Chinese Journal of Applied Chemistry ›› 2025, Vol. 42 ›› Issue (7): 901-913.DOI: 10.19894/j.issn.1000-0518.250089
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Zi-Shan HAN, Kang ZOU, Xue YANG(
)
Received:2025-03-04
Accepted:2025-06-19
Published:2025-07-01
Online:2025-07-23
Contact:
Xue YANG
About author:yangx.ripp@sinopec.comSupported by:CLC Number:
Zi-Shan HAN, Kang ZOU, Xue YANG. Research Progress on Triple-Phase Interface Engineering in Electrocatalytic CO2 Reduction Reaction[J]. Chinese Journal of Applied Chemistry, 2025, 42(7): 901-913.
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URL: http://yyhx.ciac.jl.cn/EN/10.19894/j.issn.1000-0518.250089
Fig.2 (A) Schematic picture of the constructed solid-liquid-gas TPI by dispersing PTFE nanoparticles inside the catalyst layer[20]; (B) Schematic illustration of three interfacial states represented by Au/C-F (Cassie state, top), Au/C-P-0.5 (Cassie-Wenzel state, middle) and Au/C-P-2.5 (Wenzel state, bottom) catalyst, respectively[21]; (C) Hydrophilic and hydrophobic characteristics of PFSA ionomers[23]
Fig.3 (A) v-OH vibrational region of H2O without (left) and with (right) CTAB[26]; (B) Schematics of interfacial microenvironment regulation of IPN-PFSA heterogeneous catalyst adlayer[29]
Fig.4 (A) Schematic of an all-metal gas diffusion enhanced Cu electrode[33]; (B) Modelled CO2 volume fraction in the pore body and the pore throat of carbon fabrics[34]
Fig.5 Calculated composition of water flux on the cathode side at different gas flow rates for (A) wet CO2 feeds and (B) dry CO2 feeds[41]; (C) The excess flux of water at cathode and (D) the CO faradaic efficiencies of low water uptake membranes with different thicknesses[43]
Fig.6 (A) Carbonate migration occurs during cell operation at the regeneration voltage[54]; (B) Schematic of a BPM electrode assembly in reverse-bias configuration[55]
Fig.7 (A) Schematic picture showing graphene could act as a protective barrier of the CuNCs after polarization[65]; (B) Calculated Cu+/Cu0 ratio as a function of reaction time at -0.61 V(vs.RHE)[66]
| Product | Conventional process | Conventional unit cost (USD/ton) | CO2RR cost (USD/ton) | Outlook |
|---|---|---|---|---|
| Carbon monoxide (CO)[ | Steam methane reforming, partial oxidation of methane | 150~600 | 200~600 | Near commercial viability; Competitive with some conventional processes |
| Formic acid (HCOOH)[ | Methanol carbonylation, hydrolysis of methyl formate | 200~600 | 550~1 200 | Requires improved catalyst stability and energy efficiency |
| Ethylene (C2H4)[ | Naphtha steam cracking | 600~1 300 | 2 300~7 000 | High cost limits short-term viability; Long-term potential depends on scale and policy support (e.g., carbon pricing) |
| Ethanol (C2H5OH)[ | Biological fermentation, ethylene hydration | 600~1 000 | 1 600~4 500 | Currently costly; Tandem CO pathways may reduce costs over time |
Table 1 Cost comparison of primary products in CO2 electroreduction versus conventional process pathways
| Product | Conventional process | Conventional unit cost (USD/ton) | CO2RR cost (USD/ton) | Outlook |
|---|---|---|---|---|
| Carbon monoxide (CO)[ | Steam methane reforming, partial oxidation of methane | 150~600 | 200~600 | Near commercial viability; Competitive with some conventional processes |
| Formic acid (HCOOH)[ | Methanol carbonylation, hydrolysis of methyl formate | 200~600 | 550~1 200 | Requires improved catalyst stability and energy efficiency |
| Ethylene (C2H4)[ | Naphtha steam cracking | 600~1 300 | 2 300~7 000 | High cost limits short-term viability; Long-term potential depends on scale and policy support (e.g., carbon pricing) |
| Ethanol (C2H5OH)[ | Biological fermentation, ethylene hydration | 600~1 000 | 1 600~4 500 | Currently costly; Tandem CO pathways may reduce costs over time |
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