阳极
硼氢化
钴
催化作用
材料科学
燃料电池
化学工程
化学
冶金
电极
工程类
有机化学
物理化学
作者
Dafeng Zhang,Bingjie Xue,Fengge Wang,Hao Liang,Yage Cao,Dongliang Zhang,Baozhong Liu
标识
DOI:10.1021/acsanm.4c01074
摘要
Direct borohydride fuel cells require highly efficient and cost-effective electrocatalysts for the borohydride oxidation reaction (BOR) on the anode. This study presents a simple electrodeposition method for directly producing metallic Co nanoflake arrays (Co NAs) on different conductive substrates. The Co NAs synthesized exhibit an open structure and a strong adhesion to the substrates, providing more abundant active sites and thereby being able to facilitate the mass and charge transfer kinetics of BOR. The Co NAs demonstrate excellent catalytic performance for the BOR without the use of noble metals. An impressive current density of up to 726 mA cm–2 at 0.65 V (vs reversible hydrogen electrode) was achieved, which is 5.3 and 2.5 times higher than that of regular Co nanoparticles and commercial Pt/C materials, respectively. In addition, the as-synthesized Co NAs were further successfully employed as the anodic catalyst in a fully liquid-fed NaBH4/H2O2 fuel cell, resulting in a remarkable peak power density of 262.7 mW cm–2 at approximately 0.95 V and an open-circuit cell voltage of 1.83 V. This performance distinctly surpassed that of cells equipped with the control Pt/C electrode and is comparable to recent top-tier results in the field.
科研通智能强力驱动
Strongly Powered by AbleSci AI