Abstract
The production of monophenols from lignocellulose with cellulose intact without exogenous hydrogen via self-hydrogen supplied fractionation is promising, yet requires high metal loadings and yields saturated products. Herein, we report a single-atom alloyed Pt1Ni catalyst that achieves 50.9 wt% yield of phenolic monomers from birch sawdust with about 50% selectivity to valuable propenyl side-chained products under mild conditions (140 °C, 1 atm N2), while preserving cellulose intact. Reaction pathway studies and density functional theory calculations based on a β-O-4 model compound reveal three coexisting pathways. The Pt1Ni alloy preferentially promotes the dehydroxylation of Cα-OH and forms a key Cα = Cβ intermediate due to the oxygen affinity of Ni sites, and ultimately, enhance the production of valuable propenyl products via the synergistic effect of Pt and Ni. This work provides a strategy for maximizing Pt utilization and producing unsaturated chemicals from biomass under hydrogen-free conditions, advancing sustainable biorefining.
Similar content being viewed by others
Data availability
All data generated in this study are provided in the Supplementary Information/Source Data file. Source data are provided with this paper. All data are available from the corresponding author upon request. Source data are provided with this paper.
References
Tuck, C. O., Perez, E., Horvath, I. T., Sheldon, R. A. & Poliakoff, M. Valorization of biomass: deriving more value from waste. Science 337, 695–699 (2012).
Alonso, D. M. et al. Increasing the revenue from lignocellulosic biomass: maximizing feedstock utilization. Sci. Adv. 3, e1603301 (2017).
Corma, A., Iborra, S. & Velty, A. Chemical routes for the transformation of biomass into chemicals. Chem. Rev. 107, 2411–2502 (2007).
Huber, G. W., Iborra, S. & Corma, A. Synthesis of transportation fuels from biomass: chemistry, catalysts, and engineering. Chem. Rev. 106, 4044–4098 (2006).
Schutyser, W. et al. Chemicals from lignin: an interplay of lignocellulose fractionation, depolymerisation, and upgrading. Chem. Soc. Rev. 47, 852–908 (2018).
Sun, Z., Fridrich, B., De Santi, A., Elangovan, S. & Barta, K. Bright side of lignin depolymerization: toward new platform chemicals. Chem. Rev. 118, 614–678 (2018).
Zakzeski, J., Bruijnincx, P. C., Jongerius, A. L. & Weckhuysen, B. M. The catalytic valorization of lignin for the production of renewable chemicals. Chem. Rev. 110, 3552–3599 (2010).
Li, C., Zhao, X., Wang, A., Huber, G. W. & Zhang, T. Catalytic transformation of lignin for the production of chemicals and fuels. Chem. Rev. 115, 11559–11624 (2015).
Adler, A. et al. Lignin-first biorefining of Nordic poplar to produce cellulose fibers could displace cotton production on agricultural lands. Joule 6, 1845–1858 (2022).
Rinaldi, R. et al. Paving the way for lignin valorisation: recent advances in bioengineering, biorefining and catalysis. Angew. Chem. Int. Ed. 55, 8164–8215 (2016).
Van den Bosch, S. et al. Reductive lignocellulose fractionation into soluble lignin-derived phenolic monomers and dimers and processable carbohydrate pulps. Energy Environ. Sci. 8, 1748–1763 (2015).
Li, N. et al. Selective lignin arylation for biomass fractionation and benign bisphenols. Nature 630, 381–386 (2024).
Luo, H. et al. Oxidative catalytic fractionation of lignocellulosic biomass under non-alkaline conditions. J. Am. Chem. Soc. 143, 15462–15470 (2021).
Zhu, Y. et al. Oxidative catalytic fractionation of lignocellulose to high-yield aromatic aldehyde monomers and pure cellulose. ACS Catal. 13, 7929–7941 (2023).
Shuai, L. et al. Formaldehyde stabilization facilitates lignin monomer production during biomass depolymerization. Science 354, 329–333 (2016).
Abu-Omar, M. M. et al. Guidelines for performing lignin-first biorefining. Energy Environ. Sci. 14, 262–292 (2021).
Renders, T., Van den Bosch, S., Koelewijn, S.-F., Schutyser, W. & Sels, B. Lignin-first biomass fractionation: the advent of active stabilisation strategies. Energy Environ. Sci. 10, 1551–1557 (2017).
Zhai, Y. et al. Depolymerization of lignin via a non-precious Ni–Fe alloy catalyst supported on activated carbon. Green Chem. 19, 1895–1903 (2017).
Park, J. et al. Highly efficient reductive catalytic fractionation of lignocellulosic biomass over extremely low-loaded Pd catalysts. ACS Catal. 10, 12487–12506 (2020).
Liu, Z. et al. Rational highly dispersed ruthenium for reductive catalytic fractionation of lignocellulose. Nat. Commun. 13, 4716 (2022).
