4.8 Article

Interfacial Engineering Enhances the Electroactivity of Frame-Like Concave RhCu Bimetallic Nanocubes for Nitrate Reduction

期刊

ADVANCED ENERGY MATERIALS
卷 12, 期 15, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202103916

关键词

ammonia; bimetallic nanocubes; interfacial engineering; nitrate reduction reaction; RhCu alloys

资金

  1. National Natural Science Foundation of China [21875133, 51873100]
  2. Natural Science Foundation of Shaanxi Province [2020JZ-23]
  3. Fundamental Research Funds for the Central Universities [GK202101005, GK202103062]
  4. Open Foundation of Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured Materials at Guangxi University [2021GXYSOF02]
  5. 111 Project [B14041]

向作者/读者索取更多资源

Polyallylamine-functionalized RhCu bimetallic nanocubes show remarkable performance as an electrocatalyst for the reduction of nitrate to ammonia. The study suggests a potential avenue for constructing advanced catalysts based on organic molecule-mediated interfacial engineering.
Ammonia is a crucial chemical in agriculture, industry, and emerging energy industries, so high-efficient, energy-saving, sustainable, and environmentally-friendly NH3 synthesis strategies are highly desired. Here polyallylamine (PA) functionalized frame-like concave RhCu bimetallic nanocubes (PA-RhCu cNCs) are reported with an electrochemically active surface area of 72.8 m(2) g(-1) as a robust electrocatalyst for the 8e reduction of nitrate (NO3-) to NH3. PA-RhCu cNCs show a remarkable NH3 production yield of 2.40 mg h(-1) mg(cat)(-1) and a high faradaic efficiency of 93.7% at +0.05 V potential. Density functional theory calculations and experimental results indicate that Cu and PA (adsorbed amino) coregulate the Rh d-band center, which slightly weakens the adsorption energy of reaction-related species on Rh. In addition, the electrochemical interface mass transfer accelerated by the surface PA further determines the notable performance of PA-RhCu cNCs for electroreduction of NO3- to NH3. These findings may open an avenue to construct other advanced catalysts based on organic molecule-mediated interfacial engineering in various catalysis/electrocatalysis fields.

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