光化学合成高效Pt/TiO2催化剂,用于CO2热还原为CO

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL
Zhanglong Guo , Li Wang , Jiacheng Zhang , Hongmei Zhou , Jianli Yang , Xin Xiao
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引用次数: 0

摘要

负载型铂(Pt)催化剂对于CO2热还原至关重要,但传统的制备方法往往产生较低的催化活性。本研究通过开发一种光化学沉积方法,仅以水为溶剂合成高效Pt/TiO2催化剂(Pt/TiO2- l),解决了这一挑战。与传统制备的催化剂相比,Pt/TiO2-L催化剂在600℃下的CO2转化率高达65%,且操作稳定。透射电镜结果显示,纳米Pt颗粒在TiO2载体上均匀分散(约1 nm)。XPS分析表明,Pt/TiO2-L的表面Pt含量较高,具有更多的CO2还原活性位点。原位CO- drifts证实,由于表面Pt含量较高,Pt/TiO2-L对CO的吸附增强。本研究表明,光化学途径是合成高效Pt/TiO2热还原CO2催化剂的一种简单有效的方法,在绿色化学领域具有广阔的工业应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Photochemical synthesis of highly efficient Pt/TiO2 catalyst for thermal CO2 reduction to CO

Photochemical synthesis of highly efficient Pt/TiO2 catalyst for thermal CO2 reduction to CO
Supported platinum (Pt) catalysts are crucial for thermal CO2 reduction, yet traditional preparation methods often yield low catalytic activity. This study addresses this challenge by developing a photochemical deposition method to synthesize highly efficient Pt/TiO2 catalysts (Pt/TiO2-L) using only water as the solvent. The Pt/TiO2-L catalyst exhibited significantly higher CO2 conversion rates as 65 % at 600 °C and operational stability compared to traditionally prepared catalysts. TEM result revealed uniform dispersion of small Pt nanoparticles (around 1 nm) on the TiO2 support. XPS analysis showed a higher Pt surface content in Pt/TiO2-L, resulting in more active sites for CO2 reduction. In-situ CO-DRIFTS confirmed enhanced CO adsorption on Pt/TiO2-L due to its higher surface Pt content. This work demonstrates that the photochemical route is an effective and simple method for synthesizing efficient Pt/TiO2 catalysts for thermal CO2 reduction, offering promising prospects for industrial application in green chemistry.
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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