Urea synthesis by Plasmon-Assisted N2 and CO2 co-electrolysis onto heterojunctions decorated with silver nanoparticles

IF 13.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL
Leandro A. Faustino, Leonardo D. de Angelis, Eduardo C. de Melo, Giliandro Farias, Egon C. dos Santos, Caetano R. Miranda, Ana G. Buzanich, Roberto M. Torresi, Paulo F.M. de Oliveira, Susana I. Cordoba de Torresi
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Abstract

The N2 + CO2 co-electrolysis to urea synthesis has become a promising alternative to the energy intensive traditional processes for urea production. However, there are still challenges in this approach, especially due to the competition with HER (Hydrogen Evolution Reaction) leading to low efficiency. Electrochemistry assisted by localized surface plasmon resonance (LSPR) using metal nanoparticles has been reported to enhance different electrochemical reactions. Here we report an electrochemical LSPR assisted urea synthesis using Ag nanoparticles (NPs) supported on BiVO4/BiFeO3 catalyst mechanochemically synthesized. The electrochemical experiments were performed under dark and upon plasmon excitation at the LSPR region of Ag NPs. Our results demonstrated that exciting in the LSPR range, urea yield rate and Faradic efficiency were considerably improved with reduced overpotential, 19.2μmol h−1 g−1 and FE 24.4 % at + 0.1 V vs RHE compared to 9.6μmol h−1 g−1 and FE 9.4 % at −0.2 V vs RHE under dark conditions. Further in situ FTIR-RAS experiments for mechanism investigation revealed the presence of N-H and C-N intermediates and the real effect of Ag plasmon excitation on HER and N2 + CO2 co-electrolysis. Theoretical calculations confirm the energy of the species involved in C-N coupling as well the role of the complex catalytic sites, which agrees with XAS measurements.

Abstract Image

等离子体辅助N2和CO2共电解在银纳米粒子修饰异质结上合成尿素
N2 + CO2共电解合成尿素已成为替代传统高能耗尿素生产工艺的一种很有前景的方法。然而,这种方法仍然存在挑战,特别是由于与HER(析氢反应)的竞争导致效率低下。利用金属纳米粒子在局部表面等离子体共振(LSPR)辅助下的电化学可以增强不同的电化学反应。本文报道了一种电化学LSPR辅助尿素合成方法,该方法采用机械化学方法合成了BiVO4/BiFeO3催化剂负载的银纳米颗粒(NPs)。在银纳米粒子LSPR区分别进行了暗激发和等离子激元激发下的电化学实验。我们的研究结果表明,在LSPR范围内,在 + 0.1 V / RHE条件下,过电位降低19.2μmol h−1 g−1,FE降低24.4 %,尿素收率和Faradic效率显著提高,而在- 0.2 V / RHE条件下,过电位降低9.6μmol h−1 g−1,FE降低9.4 %。进一步的原位FTIR-RAS实验揭示了N-H和C-N中间体的存在以及银等离子激元激发对HER和N2 + CO2共电解的真实影响。理论计算证实了参与C-N耦合的物质的能量以及复合催化位点的作用,这与XAS测量结果一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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