Ge, J. et al. Highly efficient metal-acid synergetic catalytic fractionation of lignocellulose under mild conditions over lignin-coordinated N-anchoring Co single-atom catalyst. Chem. Eng. J. 462, 142109 (2023).
Brienza, F. et al. Toward a hydrogen-free reductive catalytic fractionation of wheat straw biomass. ChemSusChem 16, e202300103 (2023).
Chen, J. et al. Efficient fractionation and catalytic valorization of raw biomass in ϵ-caprolactone and water. ChemSusChem 16, e202202162 (2023).
Zhang, K. et al. Catalytic hydrogenolysis of lignin into propenyl-monophenol over Ru single atoms supported on CeO2 with rich oxygen vacancies. ACS Catal. 14, 16115–16126 (2024).
Trullemans, L. et al. Renewable and safer bisphenol A substitutes enabled by selective zeolite alkylation. Nat. Sustain. 6, 1693–1704 (2023).
Galkin, M. V. & Samec, J. S. Selective route to 2-propenyl aryls directly from wood by a tandem organosolv and palladium-catalysed transfer hydrogenolysis. ChemSusChem 7, 2154–2158 (2014).
Li, Y. et al. Hydrogen-transfer reductive catalytic fractionation of lignocellulose: high monomeric yield with switchable selectivity. Angew. Chem. Int. Ed. 62, e202307116 (2023).
Wang, S., Zhang, K., Li, H., Xiao, L. P. & Song, G. Selective hydrogenolysis of catechyl lignin into propenylcatechol over an atomically dispersed ruthenium catalyst. Nat. Commun. 12, 416 (2021).
Wang, S., Li, X., Fu, C., Li, H. & Song, G. Atomically dispersed palladium driving reductive catalytic fractionation of lignocellulose into alkene-functionalized phenols. ACS Catal .14, 3565–3574 (2024).
Zhou, H., Liu, X., Guo, Y. & Wang, Y. Self-hydrogen supplied catalytic fractionation of raw biomass into lignin-derived phenolic monomers and cellulose-rich pulps. JACS Au 3, 1911–1917 (2023).
Wang, Y., Zhou, H., Guo, Y. & Liu, X. Method for preparing cellulose and lignin oil by depolymerizing lignocellulose without exogenous hydrogen. US Patent, Pub. No.: US WO/2024/124661 A1 (2024).
Hannagan, R. T., Giannakakis, G., Flytzani-Stephanopoulos, M. & Sykes, E. C. H. Single-atom alloy catalysis. Chem. Rev. 120, 12044–12088 (2020).
Zhang, T., Walsh, A. G., Yu, J. & Zhang, P. Single-atom alloy catalysts: structural analysis, electronic properties and catalytic activities. Chem. Soc. Rev. 50, 569–588 (2021).
Nakaya, Y. & Furukawa, S. Catalysis of alloys: classification, principles, and design for a variety of materials and reactions. Chem. Rev. 123, 5859–5947 (2023).
Song, W., Du, Q., Li, X., Wang, S. & Song, G. Sustainable production of bioactive molecules from c-lignin-derived propenylcatechol. ChemSusChem 15, e202200646 (2022).
Huang, H., Zhang, X., Ma, L. & Liao, Y. Reductive catalytic fractionation of lignocellulose toward propyl- or propenyl-substituted monomers and mechanistic understanding. Angew. Chem. Int. Ed. 64, e202502545 (2025).
Liu, Y., Zhang, L., Feng, S. & Chen, X. Promoting effect of Ni on the catalytic production of alanine from lactic acid over RuNi/AC catalyst. Ind. Eng. Chem. Res. 61, 10285–10293 (2022).
Li, D. et al. NiAl2O4 spinel supported Pt catalyst: high performance and origin in aqueous-phase reforming of methanol. ACS Catal. 9, 9671–9682 (2019).
Yan, B. et al. Dry reforming of ethane and butane with CO2 over PtNi/CeO2 bimetallic catalysts. ACS Catal. 6, 7283–7292 (2016).
Liu, W. et al. Highly-efficient RuNi single-atom alloy catalysts toward chemoselective hydrogenation of nitroarenes. Nat. Commun. 13, 3188 (2022).
Kikkawa, S., Teramura, K., Asakura, H., Hosokawa, S. & Tanaka, T. Isolated platinum atoms in Ni/γ-Al2O3 for selective hydrogenation of CO2 toward CH4. J. Phys. Chem. C 123, 23446–23454 (2019).
Li, Z. et al. Atomically dispersed Pt on the surface of Ni particles: synthesis and catalytic function in hydrogen generation from aqueous ammonia–borane. ACS Catal. 7, 6762–6769 (2017).
Zhou, H., Song, K., Guo, Y., Liu, X. & Wang, Y. Selective production of 4-Propylphenol from lignin oil without exogenous hydrogen over a RuNi/NiAl2O4 catalyst. ACS Sustain. Chem. Eng. 11, 15052–15059 (2023).
