Enzyme-inspired single-atom photocatalysis for oxygen reduction to hydrogen peroxide

Photocatalysis presents a promising route for generating sustainable, high-energy-density fuels. However, conventional photocatalysts based on rigid binary metal compounds face significant limitations, including fixed band gaps, rapid charge recombination, and non-specific reaction pathways - ultimately leading to limited selectivity and yield. Critically, they lack the site-specific selectivity characteristic of enzymatic systems, a feature essential for achieving high efficiency, control, and precision. Inspired by cytochrome c oxidase, we report the development of Cu-single-atom-enhanced carbon dots as the enzymatic-like photocatalyst. By mimicking enzyme´s site-specific electron transfer cascade, these carbon dots enable the selective photocatalytic reduction of oxygen to hydrogen peroxide under ambient conditions. This study introduces a strategy for translating enzymatic precision into photocatalytic materials design, bridging molecular and materials catalysis for sustainable energy and chemical transformations.

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Publication Details

Journal
Nature Communications
Published
2025-12-07
DOI
https://doi.org/10.1038/s41467-025-67189-3
Citations
2
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
1.04

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article

Enzyme-inspired single-atom photocatalysis for oxygen reduction to hydrogen peroxide

David Panáček, Dirk M. Guldi, Giorgio Zoppellaro, Radek Zbořil et al.
2 citations
Nature Communications
Advanced Nanomaterials in Catalysis
1.04
article

Enzyme-inspired single-atom photocatalysis for oxygen reduction to hydrogen peroxide

David Panáček, Dirk M. Guldi, Giorgio Zoppellaro, Radek Zbořil, María Ana Huergo, Camila Otero, Emiliano Fonda, Zdeňěk Baďura, Štěpán Kment, Lukáš Zdražil, Hana Kmentová, Alejandro Cadranel, Ayse Günay‐Gürer
article en
2 citations

Abstract

Photocatalysis presents a promising route for generating sustainable, high-energy-density fuels. However, conventional photocatalysts based on rigid binary metal compounds face significant limitations, including fixed band gaps, rapid charge recombination, and non-specific reaction pathways - ultimately leading to limited selectivity and yield. Critically, they lack the site-specific selectivity characteristic of enzymatic systems, a feature essential for achieving high efficiency, control, and precision. Inspired by cytochrome c oxidase, we report the development of Cu-single-atom-enhanced carbon dots as the enzymatic-like photocatalyst. By mimicking enzyme´s site-specific electron transfer cascade, these carbon dots enable the selective photocatalytic reduction of oxygen to hydrogen peroxide under ambient conditions. This study introduces a strategy for translating enzymatic precision into photocatalytic materials design, bridging molecular and materials catalysis for sustainable energy and chemical transformations.

Nature CommunicationsVol. 16(1)
VSB - Technical University of Ostrava (CZ), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), International Council on Mining and Metals (GB), Synchrotron soleil (FR), Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (AR), Regional Centre of Advanced Technologies and Materials (CZ), Center for Advanced Aerospace Technologies (ES), Instituto de Química y Fisicoquímica Biológicas (AR), Fundación Ciencias Exactas y Naturales (AR), Palacký University Olomouc (CZ)
Solar Technologies go Hybrid, European Commission, Deutsche Forschungsgemeinschaft, Grantová Agentura České Republiky, Consejo Nacional de Investigaciones Científicas y Técnicas, HORIZON EUROPE Framework Programme, European Regional Development Fund, European Social Fund
Openalex Percentile: Top 21%
Advanced Nanomaterials in Catalysis
1.04
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