RunPd1 fully-exposed clusters for solvent-free hydrogenation of toluene toward hydrogen storage
Year: 2026
Type: article
Abstract: Liquid organic hydrogen carriers are promising for large-scale and long-distance hydrogen storage and transportation. Considering that renewable hydrogen sources are often decentralized and intermittent, designing a catalyst that is simultaneously cost-effective, room-temperature compatible, and environmentally-friendly remains a significant challenge. This contribution introduce a single Pd 1 assisted fully exposed Ru clusters supported on defective graphene/nanodiamonds hybrid support (Ru n Pd 1 /ND@G) catalyzing efficient toluene hydrogenation under solvent-free conditions, in which the conversion of toluene could achieve 100% even at room temperature. Remarkably, Ru n Pd 1 fully-exposed cluster delivers an exceptionally high turnover frequency of 35199.5 h −1 at the absence of solvent, which is 5.9 times higher than that of the monometallic Ru/ND@G catalyst. The catalyst exhibits maximized atomic efficiency, excellent recyclability and reaction scalability. Combing with theoretical calculations, it is revealed that Pd 1 assisted fully-exposed Ru cluster catalysts promoted H 2 activation and C-H formation as well as improved reactant (product) adsorption (desorption), which all contribute to the superior activity of Ru n Pd 1 fully-exposed clusters. This work offers a practical strategy for efficient hydrogen energy utilization under solvent-free conditions.
Source: Nature Communications
Institutions: Liaoning University, Chinese Academy of Sciences, Institute of Metal Research, Shenyang National Laboratory for Materials Science, Chongqing University, University of Science and Technology of China, The Hong Kong University of Science and Technology (Guangzhou), Peking University, Beijing National Laboratory for Molecular Sciences
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $6,990
OpenAlex ID: W7204109266
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