Kayode, G. O. & Montemore, M. M. Factors controlling oxophilicity and carbophilicity of transition metals and main group metals. J. Mater. Chem. A 9, 22325–22333 (2021).
Li, L. et al. Hydrogen-free production of 4-Alkylphenols from Lignin via self-reforming-driven depolymerization and hydrogenolysis. ACS Catal. 10, 15197–15206 (2020).
Ravel, B. & Newville, M. ATHENA,ARTEMIS,HEPHAESTUS: data analysis for X-ray absorption spectroscopy using IFEFFIT. J. Synchrotron. Radiat. 12, 537–541 (2005).
Scanlon, J. T. & Willis, D. E. Calculation of flame ionization detector relative response factors using the effective carbon number concept. J. Chromatogr. Sci. 23, 333–340 (1985).
Kresse, G. & Furthmüller, J. Efficiency of ab-initio total energy calculations for metals and semiconductors using a plane-wave basis set. Comp. Mater. Sci. 6, 15–50 (1996).
Kresse, G. & Hafner, J. Ab initio molecular dynamics for liquid metals. Phys. Rev. B Condens Matter. 47, 558–561 (1993).
Kresse, G. & Hafner, J. Ab initio molecular-dynamics simulation of the liquid-metal-amorphous-semiconductor transition in germanium. Phys. Rev. B Condens Matter. 49, 14251–14269 (1994).
Kresse, G. & Furthmüller, J. Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set. Phys. Rev. B 54, 11169 (1996).
Grimme, S., Antony, J., Ehrlich, S. & Krieg, H. A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. J. Chem. Phys. 132, 154104 (2010).
Grimme, S., Ehrlich, S. & Goerigk, L. Effect of the damping function in dispersion corrected density functional theory. J. Comput .Chem. 32, 1456–1465 (2011).
Cao, X.-M., Burch, R., Hardacre, C. & Hu, P. An understanding of chemoselective hydrogenation on crotonaldehyde over Pt(111) in the free energy landscape: the microkinetics study based on first-principles calculations. Catal. Today 165, 71–79 (2011).
Sun, X., Cao, X. & Hu, P. Theoretical insight into the selectivities of copper-catalyzing heterogeneous reduction of carbon dioxide. Sci China-Chem 58, 553–564 (2015).
Zhang, L., Shao, Z.-J., Cao, X.-M. & Hu, P. Insights into different products of nitrosobenzene and nitrobenzene hydrogenation on Pd (111) under realistic reaction conditions. J. Phys. Chem. C 122, 20337–20350 (2018).
Hu, W., Lan, J., Guo, Y., Cao, X.-M. & Hu, P. Origin of efficient catalytic combustion of methane over Co3O4(110): active low-coordination lattice oxygen and cooperation of multiple active sites. ACS Catal. 6, 5508–5519 (2016).
Alavi, A., Hu, P., Deutsch, T., Silvestrelli, P. L. & Hutter, J. CO oxidation on Pt (111): an ab initio density functional theory study. Phys. Rev. Lett. 80, 3650 (1998).
Nelson, R. et al. LOBSTER: local orbital projections, atomic charges, and chemical-bonding analysis from projector-augmented-wave-based density-functional theory. J. Comput. Chem. 41, 1931–1940 (2020).
Deringer, V. L., Tchougreeff, A. L. & Dronskowski, R. Crystal orbital Hamilton population (COHP) analysis as projected from plane-wave basis sets. J. Phys. Chem. A 115, 5461–5466 (2011).
Zhang, L., Cao, X.-M. & Hu, P. Insight into chemoselectivity of nitroarene hydrogenation: a DFT-D3 study of nitroarene adsorption on metal surfaces under the realistic reaction conditions. Appl. Surf. Sci. 392, 456–471 (2017).
Acknowledgements
The authors thank the financially supports by the National Key Research and Development Program of China (2022YFA1504903, 2022YFA1504904, 2023YFA1507601) (Y.Q.W.) and assistance with XAS measurement from Canadian Light Source.
Author information
Authors and Affiliations
Contributions
H.Z., Z.R.G., K.P.S., X.H.L., and Y.G.: preparation and characterization of catalysts, and performing the catalytic reactions. Q.X. and X.M.C.: DFT calculations. M.S. and Y.F.H.: collection and analysis of XAS data. X.M.C. and Y.Q.W.: overall direction of the project. H.Z., Q.X., X.M.C., and Y.Q.W. wrote the manuscript with the help from all authors.
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Nature Communications thanks Yu Jing, Mingyang Liu, and Zhicheng Luo for their contribution to the peer review of this work. A peer review file is available.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Source data
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
Cite this article
Zhou, H., Xiang, Q., Guo, Z. et al. Efficient Pt1Ni single-atom alloy catalyst for hydrogen-free catalytic fractionation of lignocellulose. Nat Commun (2026). https://doi.org/10.1038/s41467-026-70993-0
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467-026-70993-0


