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由预先设计的受羊肚菌启发的封装导向的超小钯和钯铂纳米颗粒用于高效催化。

Ultrasmall Pd and PtPd nanoparticles for highly efficient catalysis directed by predesigned Morchella-inspired encapsulation.

作者信息

Li Shunling, Li Lei, Wen Xinwei, Yang Xiaoqiang, Shi Xiaoling, Qu Qing

机构信息

School of Chemical Science and Technology, Yunnan University, Kunming 650091, China.

State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Yunnan University, Kunming 650091, China.

出版信息

J Colloid Interface Sci. 2021 Mar;585:368-375. doi: 10.1016/j.jcis.2020.11.097. Epub 2020 Nov 30.

Abstract

Although bio-inspired designs for ultrasmall metal nanoparticles (NPs) are likely to play an important role in exploring future heterogeneous catalysis materials, synthesizing these structures while retaining surface activity and avoiding aggregation is challenging. Inspired by the Morchella with the spatially and well-organized porous structures, we proposed a biological strategy to yield NPs with ultrasmall and highly dispersed while maintaining high catalytic activity through surfactin self-assembly. Here, multifunctional Morchella-like biological pores (MBP) nanomaterials (28 nm) with reduction and encapsulation has been synthesized by surfactin self-assembly, then, ultrasmall PtPd (2.90 nm) and Pd NPs (~2.87 nm) with coordinated sizes and well-dispersed have been successfully reduced and encapsulated inside the MBP. Notably, the synthesis possesses distinct advantages such as mild reaction conditions, strong controllability, good biological compatibility, low-toxicity and environmental friendliness. The as-prepared MBP-encapsulated ultrasmall PtPd and Pd NPs (M@MBP NPs) exhibited excellent catalytic activity and toxicity resistance for the ethanol oxidation reaction (EOR) in KOH, due to the synergistic effect of MBP and ultrasmall metal NPs. The current density of PtPd@MBP and Pd@MBP NPs were 3.35 and 2.72 A mg, respectively. Such MBP synthesized and encapsulated nanoparticles open a new frontier for the design and preparation of NPs for various applications, such as catalysis, bioremediation and drug delivery.

摘要

尽管受生物启发设计的超小金属纳米颗粒(NPs)可能在探索未来的多相催化材料中发挥重要作用,但在合成这些结构时保持表面活性并避免聚集具有挑战性。受具有空间有序多孔结构的羊肚菌启发,我们提出了一种生物策略,通过表面活性素自组装来制备具有超小尺寸且高度分散同时保持高催化活性的NPs。在此,通过表面活性素自组装合成了具有还原和包封功能的多功能类羊肚菌生物孔(MBP)纳米材料(约28纳米),然后,成功地将尺寸协调且分散良好的超小PtPd(约2.90纳米)和Pd NPs(约2.87纳米)还原并包封在MBP内部。值得注意的是,该合成方法具有反应条件温和、可控性强、生物相容性好、低毒和环境友好等明显优势。所制备的MBP包封的超小PtPd和Pd NPs(M@MBP NPs)由于MBP和超小金属NPs的协同作用,在KOH中对乙醇氧化反应(EOR)表现出优异的催化活性和抗毒性。PtPd@MBP和Pd@MBP NPs的电流密度分别为3.35和2.72 A mg。这种合成并包封纳米颗粒的MBP为设计和制备用于催化、生物修复和药物递送等各种应用领域的NPs开辟了新的前沿。

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