Stable yolk-structured catalysts towards aqueous levulinic acid hydrogenation within a single Ru nanoparticle anchored inside the mesoporous shell of hollow carbon spheres

[Display omitted] To well address the problem of low stability for Ru-based catalysts against sintering and leaching during synthesis and aqueous levulinic acid (LA) hydrogenation to γ-valerolactone (GVL), herein we demonstrate an “inside-to-outside” synthetic strategy for robust yolk-structured nan...

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Bibliographic Details
Published in:Journal of colloid and interface science 2020-09, Vol.576 (C), p.394-403
Main Authors: Yang, Ying, Zhang, Suoying, Gu, Lin, Shao, Shuai, Li, Wei, Zeng, Dehong, Yang, Feng, Hao, Shijie
Format: Article
Language:English
Subjects:
Mesoporous carbon
Ruthenium nanocatalyst
Stability
Yolk-structure
γ-Valerolactone
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Summary:[Display omitted] To well address the problem of low stability for Ru-based catalysts against sintering and leaching during synthesis and aqueous levulinic acid (LA) hydrogenation to γ-valerolactone (GVL), herein we demonstrate an “inside-to-outside” synthetic strategy for robust yolk-structured nanospheres within a single Ru nanoparticle (NP, 4.2 nm) anchored inside the mesoporous shell (pore size, 4.0 nm), denoted as YS Ru@HMCS (yolk-structured Ru encapsulated into hollow mesoporous carbon sphere). Such a shell-supported-core configuration combines the merits of conventional yolk-structured and supported types, in which the active core is not only fully exposed, but also strongly anchored on the shell, based on the optimized interaction between oxidized Ru NP and N-doped mesoporous carbon shell. As a consequence, the resultant YS Ru@HMCS, delivers a high LA conversion (99.4%), a large selectivity to GVL (99.9%), and prolonged cycling life (up to 9 cycles) under water towards the LA hydrogenation, that exceeds conventional yolk-structured and supported analogues. Sintering-resistant, a single Ru NP is successfully encapsulated, and its leaching-resistant property is enhanced based on the improved metal-support contact, thus affording a highly stable Ru catalyst. Moreover, such a synthetic concept can be extended to the stabilization of other supported catalysts, providing a general approach to enhancing both the thermal and chemical stability of supported nanocatalysts.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2020.05.039