Pt和Pd在TiO2纳米管上的电化学沉积及其在生物甲烷和沼气光电催化转化制氢中的应用

IF 2.7 4区 化学 Q3 CHEMISTRY, PHYSICAL
Laís Bresciani, Simone Stülp
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引用次数: 0

摘要

利用半导体材料对生物甲烷/沼气进行光电催化转化是一种很有前途的生产未来燃料——绿色H2的方法。本文采用循环伏安法对电化学阳极氧化法制备的TiO2纳米管(TiO2NTs)进行了Pt和Pd纳米粒子的电化学沉积修饰,分别制备了TiO2NTs/Pt和TiO2NTs/Pd催化剂。利用扫描电子显微镜、能量色散光谱和x射线衍射对材料的形态、组成和结晶度进行评价。采用线性扫描伏安法、计时安培法和电化学阻抗法研究了电极的光活性。在TiO2NTs上引入Pt和Pd,使得电极具有优异的光电电荷分离和转移性能。在甲烷的存在下,得到的电流密度进一步增加,与纯tio2相比,TiO2NTs/Pt和TiO2NTs/Pd电极分别增加了约2.23倍和2.95倍,证实了CH4的空穴清除剂作用。甲烷光电催化转化氢气的最大产氢量分别为120.7、304.7和393 mmol。对于TiO2NTs, TiO2NTs/Pt和TiO2NTs/Pd电极分别为cm−2,清楚地显示了电沉积在TiO2NTs表面的金属纳米颗粒的积极贡献。在沼气的光电催化转化过程中,氢气的产生量较低,并可能发生额外的反应,如CO2的还原。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrochemical Deposition of Pt and Pd on TiO2 Nanotubes for Application in the Photoelectrocatalytic Conversion of Biomethane and Biogas for Hydrogen Generation

Electrochemical Deposition of Pt and Pd on TiO2 Nanotubes for Application in the Photoelectrocatalytic Conversion of Biomethane and Biogas for Hydrogen Generation

Electrochemical Deposition of Pt and Pd on TiO2 Nanotubes for Application in the Photoelectrocatalytic Conversion of Biomethane and Biogas for Hydrogen Generation

The photoelectrocatalytic conversion of biomethane/biogas using semiconductor materials is a promising method for production of green H2, the fuel of the future. In this work, TiO2 nanotubes (TiO2NTs) prepared by electrochemical anodization were modified with Pt and Pd nanoparticles by electrochemical deposition using cyclic voltammetry, producing TiO2NTs/Pt and TiO2NTs/Pd catalysts, respectively. Evaluation of the morphology, composition, and crystallinity of the materials employed scanning electron microscopy, energy dispersive spectroscopy, and X-ray diffraction. The photoactivities of the electrodes were studied using linear scanning voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. The introduction of Pt and Pd on the TiO2NTs resulted in electrodes that presented excellent photogenerated charge separation and transfer properties. In the presence of methane, the current densities obtained increased further, by around 2.23- and 2.95-fold for the TiO2NTs/Pt and TiO2NTs/Pd electrodes, respectively, compared to the pure TiO2NTs, confirming the capacity of CH4 to act as a hole scavenger. The maximum amounts of H2 obtained from the photoelectrocatalytic conversion of methane were 120.7, 304.7, and 393 mmol.cm−2 for the TiO2NTs, TiO2NTs/Pt, and TiO2NTs/Pd electrodes, respectively, clearly showing the positive contribution of the metallic nanoparticles electrodeposited on the TiO2NTs surface. A lower amount of H2 was produced in the photoelectrocatalytic conversion of biogas, with the possible occurrence of additional reactions, such as the reduction of CO2.

Graphical Abstract

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来源期刊
Electrocatalysis
Electrocatalysis CHEMISTRY, PHYSICAL-ELECTROCHEMISTRY
CiteScore
4.80
自引率
6.50%
发文量
93
审稿时长
>12 weeks
期刊介绍: Electrocatalysis is cross-disciplinary in nature, and attracts the interest of chemists, physicists, biochemists, surface and materials scientists, and engineers. Electrocatalysis provides the unique international forum solely dedicated to the exchange of novel ideas in electrocatalysis for academic, government, and industrial researchers. Quick publication of new results, concepts, and inventions made involving Electrocatalysis stimulates scientific discoveries and breakthroughs, promotes the scientific and engineering concepts that are critical to the development of novel electrochemical technologies. Electrocatalysis publishes original submissions in the form of letters, research papers, review articles, book reviews, and educational papers. Letters are preliminary reports that communicate new and important findings. Regular research papers are complete reports of new results, and their analysis and discussion. Review articles critically and constructively examine development in areas of electrocatalysis that are of broad interest and importance. Educational papers discuss important concepts whose understanding is vital to advances in theoretical and experimental aspects of electrochemical reactions.
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