DOE PAGES title logo U.S. Department of Energy
Office of Scientific and Technical Information
  1. Polystyrene Hydrogenolysis to High-Quality Lubricants Using Ni/SiO2

    Pyrolytic and light-activated oxidation processes are leading technologies for utilizing polystyrene (PS) wastes. These approaches exhibit poor selectivities, use complex reactors, and require solvents. Hydrogenolysis is effective for deconstructing polyolefins, but its application to PS feedstocks has been limited. Herein, we demonstrate Ni/SiO2 catalysts to facilitate PS (Mw ≈ 97 kDa) hydrogenolysis to produce lubricant base oils possessing group IV properties, achieving maximum yields of 70% within 6 h at 300 °C and 70 bar of H2. Gas, liquid, and oil product yields are stable across reaction conditions, whereas hydrogenation of the PS aromaticity and reduction of the molecular weightmore » benefit from higher temperatures and H2 pressures. Time-dependent experiments underscore the importance of elevated H2 pressure, revealing that PS hydrogenolysis occurs sequentially, with aromatic ring hydrogenation preceding degradation of the C–C backbone. Kinetic measurements with 1,2-diphenylethane as a probe molecule demonstrate that ring hydrogenation pis 3 orders of magnitude faster than internal C–C bond cleavage over Ni/SiO2. Ni/SiO2 proves to be effective in the hydrogenolysis of heavier PS polymers and rigid commercial PS products. Conversely, flexibility and foam PS feeds result in Ni/SiO2 deactivation, attributed to performance additives. Unlike polyolefins, the process produces very little methane and other light hydrocarbons. Furthermore, these findings expand the applicability of hydrogenolysis to PS feedstocks, offering a versatile solution and broadening the range of high-value products from PS to include lubricant base oils.« less
  2. Enhanced sub-bandgap efficiency of a solid-state organic intermediate band solar cell using triplet–triplet annihilation

    Conventional solar cells absorb photons with energy above the bandgap of the active layer while sub-bandgap photons are unharvested. One way to overcome this loss is to capture the low energy light in the triplet state of a molecule capable of undergoing triplet–triplet annihilation (TTA), which pools the energy of two triplet states into one high energy singlet state that can then be utilized. This mechanism underlies the function of an organic intermediate band solar cell (IBSC). Here, we report a solid-state organic IBSC that shows enhanced photocurrent derived from TTA that converts sub-bandgap light into charge carriers. Femtosecond resolutionmore » transient absorption spectroscopy and delayed fluorescence spectroscopy provide evidence for the triplet sensitization and upconversion mechanisms, while external quantum efficiency measurements in the presence of a broadband background light demonstrate that sub-bandgap performance enhancements are achievable in this device. In conclusion, the solid-state architecture introduced in this work serves as an alternative to previously demonstrated solution-based IBSCs, and is a compelling model for future research efforts in this area.« less
  3. Ultrafast Exciton Dissociation and Long-Lived Charge Separation in a Photovoltaic Pentacene–MoS2 van der Waals Heterojunction

    van der Waals heterojunctions between two-dimensional (2D) layered materials and nanomaterials of different dimensions present unique opportunities for gate-tunable optoelectronic devices. Mixed-dimensional p–n heterojunction diodes, such as p-type pentacene (0D) and n-type monolayer MoS2 (2D), are especially interesting for photovoltaic applications where the absorption cross-section and charge transfer processes can be tailored by rational selection from the vast library of organic molecules and 2D materials. In this work, we study the kinetics of excited carriers in pentacene–MoS2 p–n type-II heterojunctions by transient absorption spectroscopy. These measurements show that the dissociation of MoS2 excitons occurs by hole transfer to pentacene onmore » the time scale of 6.7 ps. In addition, the charge-separated state lives for 5.1 ns, up to an order of magnitude longer than the recombination lifetimes from previously reported 2D material heterojunctions. By studying the fractional amplitudes of the MoS2 decay processes, the hole transfer yield from MoS2 to pentacene is found to be ~50%, with the remaining holes undergoing trapping due to surface defects. In general, the ultrafast charge transfer and long-lived charge-separated state in pentacene–MoS2 p–n heterojunctions suggest significant promise for mixed-dimensional van der Waals heterostructures in photovoltaics, photodetectors, and related optoelectronic technologies.« less

Search for:
All Records
Subject
Organic compounds

Refine by:
Article Type
Availability
Journal
Creator / Author
Publication Date
Research Organization