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

Abstract

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.

Abstract Image

光化学合成高效Pt/TiO2催化剂,用于CO2热还原为CO
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。
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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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