Measuring and directing charge transfer in heterogenous catalysts

Michael J. Zachman, Victor Fung, Felipe Polo-Garzon, Shaohong Cao, Jisue Moon, Zhennan Huang, De en Jiang, Zili Wu, Miaofang Chi

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

Precise control of charge transfer between catalyst nanoparticles and supports presents a unique opportunity to enhance the stability, activity, and selectivity of heterogeneous catalysts. While charge transfer is tunable using the atomic structure and chemistry of the catalyst-support interface, direct experimental evidence is missing for three-dimensional catalyst nanoparticles, primarily due to the lack of a high-resolution method that can probe and correlate both the charge distribution and atomic structure of catalyst/support interfaces in these structures. We demonstrate a robust scanning transmission electron microscopy (STEM) method that simultaneously visualizes the atomic-scale structure and sub-nanometer-scale charge distribution in heterogeneous catalysts using a model Au-catalyst/SrTiO3-support system. Using this method, we further reveal the atomic-scale mechanisms responsible for the highly active perimeter sites and demonstrate that the charge transfer behavior can be readily controlled using post-synthesis treatments. This methodology provides a blueprint for better understanding the role of charge transfer in catalyst stability and performance and facilitates the future development of highly active advanced catalysts.

Original languageEnglish
Article number3253
JournalNature Communications
Volume13
Issue number1
DOIs
StatePublished - Dec 2022

Funding

Research was sponsored by the US DOE, Office of Science, Office of Basic Energy Sciences (BES), Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science program. Technique development and data analysis were supported by US DOE Office of Science under Early Career award no. ERKCZ55. All microscopy research was supported by the Center for Nanophase Materials Sciences (CNMS), which is a US Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. We would like to thank Nina Balke for useful conversations. This research used resources of the National Energy Research Scientific Computing Center, a DOE Office of Science User Facility supported under contract no. DE-AC02-05CH11231.

FundersFunder number
Center for Nanophase Materials Sciences
U.S. Department of Energy
Office of ScienceDE-AC02-05CH11231, ERKCZ55
Basic Energy Sciences
Oak Ridge National Laboratory

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