In Situ Phase Transformation-Enabled Metal–Organic Frameworks for Efficient CO<sub>2</sub> Electroreduction to Multicarbon Products in Strong Acidic Media

The electrochemical CO2 reduction reaction (CO2RR) has been acknowledged as a promising strategy to relieve carbon emissions by converting CO2 to essential chemicals. Despite significant progresses that have been made in neutral and alkaline media, the implementation of CO2RR in acidic conditions remains challenging due to the harsh conditions, especially in producing high-value multicarbon products. Here, we report that Cu-btca (btca = benzotriazole-5-carboxylic acid) metal–organic framework (MOF) nanostructures can act as a stable catalyst for the CO2RR in an acidic environment. The Cu-btca MOF undergoes phase transformation and morphology evolution during electrolysis, forming a stable porous Cu-btca MOF network. The resultant MOF network exhibits excellent selectivity toward ethylene and multicarbon products with Faradaic efficiencies of 51.2% and 81.9%, respectively, in a strong acidic electrolyte with a flow cell at 300 mA/cm2. Mechanism studies uncover that the Cu-btca MOF network can limit the proton reduction to suppress hydrogen evolution and maintain high local *CO concentration to promote CO2RR. Theoretical calculations suggest that two adjacent Cu sites in the Cu-btca MOF provide a favorable microenvironment for carbon–carbon coupling, facilitating the multicarbon production. This work reveals that rational structure control of MOFs can enable highly selective and efficient CO2 electroreduction to multicarbon products in strong acidic conditions toward practical applications.

Authors

Institutions

Publication Details

Journal
ACS Nano
Published
2024-11-22
DOI
https://doi.org/10.1021/acsnano.4c12245
Citations
40
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
Field-Weighted Citation Impact
4.09

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

In Situ Phase Transformation-Enabled Metal–Organic Frameworks for Efficient CO2 Electroreduction to Multicarbon Products in Strong Acidic Media

Chongyi Ling, Zezhong Xie, Jinli Yu, Fengkun Hao et al.
40 citations
ACS Nano
CO2 Reduction Techniques and Catalysts
4.09
article

In Situ Phase Transformation-Enabled Metal–Organic Frameworks for Efficient CO2 Electroreduction to Multicarbon Products in Strong Acidic Media

Chongyi Ling, Zezhong Xie, Jinli Yu, Fengkun Hao, Yi Wang, Yunhao Wang, Kun Wang, Zhanxi Fan, Jingying Sun, Shuqin Song, Jingwen Zhou, Guozhi Wang, Yangbo Ma, Zonglong Zhu, Pengyi Lu, Qiang Li, Xiang Meng, Liang Guo, Juan Xiao
article en
40 citations

Abstract

The electrochemical CO2 reduction reaction (CO2RR) has been acknowledged as a promising strategy to relieve carbon emissions by converting CO2 to essential chemicals. Despite significant progresses that have been made in neutral and alkaline media, the implementation of CO2RR in acidic conditions remains challenging due to the harsh conditions, especially in producing high-value multicarbon products. Here, we report that Cu-btca (btca = benzotriazole-5-carboxylic acid) metal–organic framework (MOF) nanostructures can act as a stable catalyst for the CO2RR in an acidic environment. The Cu-btca MOF undergoes phase transformation and morphology evolution during electrolysis, forming a stable porous Cu-btca MOF network. The resultant MOF network exhibits excellent selectivity toward ethylene and multicarbon products with Faradaic efficiencies of 51.2% and 81.9%, respectively, in a strong acidic electrolyte with a flow cell at 300 mA/cm2. Mechanism studies uncover that the Cu-btca MOF network can limit the proton reduction to suppress hydrogen evolution and maintain high local *CO concentration to promote CO2RR. Theoretical calculations suggest that two adjacent Cu sites in the Cu-btca MOF provide a favorable microenvironment for carbon–carbon coupling, facilitating the multicarbon production. This work reveals that rational structure control of MOFs can enable highly selective and efficient CO2 electroreduction to multicarbon products in strong acidic conditions toward practical applications.

ACS NanoVol. 18(49)
Sun Yat-sen University (CN), City University of Hong Kong (HK), City University of Hong Kong, Shenzhen Research Institute (CN), Southeast University (CN)
City University of Hong Kong, Science and Technology Foundation of Shenzhen City, National Natural Science Foundation of China, Research Grants Council, University Grants Committee, Guangdong Key Laboratory of Fuel Cell Technology, Key Technologies Research and Development Program of Guangzhou, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 5%
CO2 Reduction Techniques and Catalysts
4.09
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.