773(20020201)41:3<414::AID-ANIE414>3.0.CO
[7]  
2-N
[8]  
Eissen M., 2002, ANGEW CHEM, V114, P402
[9]   Formic Acid as a Hydrogen Energy Carrier [J].
Eppinger, Jorg ;
Huang, Kuo-Wei .
ACS ENERGY LETTERS, 2017, 2 (01) :188-195
[10]   Electrocatalytic Oxidation of Formate by [Ni(PR2NR′2)2(CH3CN)]2+ Complexes [J].
Galan, Brandon R. ;
Schoeffel, Julia ;
Linehan, John C. ;
Seu, Candace ;
Appel, Aaron M. ;
Roberts, John A. S. ;
Helm, Monte L. ;
Kilgore, Uriah J. ;
Yang, Jenny Y. ;
DuBois, Daniel L. ;
Kubiak, Clifford P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (32) :12767-12779