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A molten-salt dispersion of lanthanides at the atomic scale

Haoyuan Wang
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⚡ Quantum Brief
Chinese researchers developed a molten-nitrite method to create lanthanide single-atom catalysts, overcoming previous synthesis limitations due to high reactivity and low reduction potentials. The technique achieves atomic dispersion of multiple lanthanides on diverse substrates—metals, oxides, and carbon—using three key factors: Lux–Flood basicity, mass-diffusion resistance, and molten-salt shielding. A dysprosium-platinum catalyst (Dy₁/Pt) demonstrated superior hydrogen evolution performance, achieving a 20 mV overpotential at −10 mA/cm² in acidic conditions, surpassing commercial Pt/C catalysts. Mechanistic studies reveal molten nitrites enable precise control over atomic isolation, offering a scalable platform for designing high-performance electrocatalysts across various energy applications. This breakthrough establishes molten-salt systems as a versatile synthesis route, potentially accelerating advancements in electrocatalysis for hydrogen production and beyond.
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Nature Materials (2026)Cite this article Lanthanide (Ln) elements have distinctive electronic structures and chemical behaviours that can be used to tune electrocatalytic performance when they are introduced as isolated atomic modifiers. However, their broader use remains limited because their high reactivity and ultralow reduction potentials make it difficult to develop general synthesis strategies that can atomically disperse Ln atoms on diverse substrates. Here we develop a molten-nitrite method that yields Ln single-atom catalysts, permitting the atomic isolation of multiple lanthanides on various supports, including metals, metal oxides and carbon materials. Mechanistic insights obtained from systematic control experiments indicate that Ln single-atom catalyst formation in molten nitrites is dictated by three factors: the Lux–Flood basicity effect, mass-diffusion resistance and molten-salt shielding. As a demonstration, Dy1/Pt shows an overpotential of 20 mV at a current density of −10 mA cm−2 in 0.5-M H2SO4 for acidic hydrogen evolution, which is superior to commercial Pt/C catalysts. This work establishes a framework for synthesizing Ln single-atom catalysts and positions molten-nitrite systems as a versatile platform for electrocatalyst synthesis.This is a preview of subscription content, access via your institution Access Nature and 54 other Nature Portfolio journals Get Nature+, our best-value online-access subscription $32.99 / 30 days cancel any timeSubscribe to this journal Receive 12 print issues and online access $259.00 per yearonly $21.58 per issueBuy this articleUSD 39.95Prices may be subject to local taxes which are calculated during checkoutAll data generated or analysed during this study are included in the article and its Supplementary Information, and are also available from the corresponding author upon request. Source data are provided with this paper.Li, C. et al. Rare earth-based nanomaterials in electrocatalysis. Coord. Chem. Rev. 489, 215204 (2023).Article CAS Google Scholar Lucas, J. et al. Rare earths: science, technology, production and use. MRS Bull. 40, 452–453 (2015).

