Facile Synthesis of Carbon Nanobelts Decorated with Cu and Pd for Nitrate Electroreduction to Ammonia

电催化剂 材料科学 可逆氢电极 催化作用 硝酸盐 氨生产 无机化学 纳米团簇 亚硝酸盐 碳纤维 产量(工程) 法拉第效率 电化学 电极 化学 纳米技术 有机化学 复合数 冶金 工作电极 物理化学 复合材料
作者
Zhe Wang,Congcong Sun,Xiaoxia Bai,Zhenni Wang,Xin Yu,Xin Tong,Zheng Wang,Hui Zhang,Haili Pang,Lijun Zhou,Weiwei Wu,Yanping Liang,Ajit Khosla,Zhenhuan Zhao
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (27): 30969-30978 被引量:53
标识
DOI:10.1021/acsami.2c09357
摘要

The electrocatalytic nitrate conversion of ammonia at ambient conditions provides not only a solution for restoring the imbalance in the global nitrogen cycle but also a sustainable alternative for the Haber-Bosch process. However, large-scale and efficient application of electrocatalytic denitrification has been limited by the lack of active catalysts with a high selectivity of nitrate reduction to N2. In this work, we present a one-step solution processed synthetic strategy at low temperature to prepare carbon-nanobelts-supported uniform Cu and Pd nanoclusters. It is found that Cu catalyzed the formation of carbon nanobelts. The prepared samples were used for the green synthesis of ammonia from nitrate by electrocatalysis. For the nitrate reduction reaction (NO3RR), Cu-Pd/C nanobelts show higher activity than Cu/C nanobelts, achieving a high yield of ammonia of 220.8 μg mgcat-1 h-1 with a Faradaic efficiency (FE) of 62.3% at -0.4 V vs RHE (reversible hydrogen electrode), while for the nitrite reduction reaction (NO2RR), a high FE of 95% at -0.2 V vs RHE can be obtained for Cu/C nanobelts with the yield of ammonia increased with the negative shift of the applied potentials. Theoretical calculations demonstrated that Pd and Cu are responsible for hydrogen evolution reaction (HER) and NO3RR, respectively.

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