Sarkar Rajib, Graves Lisa S, Taylor Jessie R, Arachchige Indika U
Department of Chemistry, Virginia Commonwealth University, Richmond, Virginia 23284-2006, United States.
ACS Appl Mater Interfaces. 2023 Oct 30. doi: 10.1021/acsami.3c07740.
Assembly of nanoparticles (NPs) into functional macrostructures is imperative for the development of NP-based devices. However, existing methods employ insulating organic ligands, polymers, and biomolecules as mediators for the NP assembly, which are detrimental for charge transport and interparticle coupling that impede the efficient integration of low-dimensional properties. Herein, we report a methodology for the direct self-supported assembly of Ag/Pt/Pd alloy NPs into high surface area (119.1 ± 3.9 to 140.1 ± 5.7 m/g), mesoporous (19.7 ± 6.2 to 23.0 ± 1.6 nm), and conducting nanostructures (aerogels) that show superior electrocatalytic activity and stability in methanol (MOR) and ethanol (EOR) oxidation reactions. Ultrasmall (3.9 ± 1.3 nm) and quasi-spherical Ag/Pt/Pd alloy NPs were synthesized via stepwise galvanic replacement reaction (GRR) of glutathione (GSH)-coated Ag NPs. As-synthesized NPs were transformed into free-standing alloy hydrogels via chemical oxidation of the GSH ligands. The composition of alloy aerogels was tuned by varying the oxidant/thiolate molar ratio of the precursor NP sol that prompts Ag dealloying with in situ generated HNO, selectively enriching the Pt and Pd catalytic sites on the aerogel surface. The highest-performing alloy aerogel (AgPtPd) demonstrates excellent mass activity for methanol (3179.5 mA/mg) and ethanol (2444.5 mA/mg) electro-oxidation reactions, which are ∼4-5 times higher than those of commercial Pt/C and Pd/C electrocatalysts. The aerogel also maintained high alcohol oxidation activity for 17 h at a constant potential of -0.3 V in an alkaline medium. The synergistic effects of noble metal alloying, high surface area and mesoporosity, and the pristine active surface of aerogels provide efficient interaction of analytes with the nanostructure surface, facilitating both MOR and EOR activity and improving tolerance for poisonous byproducts, enabling the Ag/Pt/Pd alloy aerogel a promising (electro)catalyst for a number of new technologies.
将纳米颗粒(NPs)组装成功能性宏观结构对于基于NP的器件的开发至关重要。然而,现有方法采用绝缘有机配体、聚合物和生物分子作为NP组装的介质,这对电荷传输和颗粒间耦合不利,从而阻碍了低维特性的有效整合。在此,我们报告了一种将Ag/Pt/Pd合金NP直接自支撑组装成高表面积(119.1±3.9至140.1±5.7 m/g)、介孔(19.7±6.2至23.0±1.6 nm)且导电的纳米结构(气凝胶)的方法,该气凝胶在甲醇(MOR)和乙醇(EOR)氧化反应中表现出优异的电催化活性和稳定性。通过谷胱甘肽(GSH)包覆的Ag NP的逐步电置换反应(GRR)合成了超小(3.9±1.3 nm)且近似球形的Ag/Pt/Pd合金NP。通过GSH配体的化学氧化将合成的NP转化为独立的合金水凝胶。通过改变前体NP溶胶的氧化剂/硫醇盐摩尔比来调节合金气凝胶的组成,该比例促使Ag脱合金化并原位生成HNO,从而选择性地富集气凝胶表面的Pt和Pd催化位点。性能最佳的合金气凝胶(AgPtPd)在甲醇(3179.5 mA/mg)和乙醇(2444.5 mA/mg)电氧化反应中表现出优异的质量活性,比商业Pt/C和Pd/C电催化剂高出约4-5倍。该气凝胶在碱性介质中于-0.3 V的恒定电位下还能保持17 h的高醇氧化活性。贵金属合金化、高表面积和介孔率以及气凝胶原始活性表面的协同作用提供了分析物与纳米结构表面的有效相互作用,促进了MOR和EOR活性并提高了对有毒副产物的耐受性,使Ag/Pt/Pd合金气凝胶成为许多新技术中有前景的(电)催化剂。