Google Scholar Wang, X. et al. Embedding oxophilic rare-earth single atom in platinum nanoclusters for efficient hydrogen electro-oxidation. Nat. Commun. 14, 3767 (2023).Article PubMed PubMed Central Google Scholar Feng, J. et al. CO2 electrolysis to multi-carbon products in strong acid at ampere-current levels on La-Cu spheres with channels. Nat. Commun. 15, 4821 (2024).Article CAS PubMed PubMed Central Google Scholar Escudero-Escribano, M. et al. Pt5Gd as a highly active and stable catalyst for oxygen electroreduction. J. Am. Chem. Soc. 134, 16476–16479 (2012).Article CAS PubMed Google Scholar Escudero-Escribano, M. et al. Tuning the activity of Pt alloy electrocatalysts by means of the lanthanide contraction. Science 352, 73–76 (2016).Article CAS PubMed Google Scholar Li, M. et al. Oxophilic Tm-sites in MoS2 trigger thermodynamic spontaneous water dissociation for enhanced hydrogen evolution. Adv. Energy Mater. 14, 2401716 (2024).Article CAS Google Scholar Mao, Q. et al. High-density rare-earth single-atom-triggered unconventional transition of adsorption configuration on La1Pd monatomic alloy metallene for sustainable electrocatalytic alkynol semi-hydrogenation. Adv. Funct. Mater. 34, 2404648 (2024).Article CAS Google Scholar Li, L. et al. Lanthanide-regulating Ru-O covalency optimizes acidic oxygen evolution electrocatalysis. Nat. Commun. 15, 4974 (2024).Article CAS PubMed PubMed Central Google Scholar Zhang, S. et al. Lanthanide electronic perturbation in Pt-Ln (La, Ce, Pr and Nd) alloys for enhanced methanol oxidation reaction activity. Energy Environ. Sci. 14, 5911–5918 (2021).Article CAS Google Scholar Sun, Y. et al. Boosting CO2 electroreduction to C2H4 via unconventional hybridization: high-order Ce4+4f and O2p interaction in Ce-Cu2O for stabilizing Cu+. ACS Nano 17, 13974–13984 (2023).Article CAS PubMed Google Scholar Feng, J. et al. Improving CO2-to-C2+ product electroreduction efficiency via atomic lanthanide dopant-induced tensile-strained CuOx catalysts. J. Am. Chem. Soc. 145, 9857–9866 (2023).Article CAS PubMed Google Scholar Xu, J. et al. Ultrathin 2D rare-earth nanomaterials: compositions, syntheses, and applications. Adv. Mater. 32, 1806461 (2020).Article CAS Google Scholar Hu, Y. et al. Synthesis of Pt-rare earth metal nanoalloys. J. Am. Chem. Soc. 142, 953–961 (2020).Article CAS PubMed Google Scholar Santos, D. M. F. et al. Platinum–rare earth electrodes for hydrogen evolution in alkaline water electrolysis. Int. J. Hydrogen Energy 38, 3137–3145 (2013).Article CAS Google Scholar Hu, Y. et al. Mechanistic insights into the synthesis of platinum–rare earth metal nanoalloys by a solid-state chemical route. Chem. Mater. 33, 535–546 (2021).Article CAS Google Scholar Kanady, J. S. et al. Synthesis of Pt3Y and other early–late intermetallic nanoparticles by way of a molten reducing agent. J. Am. Chem. Soc. 139, 5672–5675 (2017).Article CAS PubMed Google Scholar Jiang, Y. et al. Molten salt synthesis of carbon-supported Pt-rare earth metal nanoalloy catalysts for oxygen reduction reaction. RSC Adv. 12, 4805–4812 (2022).Article CAS PubMed PubMed Central Google Scholar Wang, X., Tang, Y., Lee, J.-M. & Fu, G. Recent advances in rare-earth-based materials for electrocatalysis. Chem. Catal. 