skip to main content


Title: Characterization of Platinum Nanoparticles Utilized in Photocatalytic Hydrogen Synthesis*
As energy needs grow ever greater in today's world, many scientists are investigating possible replacements for fossil fuels as an energy source. The use of hydrogen (H2) gas in particular is undergoing a significant amount of research, but a major obstacle in the use of H2 for green, environmentally-friendly fuel is the energetic and chemical requirement to synthesize the gas. A possibility in satisfying current and future H2 production needs is the use of photocatalytic reactions, where a light-absorbing substance acts as a catalyst in shuttling electrons from a donor to protons that are reduced into H2. Previous research conducted at BYU found such a system where platinum nanoparticles bound to ferritin catalyzed the photoreaction of methyl viologen to reduce protons in an organic acid, which offered a one hundred-fold increase in H2 production efficiency over photocatalytic reactions catalyzed by bulk platinum. We are reporting on our efforts to optimize the synthesis of the platinum nanoparticles bound to ferritin that are used in this photocatalytic system and how we characterize these nanoparticles. *We'd like to thank the Brigham Young University Physics Department and the National Science Foundation (grant no. 1757998) for their generous funding. To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2018.4CS.J03.3  more » « less
Award ID(s):
1757998
NSF-PAR ID:
10106074
Author(s) / Creator(s):
; ;
Date Published:
Journal Name:
Bulletin of the American Physical Society
Volume:
63
Issue:
18
ISSN:
0003-0503
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Hydrogen (H2) gas is a possible alternate fuel to help meet increasing worldwide energy needs, but a major obstacle in the use of H2 for green, environmentally-friendly fuel is the energetic and chemical requirements to synthesize the gas. We are studying the use of photocatalytic reactions to produce H2, where a light-absorbing substance acts as a catalyst in shuttling electrons from a donor to protons that are reduced into H2. Previous research conducted at BYU showed that platinum nanoparticles bound to ferritin catalyzed the photoreaction of methyl viologen to reduce protons in an organic acid offered an increase in hydrogen production efficiency by up to 100 times over platinum black (a commonly available platinum-based catalyst). We are reporting on our efforts to optimize the synthesis of the platinum nanoparticles bound to ferritin that are used in this photocatalytic system and how we characterize these nanoparticles, as well as how these characteristics affect H2 production. *We'd like to thank the Brigham Young University Physics Department and the National Science Foundation (grant no. 1757998) for their generous funding. 
    more » « less
  2. The photocatalytic hydrogen evolution reaction (HER) by water splitting has been studied, using catalysts based on crystalline TiO2 nanowires (TiO2NWs), which were synthesized by a hydrothermal procedure. This nanomaterial was subsequently modified by incorporating different loadings (1%, 3% and 5%) of gold nanoparticles (AuNPs) on the surface, previously exfoliated MoS2 nanosheets, and CeO2 nanoparticles (CeO2NPs). These nanomaterials, as well as the different synthesized catalysts, were characterized by electron microscopy (HR-SEM and HR-TEM), XPS, XRD, Raman, Reflectance and BET surface area. HER studies were performed in aqueous solution, under irradiation at different wavelengths (UV-visible), which were selected through the appropriate use of optical filters. The results obtained show that there is a synergistic effect between the different nanomaterials of the catalysts. The specific area of the catalyst, and especially the increased loading of MoS2 and CeO2NPs in the catalyst substantially improved the H2 production, with values of ca. 1114 μm/hg for the catalyst that had the best efficiency. Recyclability studies showed only a decrease in activity of approx. 7% after 15 cycles of use, possibly due to partial leaching of gold nanoparticles during catalyst use cycles. The results obtained in this research are certainly relevant and open many possibilities regarding the potential use and scaling of these heterostructures in the photocatalytic production of H2 from water. 
    more » « less
  3. The sustainable manufacturing of nanoparticles (NPs) has become critical to reduce life cycle energy use and the associated environmental impact. With the ever-growing production volume, titanium dioxide (TiO2) NPs have been produced through various synthesis routes with differing input materials and reactions, which result in differential reactivity, crystallinity, surface areas, and size distributions. In this study, life cycle assessment is used to analyze and compare the environmental impact of TiO2 NPs produced via seven routes covering physical, chemical, and biological syntheses. The synthesis routes are chosen to represent mainstream NP manufacturing and future trends. Mass-, surface area-, and photocatalytic reactivity-based functional units are selected to evaluate the environmental impact and reflect the corresponding changes. The results show that impact associated with the upstream production of different precursors are dominant for the chemical route. Compared to the chemical route, the physical route requires substantial quantities of supporting gas and high-energy inputs to maintain high temperature; therefore, a higher environmental burden is generated. A high environmental burden is also modeled for the biological route due to the required bacterial culture media. This present study aims to identify the most efficient synthesis route for TiO2 NP production, lower the potential environmental impact, and improve green synthesis and sustainability. 
    more » « less
  4. Amongst many strategies for renewable energy conversion, light-driven water splitting to produce clean H2 represents a promising approach and has attracted increasing attention in recent years. Owing to the multi-electron/multi-proton transfer nature of water splitting, low-cost and competent catalysts are needed. Along the rapid development of metal–organic frameworks (MOFs) during the last two decades or so, MOFs have been recognized as an interesting group of catalysts or catalyst supports for photocatalytic water splitting. The modular synthesis, intrinsically high surface area, tunable porosity, and diverse metal nodes and organic struts of MOFs render them excellent catalyst candidates for photocatalytic water splitting. To date, the application of MOFs and their derivatives as photocatalysts for water splitting has become a burgeoning field. Herein, we showcase several representative MOF-based photocatalytic systems for both H2 and O2 evolution reactions (HER, OER). The design principle of each catalytic system is specifically discussed. The current challenges and opportunities of utilizing MOFs for photocatalytic water splitting are discussed in the end. 
    more » « less
  5. Biological systems convert chemical energy into mechanical work by using protein catalysts that assume kinetically controlled conformational states. Synthetic chemomechanical systems using chemical catalysis have been reported, but they are slow, require high temperatures to operate, or indirectly perform work by harnessing reaction products in liquids (e.g., heat or protons). Here, we introduce a bioinspired chemical strategy for gas-phase chemomechanical transduction that sequences the elementary steps of catalytic reactions on ultrathin (<10 nm) platinum sheets to generate surface stresses that directly drive microactuation (bending radii of 700 nm) at ambient conditions (T = 20 °C; P total = 1 atm). When fueled by hydrogen gas and either oxygen or ozone gas, we show how kinetically controlled surface states of the catalyst can be exploited to achieve fast actuation (600 ms/cycle) at 20 °C. We also show that the approach can integrate photochemically controlled reactions and can be used to drive the reconfiguration of microhinges and complex origami- and kirigami-based microstructures. 
    more » « less