Electrochemical carbon dioxide (CO2) reduction can in principle convert carbon emissions to fuels and value-added chemicals, such as hydrocarbons and alcohols, using renewable energy, but the efficiency of the process is limited by its sluggish kinetics1,2. Molecular catalysts have well defined active sites and accurately tailorable structures that allow mechanism-based performance optimization, and transition-metal complexes have been extensively explored in this regard. However, these catalysts generally lack the ability to promote CO2 reduction beyond the two-electron process to generate more valuable products1,3. Here we show that when immobilized on carbon nanotubes, cobalt phthalocyanine—used previously to reduce CO2 to primarily CO—catalyses the six-electron reduction of CO2 to methanol with appreciable activity and selectivity. We find that the conversion, which proceeds via a distinct domino process with CO as an intermediate, generates methanol with a Faradaic efficiency higher than 40 per cent and a partial current density greater than 10 milliamperes per square centimetre at −0.94 volts with respect to the reversible hydrogen electrode in a near-neutral electrolyte. The catalytic activity decreases over time owing to the detrimental reduction of the phthalocyanine ligand, which can be suppressed by appending electron-donating amino substituents to the phthalocyanine ring. The improved molecule-based electrocatalyst converts CO2 to methanol with considerable activity and selectivity and with stable performance over at least 12 hours.
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Data supporting the findings of this study are available from the corresponding authors upon reasonable request. Source data for Figs. 2, 4 are provided with the paper.
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This work was supported by the US National Science Foundation (grant CHE-1651717). X.L. acknowledges a Croucher Fellowship for Postdoctoral Research. Z.J. and Y.L. acknowledge financial support by Shenzhen fundamental research funding (JCYJ20160608140827794) and the Guangdong Provincial Key Laboratory (2018B030322001). The authors thank Q. Wang and M. Gu (Southern University of Science and Technology) for assistance with STEM imaging.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Peer review information Nature thanks Robert Francke and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Extended data figures and tables
a–d, Potential-dependent catalytic performance of CO2 electroreduction by FePc/CNT (a, b) and NiPc/CNT (c, d).
a, b, Typical gas chromatography diagrams from the flame ionization detector (a) and the thermal conductivity detector (b),showing the presence of CO and H2 (marked in red) and the absence of other common gas products (marked in grey). c, d, Typical 1H NMR (c) and 13C NMR (d) spectra of a liquid sample after CO2 electroreduction electrolysis (green traces) versus a blank 0.1 M KHCO3 solution (red traces). e, f, Representative 1H NMR spectra of liquid samples after 1 h of CO2 reduction electrolysis catalysed by CoPc/CNT at −0.94 V versus RHE (e) and 1 h of CO reduction electrolysis catalysed by CoPc–NH2/CNT at −0.95 V versus RHE (f). The detailed information used to determine the FE of MeOH production is given in the diagrams.
a, b, Potential-dependent product selectivity (a) and partial current density (b) for CO2 electroreduction catalysed by CoPc/CNT under N2.
a, b, Potential-dependent product selectivity (a) and partial current density (b) for the electroreduction of CO2 by bare CoPc aggregates on carbon paper. c, Nyquist plots of bare CoPc, a physical mixture of CoPc and CNTs and the CoPc/CNT hybrid, measured at −0.94 V versus RHE in a 0.1 M aqueous KHCO3 solution saturated with CO2 with a scanning frequency range from 200 kHz to 100 Hz and an a.c. amplitude of 5 mV. Z′ and Z″ refer to the real and imaginary parts of impedance, respectively. The inset shows the enlarged area where the traces for the CoPc/CNT hybrid and the mixture of CoPc and CNTs are clearer. d, Selectivity (FEMeOH) and partial current density (jMeOH) for CO2 reduction to MeOH catalysed by bare CoPc (‘Bare’), the CoPc/CNT physical mixture (‘CNT Mix’), the CoPc/Vulcan XC72 mixture (‘VXC72 Mix’), the CoPc/Ketjenblack mixture (‘KB Mix’) and the CoPc/CNT hybrid (‘CNT Hybrid’) at −0.94 V versus RHE.
a, Gas product selectivity and total current density in a 12-h electrolysis of CO2 reduction catalysed by CoPc/CNT at −0.94 V versus RHE. b, c, SEM images of an as-deposited CoPc/CNT electrode before (b) and after (c) catalysing CO2 reduction electrolysis at −0.94 V versus RHE for 12 h.
UV-Vis spectra of post-electrolysis CoPc and free-base phthalocyanine (H2Pc) in DMF.
a, b, The curves were recorded at a scan rate of 400 mV s−1 in a 0.1 M aqueous KHCO3 solution under N2 (a) and CO2 (b). The most prominent cathodic (ic) and anodic (ia) features of the molecules are labelled. The redox potential of CoPc–NH2/CNT is more negative than that of CoPc/CNT.
Catalytic performance of CoPc–NH2/CNT for electroreduction of CO to MeOH.
a, High-resolution mass spectrometry results for CoPc–NH2. Calculated for CoC32H20N12: 631.12604; found: 631.12435. b, UV-Vis spectrum of CoPc–NH2 in 15 M H2SO4. λmax = 210 nm, 299 nm, 380 nm and 739 nm.
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Wu, Y., Jiang, Z., Lu, X. et al. Domino electroreduction of CO2 to methanol on a molecular catalyst. Nature 575, 639–642 (2019). https://doi.org/10.1038/s41586-019-1760-8
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