Understanding stability and reactivity of transition metal single-atoms on graphene
Recently, single-atom catalysts (SACs) based on transition metals (TMs) have been identified as highly active catalysts with excellent atomic efficiency, reduced consumption of expensive materials, well-defined active centers, and tunable activity and selectivity. Furthermore, when carbon-based supports (including graphene-derived materials) are employed in SACs, their unique structural and electronic properties, such as high electrical conductivity and mechanical strength, can be integrated. However, for this application, the primary objective is to maintain proper stability-reactivity balance, ensuring the system remains stable while preserving its high chemical activity. In this context, we explore the adsorption behavior of TM single atoms (Co, Ni, Rh, Pd, Ir, Pt) on pristine graphene (pGR), hexagonal boron nitride (hBN), and graphene with monovacancies (GRm) using DFT-PBE+D3 calculations. From the adsorption energy trends, we observe weak chemisorption on pGR and physisorption on hBN, with adsorption energies ranging from 0.5 eV (Co/hBN) to 1.80 eV (Rh/pGR). In contrast, the adsorption strength is significantly enhanced on GRm (strong chemisorption), with adsorption energies reaching up to 9.11 eV for Ir/GRm, attributed to the strong defect-induced reactivity and improved orbital overlap. Electronic structure analysis reveals that pGR retains its semimetallic nature, hBN remains an insulator, and GRm transitions to metallic behavior due to the strong interactions between TM-C. Bader charge analysis indicates significant charge transfer in GRm, consistent with its catalytic potential, while hybridization indices show substantial pd orbital mixing, favoring improved TM anchoring. Thus, our results identify GRm as the most promising substrate for SACs, pGR as a balanced platform for controlled reactivity, and hBN as a stable support for selective catalysis or dielectric applications. Finally, defect engineering is a powerful strategy for designing next-generation catalysts, ensuring the right balance between stability and reactivity.
Authors
- Maurício J. Piotrowski (ORCID: https://orcid.org/0000-0003-3477-4437)
- Celso R. C. Rêgo (ORCID: https://orcid.org/0000-0003-1861-2438)
- Gabriel Reynald Da Silva
- Diego Guedes‐Sobrinho (ORCID: https://orcid.org/0000-0002-3313-2822)
- Wesley Oliveira Morais
- Vítor Sousa (ORCID: https://orcid.org/0000-0003-3219-1078)
- Alexandre C. Dias (ORCID: https://orcid.org/0000-0001-5934-8528)
- João Paulo Cerqueira Felix (ORCID: https://orcid.org/0000-0002-7064-9660)
- Carlos M. O. Bastos (ORCID: https://orcid.org/0000-0002-9988-5202)
- Efrácio Mamani Flores (ORCID: https://orcid.org/0000-0001-7018-3779)
Institutions
- Universidade de Brasília (BR)
- Universidade Federal de Pelotas (BR)
- Jorge Basadre Grohmann National University (PE)
- Universidade do Estado do Rio de Janeiro (BR)
- Universidade Federal do Paraná (BR)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-05-03
- DOI
- https://doi.org/10.1038/s41598-025-00126-y
- Citations
- 6
- Primary Topic
- Graphene research and applications
- Type
- article
- Field-Weighted Citation Impact
- 3.11
Funders
- Karlsruhe Institute of Technology
- Universidade Federal de Pelotas
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
- Bundesministerium für Bildung und Forschung
- Ministério da Ciência, Tecnologia e Inovação
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul
- Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
- Financiadora de Estudos e Projetos
- Universidade Federal do Rio Grande do Sul
- Fundação de Apoio à Pesquisa do Distrito Federal
- Universidade Estadual de Campinas
- Universidade Federal do Paraná
- Universidade Federal do Rio de Janeiro
- Centro Nacional de Processamento de Alto Desempenho em São Paulo