Loof Daniel, Thüringer Oliver, Zielasek Volkmar, Pranti Anmona Shabnam, Lang Walter, Bäumer Marcus
University of Bremen, Institute of Applied and Physical Chemistry Leobener Str. 6 D-28359 Bremen Germany
University of Bremen, Institute for Microsensors, Actuators and Systems (IMSAS) Otto-Hahn-Allee 1 D-28359 Bremen Germany.
Nanoscale Adv. 2024 Jan 31;6(5):1436-1446. doi: 10.1039/d3na00955f. eCollection 2024 Feb 27.
Microporous networks of Pt nanoparticles (NP) interlinked by aromatic diamines have recently shown prospects of application as hydrogen combustion catalysts in H gas microsensors. In particular with respect to long-term sensor performance, they outperformed plain Pt NP as catalysts. In this paper, electron microscopy and Fourier transform infrared (FTIR) spectroscopy data on the stability of -phenylene diamine (PDA) and of the PDA-linked Pt NP network structure during catalyst activation and long-term sensor operation at elevated temperature (up to 120-180 °C) will be presented. For the first time, all data were collected directly from microsensor catalysts, and FTIR was performed , , during activation and sensor operation. While the data confirm high long-term catalyst activity far superior to that of plain Pt NP over 5 days of testing, they reveal that PDA fully decomposed during long-term sensor operation and that the network of discrete Pt nanoparticles changed to a sponge-like Pt nanostructure already during catalyst activation. These findings are at variance with previous work which assumed that stability of the PDA-linked Pt NP network is prerequisite for catalyst stability and performance.
由芳族二胺互连的铂纳米颗粒(NP)微孔网络最近显示出在氢气微传感器中作为氢燃烧催化剂的应用前景。特别是在长期传感器性能方面,它们作为催化剂优于普通的铂纳米颗粒。本文将展示关于在催化剂活化和高温(高达120 - 180°C)下长期传感器运行期间,对苯二胺(PDA)以及PDA连接的铂纳米颗粒网络结构稳定性的电子显微镜和傅里叶变换红外(FTIR)光谱数据。首次直接从微传感器催化剂收集所有数据,并且在活化和传感器运行期间进行了FTIR。虽然数据证实了在5天的测试中,长期催化剂活性远高于普通铂纳米颗粒,但它们表明PDA在长期传感器运行期间完全分解,并且离散铂纳米颗粒网络在催化剂活化期间就已转变为海绵状铂纳米结构。这些发现与先前的工作不同,先前的工作认为PDA连接的铂纳米颗粒网络的稳定性是催化剂稳定性和性能的先决条件。