催化作用
材料科学
铂金
制氢
扫描透射电子显微镜
氢
光致发光
密度泛函理论
铂纳米粒子
氢燃料
吸收(声学)
吸附
分解水
光化学
纳米技术
化学物理
透射电子显微镜
化学工程
纳米颗粒
压电响应力显微镜
顺磁性
电子顺磁共振
作者
Yuming Chen,Yu‐Ching Chen,K. N. Tu,Yi‐Dong Lin,Yan‐Gu Lin,Hsun‐Yen Lin,Samiksha Bajaj,Jyh Ming Wu
出处
期刊:Small
[Wiley]
日期:2025-10-06
卷期号:21 (47): e08162-e08162
被引量:1
标识
DOI:10.1002/smll.202508162
摘要
The advent of single-atom catalysts (SACs) has revolutionized catalysis, delivering outstanding performance in diverse chemical reactions. This study introduces a novel piezoelectric catalytic system employing single-atom platinum-modified MoS2 nanoflowers (NFs) for enhanced hydrogen evolution reactions (HER). High-angle annular dark field scanning transmission electron microscopy (HAADF-STEM) identifies single-atom platinum as bright dots, while X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analyses verify its oxidation state and radial distance. Piezoresponse force microscopy (PFM) confirms increased piezoresponse amplitude due to structural asymmetry from platinum modification. Time-resolved photoluminescence (TRPL) reveals an extended carrier lifetime of 5.7 ns, while the modified catalyst (SA-Pt-01, MoS2 NFs with 1 wt.% Pt) achieves a fourfold increase in hydrogen production efficiency, reaching 2206.15 µmol·g-1·h-1. Notably, SA-Pt-1 generates 7786.9 µmol·g-1 in 12 h, showcasing sustained performance. Electron paramagnetic resonance (EPR) detects stronger •OH radical signals, indicating increased reactive availability. Density functional theory (DFT) simulations show that single-atom Pt incorporation enhances adsorption energy and reduces energy barriers for hydrogen production. These findings underscore the potential of single-atom Pt-modified MoS2 NFs as efficient, sustainable catalysts for clean hydrogen energy applications.
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