Yichen Nie, Xingyong Li, Misbah Uddin, Na Liu, Senshen Yu, Phidsavard Keomeesay, Olajide-rasheed Olalekan, Shuaizhe Li, Yubao Chen, Xuebing Zhao, Longlong Ma, Zhifeng Zheng and Shijie Liu
{"title":"Rational design of an efficient Pt3Cu/TiO2 icosahedral catalyst for bio-aviation fuel production under mild conditions†","authors":"Yichen Nie, Xingyong Li, Misbah Uddin, Na Liu, Senshen Yu, Phidsavard Keomeesay, Olajide-rasheed Olalekan, Shuaizhe Li, Yubao Chen, Xuebing Zhao, Longlong Ma, Zhifeng Zheng and Shijie Liu","doi":"10.1039/D5GC01235J","DOIUrl":null,"url":null,"abstract":"<p >Bio-aviation fuel is a promising alternative sustainable aviation fuel (SAF) to fossil-based jet fuels. In this study, we employed a hydrothermal method to synthesize a novel Pt<small><sub>3</sub></small>Cu/TiO<small><sub>2</sub></small> icosahedral catalyst for the efficient hydrodeoxygenation (HDO) of oils and fats, enabling the highly selective production of alkanes. Characterization results confirmed the formation of Pt–Cu alloy nanoclusters in the Pt<small><sub>3</sub></small>Cu/TiO<small><sub>2</sub></small> icosahedra. The catalyst exhibited excellent catalytic performance, achieving 100% conversion of oil feedstock and 91.8% selectivity towards bio-aviation fuel under mild conditions (120 °C, 0.4 MPa H<small><sub>2</sub></small>). Additionally, the selectivity towards C<small><sub>8</sub></small>–C<small><sub>17</sub></small> alkanes was maintained at 50.1% after cycling the Pt<small><sub>3</sub></small>Cu/TiO<small><sub>2</sub></small> icosahedra for ten cycles. Density functional theory (DFT) calculations using propionic acid (PA) as a model molecule revealed that the hydrodecarbonylation reaction begins with the removal of OH* and H* from adsorbed PA on the Pt<small><sub>3</sub></small>Cu (111) planes, forming CH<small><sub>3</sub></small>CCO*, while the conversion of CH<small><sub>3</sub></small>CH<small><sub>2</sub></small>COOH to CH<small><sub>3</sub></small>CH<small><sub>2</sub></small>CO* and OH* was identified as the rate-limiting step.</p>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":" 22","pages":" 6449-6463"},"PeriodicalIF":9.3000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/gc/d5gc01235j","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Bio-aviation fuel is a promising alternative sustainable aviation fuel (SAF) to fossil-based jet fuels. In this study, we employed a hydrothermal method to synthesize a novel Pt3Cu/TiO2 icosahedral catalyst for the efficient hydrodeoxygenation (HDO) of oils and fats, enabling the highly selective production of alkanes. Characterization results confirmed the formation of Pt–Cu alloy nanoclusters in the Pt3Cu/TiO2 icosahedra. The catalyst exhibited excellent catalytic performance, achieving 100% conversion of oil feedstock and 91.8% selectivity towards bio-aviation fuel under mild conditions (120 °C, 0.4 MPa H2). Additionally, the selectivity towards C8–C17 alkanes was maintained at 50.1% after cycling the Pt3Cu/TiO2 icosahedra for ten cycles. Density functional theory (DFT) calculations using propionic acid (PA) as a model molecule revealed that the hydrodecarbonylation reaction begins with the removal of OH* and H* from adsorbed PA on the Pt3Cu (111) planes, forming CH3CCO*, while the conversion of CH3CH2COOH to CH3CH2CO* and OH* was identified as the rate-limiting step.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.