Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/140878
Title: Unraveling the cooperative synergy of zero-dimensional graphene quantum dots and metal nanocrystals enabled by layer-by-layer assembly
Authors: Zeng, Zhiping
Xiao, Fang-Xing
Phan, Hung
Chen, Shufen
Yu, Zhongzheng
Wang, Rong
Nguyen, Thuc-Quyen
Tan, Timothy Thatt Yang
Keywords: Engineering::Chemical engineering
Issue Date: 2017
Source: Zeng, Z., Xiao, F.-X., Phan, H., Chen, S., Yu, Z., Wang, R., . . . Tan, T. T. Y. (2018). Unraveling the cooperative synergy of zero-dimensional graphene quantum dots and metal nanocrystals enabled by layer-by-layer assembly. Journal of Materials Chemistry A, 6(4), 1700-1713. doi:10.1039/c7ta09119b
Journal: Journal of Materials Chemistry A
Abstract: Recent years have witnessed a cornucopia of synthetic methods for fabricating carbon–metal nanocomposites. Nonetheless, achieving a cooperative synergy of zero-dimensional carbon nanomaterials and metal nanocrystals is still uncommon. To this end, we performed a controllable structural design comprising customizable alternating layers of active and functional zero-dimensional nanomaterials, which were intimately assembled together. This unique highly-ordered multilayer configuration was afforded by a judicious layer-by-layer (LbL) assembly strategy, enabling the rational and tunable construction of a series of well-defined metal/graphene quantum dots (M/GQDs)n (M = Au, Ag, Pt) multilayers. This strategy allows the direct assembly of customized units of positively-charged graphene quantum dots (GQDs) and negatively-charged metal nanocrystals (NCs), which were integrated in an alternating stacked fashion under a pronounced electrostatic attractive interaction. Moreover, these multilayer thin films demonstrate remarkably efficient and versatile catalytic performance toward the selective organic transformation of aromatic nitro compounds, electrocatalytic methanol oxidation and photoelectrochemical water splitting under simulated solar light irradiation under ambient conditions, attributed to the cooperative synergy of the metal NC and GQD building blocks. More significantly, the catalytic performances of the (M/GQDs)n (M = Au, Ag, Pt) multilayer thin films are tunable via the assembly cycle and sequence, as well as by selecting different metal NC types. This work highlights the significance of the customizable design of GQDs–metal-based systems for various advanced chemical-to-energy conversion applications.
URI: https://hdl.handle.net/10356/140878
ISSN: 2050-7488
DOI: 10.1039/c7ta09119b
Rights: © 2018 The Royal Society of Chemistry. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SCBE Journal Articles

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