纳米团簇
催化作用
选择性
材料科学
氨
电化学
硝酸盐
无机化学
选择性还原
化学工程
纳米技术
化学
电极
物理化学
有机化学
工程类
作者
Yunqing Zhu,Gaigai Dong,Fan Pan,Tian Wang,Linbo Zhang,Hanlin Wang,Linke Ge,Peng Zhang
标识
DOI:10.1021/acsami.5c01200
摘要
In this study, Ir nanoclusters adorned with abundant p-mercaptobenzoic acid (p-MBA) ligands were employed to fabricate an electrocatalytic material consisting of Ir nanoclusters embedded within two-dimensional Co-MOF nanosheets (Ir NCs@Co-MOF) for the electrocatalytic NO3- reduction reaction (NO3-RR). TEM analysis confirmed that Ir nanoclusters are uniformly distributed in 2D Co-MOF nanosheets, with an average diameter of about 1.8 nm. At a potential of -0.8 V vs RHE, the Ir NCs@Co-MOF catalyst achieved a nitrate conversion rate, ammonia selectivity, and yield of 92.5, 81.4%, and 230.1 μg·h-1·cm-2, respectively, over a reaction duration of 120 min. The strong interaction between Ir nanoclusters and Co-MOF serves to enhance electrocatalytic activity and accelerate the rate of nitrate reduction. Stability tests indicated that after 20 cycles, both the nitrate conversion and ammonia selectivity of the Ir NCs@Co-MOF catalyst demonstrated relative stability, thereby indicating a robust performance for this catalytic system. The results of EPR and TBA quenching experiments indicate that *H plays a key role in the NO3-RR process. In situ DEMS investigations revealed that during the NO3-RR process, the reaction pathway was as follows: *NO3 → *NO2 → *NO → *NOH → *NH2OH → *NH2 → *NH3 → NH3.
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