اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدEffect of Di-phenyl Siloxane on the Catalytic Activity of Pt on Carbon
62
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
The effect of silicone on the catalytic activity of Pt for oxygen reduction and hydrogen adsorption was studied using di-phenyl siloxane as a source compound at a rotating disc electrode (RDE). Di-phenyl siloxane did not affect the catalytic activity of Pt when it was injected into the electrolyte. However, it blocked the oxygen reduction reaction when it was premixed with the catalyst. Proton transport was not blocked in either case. We postulate that di-phenyl siloxane induces hydrophobicity and causes local water starvation thereby blocking oxygen transport. Hence, the slow leaching of silicone seals in a fuel cell could cause silicon accumulation in the electrode, which will irreversibly degrade fuel cell performance by blocking oxygen transport to the catalyst sites.
قيم البحث
اقرأ أيضاً
Understanding the role of elastic strain in modifying catalytic reaction rates is crucial for catalyst design, but experimentally, this effect is often coupled with a ligand effect. To isolate the strain effect, we have investigated the influence of
externally applied elastic strain on the catalytic activity of metal films towards the hydrogen evolution reaction (HER). We show that elastic strain tunes the catalytic activity in a controlled and predictable way. Both theory and experiment show strain controls reactivity in a controlled manner consistent with the qualitative predictions of the HER volcano plot and the d-band theory: Ni and Pt activity were accelerated by compression, while Cu activity was accelerated by tension. By isolating the elastic strain effect from the ligand effect, this study provides a greater insight into the role of elastic strain in controlling electrocatalytic activity.
Previous studies indicate that the properties of graphene oxide (GO) can be significantly improved by enhancing its graphitic domain size through thermal diffusion and clustering of functional groups. Remarkably, this transition takes place below the
decomposition temperature of the functional groups and thus allows fine-tuning of graphitic domains without compromising with the functionality of GO. By studying the transformation of GO under mild thermal treatment, we directly observe this size enhancement of graphitic domains from originally 40 nm2 to 200 nm2 through an extensive transmission electron microscopy (TEM) study. Additionally, we confirm the integrity of the functional groups during this process by comprehensive chemical analysis. A closer look into the process confirms the theoretically predicted relevance for the room temperature stability of GO. We further investigate the influence of enlarged graphitic domains on the hydration behaviour of GO and catalytic performance of single-atom catalysts supported by GO.
In recent years, the immiscible polymer blend system has attracted much attention as the matrix of nanocomposites. Herein, from the perspective of dynamics, the control of the carbon nanotubes (CNTs) migration aided with the interface of polystyrene
(PS) and poly(methyl methacrylate) (PMMA) blends was achieved through a facile melt mixing method. Thus, we revealed a comprehensive relationship between several typical CNTs migrating scenarios and the microwave dielectric properties of their nanocomposites. Based on the unique morphologies and phase domain structures of the immiscible matrix, we further investigated the multiple microwave dielectric relaxation processes and shed new light on the relation between relaxation peak position and the phase domain size distribution. Moreover, by integrating the CNTs interface localization control with the matrix co-continuous structure construction, we found that the interface promotes double percolation effect to achieve conductive percolation at low CNTs loading (~1.06 vol%). Overall, the present study provides a unique nanocomposite material design symphonizing both functional fillers dispersion and location as well as the matrix architecture optimization for microwave applications.
We have investigated the growth of Pt on Ge(110) using scanning tunneling microscopy and spectroscopy. The deposition of several monolayers of Pt on Ge(110) followed by annealing at 1100 K results in the formation of three-dimensional metallic Pt-Ge
nanocrystals. The outermost layer of these crystals exhibits a honeycomb structure. The honeycomb structure is composed of two hexagonal sub-lattices that are displaced vertically by 0.2 {AA} with respect to each other. The nearest-neighbor distance of the atoms in the honeycomb lattice is 2.5${pm}$0.1 {AA}, i.e. very close to the predicted nearest-neighbor distance in germanene (2.4 {AA}). Scanning tunneling spectroscopy reveals that the atomic layer underneath the honeycomb layer is more metallic than the honeycomb layer itself. These observations are in line with a model recently proposed for metal di-(silicides/)germanides: a hexagonal crystal with metal layers separated by semiconductor layers with a honeycomb lattice. Based on our observations we propose that the outermost layer of the Ge2Pt nanocrystal is a germanene layer.
The oxygen reduction (ORR) and oxygen evolution reactions (OER) in Zn-air batteries (ZABs) require highly efficient, cost-effective and stable electrocatalysts as replacements to traditionally high cost, inconsistently stable and low poison resistant
Platinum group metals (PGM) catalysts. Although, nitrogen-doped carbon nanotube (NCNT) arrays have been developed over recent decades through various advanced technologies are now capable of catalyzing ORR efficiently, their underdeveloped bifunctional property, hydrophobic surface, and detrimental preparation strategy are found to limit practical large-scale commercialization for effective rechargeable ZABs. Here, we have demonstrated fabrication of a three-dimensional (3D) nickel foam supported NCNT arrays with CoNi nanoparticles (NPs) encapsulated within the apical domain (denoted as CoNi@NCNT/NF) that exhibits excellent bifunctional catalytic performance toward both ORR (onset potential of 0.97 V vs. RHE) and OER (overpotential of 1.54 V vs. RHE at 10 mA cm$^{-2}$). We further examined the practicability of this CoNi@NCNT/NF material being used as an air electrode for rechargeable ZAB coin cell and pouch cell systems. The ZAB coin cell showed a peak power density of 108 mW cm$^{-2}$ with an energy density of 845 Wh kg$_{Zn}^{-1}$ and robust rechargeability over 28h under ambient conditions, which exceeds the performance of PGM catalysts and leading non-PGM electrocatalysts. In addition, density functional theory (DFT) calculations revealed that the ORR and OER catalytic performance of the CoNi@NCNT/NF electrode are mainly derived from the d-orbitals from the CoNi NPs encapsulated within the apical dominant end of the NCNTs.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
