电催化剂
氧还原反应
硝酸盐
多孔性
材料科学
对偶(语法数字)
还原(数学)
纳米结构
催化作用
氢
化学工程
化学
无机化学
纳米技术
电极
电化学
复合材料
物理化学
有机化学
数学
艺术
工程类
文学类
几何学
作者
Dasari Sai Hemanth Kumar,Manzoor Ahmad Pandit,Vinay Kumar Kolakaluri,Krishnamurthi Muralidharan
标识
DOI:10.1016/j.jes.2025.04.070
摘要
The potential to eliminate nitrate pollution in waste effluents by electrochemically reducing nitrate to ammonia has sparked global interest in developing highly active electrocatalysts for the nitrate reduction reaction (NO3RR). Metal-organic frameworks (MOFs) have emerged as a promising candidate for creating the next-generation NO3RR electrocatalysts due to their abundant active metal sites, electrical conductivity, and well-organized porous structure. In this context, we report the synthesis and applications of a unique bimetallic MOF, i.e., CuFe(x:y)MOF, as an efficient dual electrocatalyst for NO3RR and hydrogen evolution reaction (HER). We have carefully adjusted the Cu to Fe ratio in CuFe(x:y)MOF to achieve the best possible result. The CuFe(1:2)MOF, with its distinct features, showed excellent NO3RR with a high ammonia yield of 5.08 mmol/(h⋅cm2) and 87 % faradaic efficiency. Moreover, the material demonstrated catalytic activity for the hydrogen evolution reaction, exhibiting an overpotential of 175 mV and a low Tafel slope of 295 mV/dec under optimized conditions. Further, chronoamperometry studies revealed that the catalyst remained stable for 24 h. These findings underscore the potential of the CuFe(x:y)MOF as an efficient dual electrocatalyst and a significant step forward in developing next-generation catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI