Interface Engineering of PdPt Ultrafine Ethanol Electro‐Oxidation Nanocatalysts by Bacterial Soluble Extracellular Polymeric Substances (s‐EPS) to Break through Sabatier Principle

Author:

Liu Chang1ORCID,Tang Qinyuan1,Fan Puyang1,Wei Yuhui1,Yu Yang1,Wen Xinwei1,Li Xianghong2,Li Lei3,Qu Qing1ORCID

Affiliation:

1. School of Chemical Science and Technology Yunnan University Kunming 650500 China

2. Key Laboratory of State Forestry and Grassland Administration on Highly‐Efficient Utilization of Forestry Biomass Resources in Southwest China & College of Materials and Chemical Engineering Southwest Forestry University Kunming 650224 China

3. State Key Laboratory for Conservation and Utilization of Bio‐resources in Yunnan Yunnan University Kunming 650500 China

Abstract

AbstractUnsatisfactory performance of ethanol oxidation reaction (EOR) catalysts hinders the application of direct ethanol fuel cells (DEFCs), while traditional alloy catalysts (like PdPt) is cursed by Sabatier principle due to countable active site types. However, bacterial soluble extracellular polymeric substances (s‐EPS) owning abundent functional groups may help breacking through it by contrusting different active sites on PdPt and inducing them to play synergy effect, which is called interface engineering. Using s‐EPS to engineer catalysts is more green and consumes lower energy compared to chemical reagents. Herein, PdPt alloy nanoparticles (≈2.1 nm) are successfully in situ synthesized by/on s‐EPS of Bacillus megaterium, an ex‐holotype. Tryptophan residuals are proved as the main reductant. In EOR, PdPt@s‐EPS shows higher activity (3.89 mA cm−2) than Pd@s‐EPS, Pt@s‐EPS, Pt/C and most reported akin catalysts. Its stability and durability are excellent, too. DFT modelling further demonstrates that, interface engineering by s‐EPS breaks through Sabatier principle, by the synergy of diverse sites owning different degrees of d‐p orbital hybridization. This work not only makes DEFCs closer to practice, but provides a facile and green strategy to design more catalysts.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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