Yun So Yeon, Lee Sangseob, Jin Xiaoyan, Soon Aloysius, Hwang Seong-Ju
Department of Materials Science and Engineering, College of Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Center for Artificial Synesthesia Materials Discovery, Department of Materials Science and Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
Adv Sci (Weinh). 2024 Jun;11(24):e2309819. doi: 10.1002/advs.202309819. Epub 2024 Apr 6.
Exsolution is an effective method for synthesizing robust nanostructured metal-based functional materials. However, no studies have investigated the exsolution of metal nanoparticles into metal nitride substrates. In this study, a versatile nitridation-driven exsolution method is developed for embedding catalytically active metal nanoparticles in conductive metal nitride substrates via the ammonolysis of multimetallic oxides. Using this approach, TiRuO nanowires are phase-transformed into holey TiN nanotubes embedded with exsolved Ru nanoparticles. These Ru-exsolved holey TiN nanotubes exhibit outstanding electrocatalytic activity for the hydrogen evolution reaction with excellent durability, which is significantly higher than that of Ru-deposited TiN nanotubes. The enhanced stability of the Ru-exsolved TiN nanotubes can be attributed to the Ru nanoparticles embedded in the robust metal nitride matrix and the formation of interfacial Ti─N─Ru bonds. Density functional theory calculations reveal that the exsolved Ru nanoparticles have a lower d-band center position and optimized hydrogen affinity than deposited Ru nanoparticles, indicating the superior electrocatalyst performance of the former. In situ Raman spectroscopic analysis reveals that the electron transfer from TiN to Ru nanoparticles is enhanced during the electrocatalytic process. The proposed approach opens a new avenue for stabilizing diverse metal nanostructures in many conductive matrices like metal phosphides and chalcogenides.
析出是合成坚固的纳米结构金属基功能材料的有效方法。然而,尚未有研究调查金属纳米颗粒在金属氮化物基底中的析出情况。在本研究中,开发了一种通用的氮化驱动析出方法,通过多金属氧化物的氨解将催化活性金属纳米颗粒嵌入导电金属氮化物基底中。采用这种方法,TiRuO纳米线相转变为嵌入有析出Ru纳米颗粒的多孔TiN纳米管。这些Ru析出的多孔TiN纳米管对析氢反应表现出优异的电催化活性和出色的耐久性,显著高于Ru沉积的TiN纳米管。Ru析出的TiN纳米管稳定性增强可归因于嵌入坚固金属氮化物基体中的Ru纳米颗粒以及界面Ti─N─Ru键的形成。密度泛函理论计算表明,析出的Ru纳米颗粒比沉积的Ru纳米颗粒具有更低的d带中心位置和优化的氢亲和力,表明前者具有更优异的电催化剂性能。原位拉曼光谱分析表明,在电催化过程中TiN向Ru纳米颗粒的电子转移增强。所提出的方法为在许多导电基体如金属磷化物和硫族化物中稳定各种金属纳米结构开辟了一条新途径。