2, 967–1008 (2022).CAS Google Scholar Peera, S. G., Lee, T. G. & Sahu, A. K. Pt-rare earth metal alloy/metal oxide catalysts for oxygen reduction and alcohol oxidation reactions: an overview. Sustain. Energ. Fuels 3, 1866–1891 (2019).Article CAS Google Scholar Nitopi, S. et al. Progress and perspectives of electrochemical CO2 reduction on copper in aqueous electrolyte. Chem. Rev. 119, 7610–7672 (2019).Article CAS PubMed Google Scholar Ma, W. et al. Electrocatalytic reduction of CO2 and CO to multi-carbon compounds over Cu-based catalysts. Chem. Soc. Rev. 50, 12897–12914 (2021).Article CAS PubMed Google Scholar Lin, Y. X. et al. Boosting selective nitrogen reduction to ammonia on electron-deficient copper nanoparticles. Nat. Commun. 10, 4380 (2019).Article PubMed PubMed Central Google Scholar Zhang, R. et al. Electrochemical nitrate reduction to ammonia using copper-based electrocatalysts. Next Energy 4, 100125 (2024).Article CAS Google Scholar Li, Y. et al. Advancements in transition bimetal catalysts for electrochemical 5-hydroxymethylfurfural (HMF) oxidation. J. Energy Chem. 98, 24–46 (2024).Article CAS Google Scholar Zheng, T. et al. Copper-catalysed exclusive CO2 to pure formic acid conversion via single-atom alloying. Nat. Nanotechnol. 16, 1386–1393 (2021).Article CAS PubMed Google Scholar Li, J. et al. Selective CO2 electrolysis to CO using isolated antimony alloyed copper. Nat. Commun. 14, 340 (2023).Article CAS PubMed PubMed Central Google Scholar LaMer, V. K. & Dinegar, R. H. Theory, production and mechanism of formation of monodispersed hydrosols. J. Am. Chem. Soc. 72, 4847–4854 (1950).Article CAS Google Scholar Li, T. et al. Low-temperature molten salt synthesis for ligand-free transition metal oxide nanoparticles. ACS Appl. Energy Mater. 3, 3984–3990 (2020).Article CAS Google Scholar Jansons, A. W., Koskela, K. M., Crockett, B. M. & Hutchison, J. E. Transition metal-doped metal oxide nanocrystals: efficient substitutional doping through a continuous growth process. Chem. Mater. 29, 8167–8176 (2017).Article CAS Google Scholar Kerridge, D. H. & Shakir, W. M. Molten lithium nitrate-potassium nitrate eutectic: the reaction of tin(II) chloride. Thermochim. Acta 136, 149–152 (1988).Article CAS Google Scholar Hu, C. et al. Misoriented high-entropy iridium ruthenium oxide for acidic water splitting. Sci. Adv. 9, eadf9144 (2023).Article CAS PubMed PubMed Central Google Scholar Vreeland, E. C. et al. Enhanced nanoparticle size control by extending LaMer’s mechanism. Chem. Mater. 27, 6059–6066 (2015).Article CAS Google Scholar Hayashi, Y., Kimura, T. & Yamaguchi, T. Preparation of rod-shaped BaTiO3 powder. J. Mater. Sci. 21, 757–762 (1986).Article CAS Google Scholar Zhao, D. et al. On the viscosity of molten salts and molten salt mixtures and its temperature dependence. J. Energy Storage 61, 106707 (2023).Article Google Scholar Dash, A., Vaßen, R., Guillon, O. & Gonzalez-Julian, J. Molten salt shielded synthesis of oxidation prone materials in air. Nat. Mater. 18, 465–470 (2019).Article CAS PubMed Google Scholar Dash, A. et al. Synthesis of Ti3SiC2 MAX phase powder by a molten salt shielded synthesis (MS3) method in air. J. Eur. Ceram. Soc. 39, 3651–3659 (2019).Article CAS Google Scholar Dai, Y. et al. The physical chemistry and materials science behind sinter-resistant catalysts. Chem. Soc. Rev. 47, 4314–4331 (2018).Article CAS PubMed Google Scholar Chen, J. et al. Diversity of platinum-sites at platinum/fullerene interface accelerates alkaline hydrogen evolution. Nat. Commun. 