Highly Scalable Conversion of Blood Protoporphyrin to Efficient Electrocatalyst for CO2-to-CO Conversion

被引:8
|
作者
Miola, Matteo [1 ]
Li, Simin [2 ]
Hu, Xin-Ming [3 ]
Ceccato, Marcel [2 ]
Surkus, Annette-E. [4 ]
Welter, Edmund [5 ]
Pedersen, Steen U. [2 ]
Junge, Henrik [4 ]
Skrydstrup, Troels [6 ]
Beller, Matthias [4 ]
Daasbjerg, Kim [2 ]
机构
[1] Univ Groningen, Engn & Technol Inst Groningen, Chem Engn Grp, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
[2] Aarhus Univ, Dept Chem, Langelandsgade 140, DK-8000 Aarhus, Denmark
[3] Shandong Univ, Environm Res Inst, Binhai Rd 72, Qingdao 266237, Peoples R China
[4] Leibniz Inst Katalyse, Albert Einstein Str 29a, D-18059 Rostock, Germany
[5] DESY, Notkestr 85, D-22607 Hamburg, Germany
[6] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, Carbon Dioxide Activat Ctr CADIAC, Gustav Wields Vej 14, DK-8000 Aarhus, Denmark
基金
新加坡国家研究基金会;
关键词
CO; (2) reduction; heat treatment; heterogeneous electrocatalysis; molecular catalyst; structure‐ activity relationship; CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; SYNTHETIC STRATEGIES; CO2; REDUCTION; HEMIN; CATALYSTS; METAL; IMMOBILIZATION; NANOTUBES; PORPHYRIN;
D O I
10.1002/admi.202100067
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical CO2 reduction to valuable chemicals represents a green and sustainable approach to close the anthropogenic carbon cycle, but has been impeded by low efficiency and high cost of electrocatalysts. Here, a cost-effective hybrid catalyst consisting of hemin (chloroprotoporphyrin IX iron(III)), a product recovered from bovine blood, adsorbed onto commercial Vulcan carbon is reported. Upon heat treatment, this material shows significantly improved activity and selectivity for CO2 reduction in water while exhibiting good stability for more than 10 h. The heat treatment leads to consecutive removal of the axial chlorine atom and decomposition of the iron porphyrin ring, restructuring to form atomic Fe sites. The optimized hybrid catalyst obtained at 900 degrees C shows near-unity selectivity for reduction of CO2 to CO at a small overpotential of 310 mV. The insight into transformation of adsorbed Fe complexes into single Fe atoms upon heat treatment provides guidance for development of single atom catalysts.
引用
收藏
页数:9
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