Photocatalytic production of ethylene and propionic acid from plastic waste by titania-supported atomically dispersed Pd species

Author:

Zhang Shuai1ORCID,Xia Bingquan2ORCID,Qu Yang3ORCID,Jing Liqiang3,Jaroniec Mietek4ORCID,Ran Jingrun1ORCID,Qiao Shi-Zhang1ORCID

Affiliation:

1. School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA 5005, Australia.

2. Key Laboratory for Green Chemical Process of Ministry of Education, School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan, Hubei 430074, China.

3. Key Laboratory of Functional Inorganic Material Chemistry (Ministry of Education), School of Chemistry and Materials Science, International Joint Research Center for Catalytic Technology, Heilongjiang University, Harbin, Heilongjiang 150080, China.

4. Department of Chemistry and Biochemistry & Advanced Materials and Liquid Crystal Institute, Kent State University, Kent, OH 44242, USA.

Abstract

Current chemical recycling of bulk synthetic plastic, polyethylene (PE), operates at high temperature/pressure and yields a complex mixture of products. PE conversion under mild conditions and with good selectivity toward value-added chemicals remains a practical challenge. Here, we demonstrate an atomic engineering strategy to modify a TiO 2 photocatalyst with reversible Pd species for the selective conversion of PE to ethylene (C 2 H 4 ) and propionic acid via dicarboxylic acid intermediates under moderate conditions. TiO 2 -supported atomically dispersed Pd species exhibits C 2 H 4 evolution of 531.2 μmol g cat −1 hour −1 , 408 times that of pristine TiO 2 . The liquid product is a valuable chemical propanoic acid with 98.8% selectivity. Plastic conversion with a C 2 hydrocarbon yield of 0.9% and a propionic acid yield of 6.3% was achieved in oxidation coupled with 3 hours of photoreaction. In situ spectroscopic studies confirm a dual role of atomic Pd species: an electron acceptor to boost charge separation/transfer for efficient photoredox, and a mediator to stabilize reaction intermediates for selective decarboxylation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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