计时安培法
氨
电催化剂
氨生产
催化作用
材料科学
电解
X射线光电子能谱
无机化学
纳米线
电化学
法拉第效率
产量(工程)
硝酸盐
化学工程
扫描电子显微镜
化学
核化学
选择性催化还原
分析化学(期刊)
纳米颗粒
作者
Kauan L. Gomes,Manuel E. G. Winkler,Matheus P. Sales,João Batista Souza,Juliano Alves Bonacin,Raphael Nagao
标识
DOI:10.1021/acsaem.5c02502
摘要
The electrochemical nitrate reduction reaction (NO3RR) offers a sustainable alternative for ammonia synthesis under mild conditions, addressing both nitrate pollution and the energy-intensive nature of the Haber–Bosch process. In this work, Co3O4 nanowires supported on TiO2/Ti were synthesized and evaluated for NO3RR in an H-type electrochemical cell using Ar-saturated 1.0 mol L–1 NaOH containing 20 mmol L–1 NaNO3. After confirming NO3RR activity via cyclic voltammetry, 1 h chronoamperometry was performed at potentials ranging from 0 to −0.4 V vs RHE (in 100 mV steps). The catalyst exhibited ammonia production at 0.0 V vs RHE, achieving a maximum faradaic efficiency (FE) of 80.0 ± 5.8% at −0.3 V vs RHE and a maximum yield rate (YR) of 93.3 ± 5.7 μmol h–1 cm–2 at −0.4 V vs RHE. This combination of high FE and low onset potential is rarely achieved in NO3RR. The catalyst maintained stable performance over 12 consecutive 1 h chronoamperometric tests. Scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) analyses before and after electrolysis revealed a significant increase in nanowire diameter (from 97 to 562 nm), no changes in the crystalline structure, and partial reduction of Co3+ to Co2+ at the electrocatalyst surface, while preserving the Co3O4 phase. In situ X-ray absorption near edge structure (XANES) further confirmed the stability of the Co3O4/TiO2/Ti under operating conditions. These results provide a basis for future investigations aiming to enhance ammonia yield rate at even lower overpotentials.
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