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.