Tuning the Local Coordination and Electronic Metal–Support Interaction of Pd Single-Atom Catalysts for Methane Combustion

Abstract Tuning the local coordination environment and electronic metal–support interaction (EMSI) via support modulation is critical for optimizing the catalytic performance of Pd single-atom catalysts (SACs) in methane (CH4) combustion. Yet their synergistic regulation remains elusive. Herein, a series of Pd1/M SACs (M = NiO, SnO2, TiO2, and CeO2) with identical Pd loadings was facilely prepared using a one-step flame spray pyrolysis (FSP) method. The results reveal that support modulation tunes the local coordination environment and EMSI in Pd1/M SACs, thereby influencing their catalytic performance and stability in CH4 combustion. A coupled coordination–defect–electronic effect arises from strong EMSI and abundant oxygen vacancies (OV) in Pd1/NiO. This effect facilitates CH4 adsorption and activation, resulting in the lowest T50 (357 °C) and enhanced stability compared with Pd1/TiO2, which exhibits moderate EMSI. In contrast, CeO2 stabilizes an over-coordinated Pd–O4.3 local environment under weak EMSI, leading to a CH4 conversion of less than 10% at 450 °C. In-situ diffuse reflectance infrared Fourier transform spectroscopy, in-situ X-ray absorption spectroscopy combined with density functional theory (DFT) calculations reveal that CH4 combustion over Pd1/NiO follows the Mars–van Krevelen mechanism: Pd1–OV–Ni active sites serve as adsorption and activation centers for gaseous CH4, and lattice oxygen subsequently converts the adsorbed reactant into CO2 via formate and carbonate intermediates. By contrast, the over-coordinated Pd single atoms in Pd1/CeO2 exhibit poor CH4 adsorption and activation, resulting in the surface accumulation of abundant formate and carbonate intermediates that cannot be further converted into CO2. This work provides crucial insights into tuning the local coordination environment and EMSI via support modulation for simultaneously achieving high activity and stability in Pd SACs.

Authors

Institutions

Publication Details

Journal
ACS Catalysis
Published
2026-09-18
DOI
https://doi.org/10.1021/acscatal.6c04799
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Tuning the Local Coordination and Electronic Metal–Support Interaction of Pd Single-Atom Catalysts for Methane Combustion

Ruihan Wang, Xin Huang, Jiangliang Hu, Qian Liu et al.
ACS Catalysis
Catalytic Processes in Materials Science
article

Tuning the Local Coordination and Electronic Metal–Support Interaction of Pd Single-Atom Catalysts for Methane Combustion

Ruihan Wang, Xin Huang, Jiangliang Hu, Qian Liu, Jiancheng Wang, Jianxin Liu, Bing Wang, Yahui Wang
article en

Abstract

Abstract Tuning the local coordination environment and electronic metal–support interaction (EMSI) via support modulation is critical for optimizing the catalytic performance of Pd single-atom catalysts (SACs) in methane (CH4) combustion. Yet their synergistic regulation remains elusive. Herein, a series of Pd1/M SACs (M = NiO, SnO2, TiO2, and CeO2) with identical Pd loadings was facilely prepared using a one-step flame spray pyrolysis (FSP) method. The results reveal that support modulation tunes the local coordination environment and EMSI in Pd1/M SACs, thereby influencing their catalytic performance and stability in CH4 combustion. A coupled coordination–defect–electronic effect arises from strong EMSI and abundant oxygen vacancies (OV) in Pd1/NiO. This effect facilitates CH4 adsorption and activation, resulting in the lowest T50 (357 °C) and enhanced stability compared with Pd1/TiO2, which exhibits moderate EMSI. In contrast, CeO2 stabilizes an over-coordinated Pd–O4.3 local environment under weak EMSI, leading to a CH4 conversion of less than 10% at 450 °C. In-situ diffuse reflectance infrared Fourier transform spectroscopy, in-situ X-ray absorption spectroscopy combined with density functional theory (DFT) calculations reveal that CH4 combustion over Pd1/NiO follows the Mars–van Krevelen mechanism: Pd1–OV–Ni active sites serve as adsorption and activation centers for gaseous CH4, and lattice oxygen subsequently converts the adsorbed reactant into CO2 via formate and carbonate intermediates. By contrast, the over-coordinated Pd single atoms in Pd1/CeO2 exhibit poor CH4 adsorption and activation, resulting in the surface accumulation of abundant formate and carbonate intermediates that cannot be further converted into CO2. This work provides crucial insights into tuning the local coordination environment and EMSI via support modulation for simultaneously achieving high activity and stability in Pd SACs.

ACS Catalysis
Shanxi University (CN), Taiyuan University of Science and Technology (CN), Taiyuan University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 24%
Catalytic Processes in Materials Science
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.