Sulfur-engineered rhenium single-atoms on borides for tunable syngas and lactic acid co-production

The simultaneous and selective production of syngas and value-added chemicals from biomass-derived feedstocks is fundamentally restricted by sluggish multi-electron-proton transfer and the lack of precisely defined active sites capable of stabilizing reactive intermediates. Here, we report a sulfur-mediated coordination reconstruction strategy that transforms metastable rhenium species on two-dimensional chromium boride into uniformly dispersed Re–S4 single atoms. The electronic environment of Re–S4 optimizes the d-band center, stabilizing the key intermediate glyceraldehyde for selective C-C bond cleavage. In this work, the synergistic combination of atomic-scale engineering and reactant kinetics modulation yields a total syngas rate of 34.08 mmol g−1 h−1 with a wide-ranging tunable H2/CO ratio (0.1 to 14.4), alongside a lactic acid yield of 90.8%. The system’s robustness is further validated via large-scale outdoor sunlight-tracking tests, demonstrating its potential as a scalable, sustainable biorefinery technology for the concurrent production of gas-phase fuels and liquid-phase platform chemicals. By engineering Re–S4 single atoms via sulfur-mediated coordination reconstruction strategy, researchers achieved a total syngas rate of 34.08 mmol g−1 h−1 with a wide-ranging tunable H2/CO ratio (0.1 to 14.4), alongside a lactic acid yield of 90.8%.

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Publication Details

Journal
Nature Communications
Published
2026-06-09
DOI
https://doi.org/10.1038/s41467-026-73876-6
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.00

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article

Sulfur-engineered rhenium single-atoms on borides for tunable syngas and lactic acid co-production

Tsz Woon Benedict Lo, Qiong Liu, Jimei Li, Yushun Han et al.
Nature Communications
Catalysts for Methane Reforming
article

Sulfur-engineered rhenium single-atoms on borides for tunable syngas and lactic acid co-production

Tsz Woon Benedict Lo, Qiong Liu, Jimei Li, Yushun Han, Weikang Ling, Runcang Sun, Wei Quan, Jiliang Ma
article en

Abstract

The simultaneous and selective production of syngas and value-added chemicals from biomass-derived feedstocks is fundamentally restricted by sluggish multi-electron-proton transfer and the lack of precisely defined active sites capable of stabilizing reactive intermediates. Here, we report a sulfur-mediated coordination reconstruction strategy that transforms metastable rhenium species on two-dimensional chromium boride into uniformly dispersed Re–S4 single atoms. The electronic environment of Re–S4 optimizes the d-band center, stabilizing the key intermediate glyceraldehyde for selective C-C bond cleavage. In this work, the synergistic combination of atomic-scale engineering and reactant kinetics modulation yields a total syngas rate of 34.08 mmol g−1 h−1 with a wide-ranging tunable H2/CO ratio (0.1 to 14.4), alongside a lactic acid yield of 90.8%. The system’s robustness is further validated via large-scale outdoor sunlight-tracking tests, demonstrating its potential as a scalable, sustainable biorefinery technology for the concurrent production of gas-phase fuels and liquid-phase platform chemicals. By engineering Re–S4 single atoms via sulfur-mediated coordination reconstruction strategy, researchers achieved a total syngas rate of 34.08 mmol g−1 h−1 with a wide-ranging tunable H2/CO ratio (0.1 to 14.4), alongside a lactic acid yield of 90.8%.

Nature Communications
Hong Kong Polytechnic University (HK), Jinan University (CN), Dalian Polytechnic University (CN)
National Natural Science Foundation of China, China Agricultural University, Hong Kong Polytechnic University, Natural Science Foundation of Liaoning Province, Environment and Conservation Fund, South China Agricultural University, Guangdong Academy of Sciences
Industry, innovation and infrastructure
Openalex Percentile: Top 18%
Catalysts for Methane Reforming
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