14, 1711 (2023).Article CAS PubMed PubMed Central Google Scholar Download referencesC.X. acknowledges the National Key Research and Development Program of China (2024YFB4105700), the Scientific Research Innovation Capability Support Project for Young Faculty (SRICSPYF-ZY2025052), the Natural Science Foundation of Sichuan Province (2025NSFJQ0017) and the University of Electronic Science and Technology of China (ZYGX2025TS001). T.Z. acknowledges NSFC (22278067 and 22322201). X.L. acknowledges NSFC (22475030) and the Natural Science Foundation of Sichuan Province (2024NSFSC1107). Q.J. acknowledges NSFC (22405035) and the Natural Science Foundation of Sichuan Province (2024NSFSC1104). We appreciate the Analysis and Testing Center, University of Electronic Science and Technology of China, for their technical support, especially Y. Hu and J. Li with regard to XRD and HAADF-STEM, respectively. We thank beamline BL11B (31124.02.SSRF.BL11B) of the Shanghai Synchrotron Radiation Facility for providing the beamtime. We appreciate the discussion with C. Guo from SUPCON Technology for the theoretical computations in this work.School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu, People’s Republic of ChinaHaoyuan Wang (王昊元), Chunxiao Liu (刘春晓), Yuan Ji (计远), Hongliang Zeng (曾洪亮), Xinyan Zhang (张昕岩), Qisheng Zeng (曾齐升), Jiawei Li (李嘉伟), Qinglong Gao (高秦龙), Xu Li (李旭), Tingting Zheng (郑婷婷), Qiu Jiang (江秋) & Chuan Xia (夏川)Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, People’s Republic of ChinaHaoyuan Wang (王昊元), Sunpei Hu (胡孙培), Xinyan Zhang (张昕岩), Yao Zhang (张尧) & Jie Zeng (曾杰)Search author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarSearch author on:PubMed Google ScholarThe project was conceptualized and supervised by C.X. H.W. conducted all the experiments with help from the other authors. H.W. carried out all the sample syntheses. H.W., H.Z. and Q.Z. performed the electrochemical tests. S.H. helped with the electron microscopy. H.W., J.L. and X.Z. performed the ex situ measurements. H.W. and Q.G. conducted the X-ray absorption fine structure measurements. C.L., X.L. and Y.Z. helped with the statistical analysis. C.L., X.Z., Q.Z. and J.L. provided useful discussion on this work. J.Z. helped with the design of the mechanism experiments. Y.J. designed the figures in the paper. H.W., C.L., T.Z., Q.J. and C.X. wrote and revised the paper.Correspondence to Chuan Xia (夏川).The authors declare no competing interests.Nature Materials thanks Wolfgang Schmidt, Deli Wang and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.Supplementary Figs. 1–69, Notes 1–13, Tables 1–4, additional methods and safety warning.Atomic coordinates of the optimized computational models used in this work.EXAFS data of Dy1/CuO, Dy1/Cu2O, Dy1/Cu and references plotted in Fig. 1h.Dy1/Pt XRD data plotted in Fig. 3b, Dy1/Rh XRD data plotted in Fig. 3d, Dy1/Ir XRD data plotted in Fig. 3f, EXAFS data of Dy1/Pt, Dy1/Rh, Dy1/Ir and references plotted in Fig. 3g.EXAFS data of Dy1/Y2O3, Dy1/ZnO, Dy1/Pd, Dy1/AlOx, Dy1/RuO2, Dy1/SnO2, Dy1/C, Lu1/Mn3O4 and Lu1/FeOx and references plotted in Fig. 4b.LSV polarization data plotted in Fig. 5a, ECSA-normalized LSV polarization data plotted in Fig. 5b, Tafel slopes plotted in Fig. 5c, stability test data plotted in Fig. 5d and proton exchange membrane chronopotentiometry stability test data plotted in Fig. 5f.Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.Reprints and permissionsWang, H., Liu, C., Ji, Y. et al. A molten-salt dispersion of lanthanides at the atomic scale. Nat. Mater. (2026). https://doi.org/10.1038/s41563-026-02492-yDownload citationReceived: 14 December 2024Accepted: 13 January 2026Published: 19 February 2026Version of record: 19 February 2026DOI: https://doi.org/10.1038/s41563-026-02492-yAnyone you share the following link with will be able to read this content:Sorry, a shareable link is not currently available for this article. Provided by the Springer Nature SharedIt content-sharing initiative

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