Carbon Hollow Fiber Penetration Electrode with Unsaturated Ni‐N 2 Coordination for Enhanced CO 2 Electroreduction
Year: 2025
Type: article
Abstract: Hollow fiber gas penetration electrodes with a compact hierarchical pore structure have emerged as promising platforms for CO 2 electroreduction. However, developing carbon hollow fiber electrodes with efficient CO 2 electrocatalytic performance remains unexplored and challenging. Herein, a straightforward strategy is presented to fabricate robust, self‐standing carbon hollow fiber electrodes modified with an unsaturated Ni‐N 2 coordination structure. This unique hollow fiber electrode configuration effectively enhances the kinetics of CO 2 electro‐conversion to CO. Both density functional theory (DFT) calculations and experimental studies reveal that the Ni‐N 2 structure significantly boosts electrocatalytic activity for CO 2 reduction by reducing the energy barrier for the key intermediate COOH* formation. Consequently, the electrode with unsaturated Ni‐N 2 coordination realizes a high CO Faradaic efficiency (FE) (>90%) as well as a partial current density of 61 mA cm −2 , much superior to those of saturated Ni‐N 4 coordination. In particular, this high performance maintains an exceptional durability for over 100 h, outperforming previously reported carbon supporting electrodes featuring Ni‐N‐C sites. This work opens new avenues for designing advanced carbon electrode structures with enhanced selectivity and activity for CO 2 reduction.
Source: Advanced Science
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $6,730
Funders: National Natural Science Foundation of China, Chinese Academy of Sciences, Ministry of Science and Technology of the People's Republic of China, Science and Technology Commission of Shanghai Municipality, Youth Innovation Promotion Association of the Chinese Academy of Sciences, Youth Innovation Promotion Association, Science and Technology Innovation Plan Of Shanghai Science and Technology Commission, Shanghai Advanced Research Institute, Chinese Academy of Sciences
OpenAlex ID: W4410517690
