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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 559 records · Page 31
All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

Designing Nanoplatelet Alloy/Nafion Catalytic Interface for Optimization of PEMFCs: Performance, Durability, and CO Resistance

We have adapted the two phase Brust method to synthesize large quantities of AuPd alloy nanoparticles with diameter of 1.86 ± 0.40 nm. When the particles were spread at the air water interface of a Langmuir Blodgett (LB) trough, they exhibited a distinct pressure area isotherm curve. The X-ray reflectivity (XRR) shows the formation of an incompressible monolayer with uniform thickness of 1.16 ± 0.02 nm at low pressures which collapses to form a second layer with 2.13 nm thick at higher pressures. High resolution transmission electron microscopy (HRTEM) imaging of the monolayer indicates that the particles are highly crystalline, with well-defined atomic planes and self-assembly into a hexagonal structure. Extended X-ray absorption fine structure (EXAFS) analysis of the LB lift-off films only shows Au-Au and Au-Pd configurations, consistent with the formation of random alloy rather than core shell structure. When the particle monolayer was lifted onto the Nafion membrane of a proton exchange membrane fuel cell (PEMFC), a maximum power output of 0.54 W/cm 2 was obtained with a Pt loading of only 0.15 mg/cm 2 and 0.05 mg/cm 2 at the cathode and anode, respectively. This represents a 15% enhancement, which persists even after 30k cycles, relative to a membrane electrode assembly (MEA) using a non-coated membrane. Density function theory (DFT) modeling of the hexagonally packed platelet nanoparticle alloy structure deposited on Nafion predicted that the SO 3 functionality serves a similar function to metal oxide supports in reducing the activation barrier for the CO oxidation reaction. This was confirmed by measuring the power output of a PEMFC when 0.1% CO was mixed either into the input H 2 stream at the anode or with O 2 at the cathode. In the uncoated MEAs, a significant decrease of 72% and 61% was measured when CO was introduced at the anode and cathode, respectively, while MEAs with coated particle membranes only experienced a decrease of 21% and 17%, respectively. These results indicate that a synergy can be established between the nanoparticle platelets and the surface of the Nafion membrane which can produce CO resistant PEMFC that could operate at ambient temperatures on impure, but abundant hydrogen gas such as those produced by reformate or electrolysis processes. Furthermore the availability of inexpensive H 2 opens opportunities for gas distribution and greatly facilitates the commercialization of PEMFCs, which will conform to the ambitious goals set by the Department of Energy (DOE) for 2020.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Optimal Pre-hydration Age for CO 2 Sequestration through Portland Cement Carbonation

An emerging technology of CO 2 sequestration in Portland cement (PC) is through accelerated carbonation, where PC is intentionally carbonated at early hydration age and reinitiates long-term hydration upon completion of carbonation. However, the current literature has overlooked a fact that different PC hydration ages prior to carbonation (pre-hydration) could lead to distinct carbonation efficiencies and subsequent hydration behaviors (post-hydration). Here, we examine the effects of length of pre-hydration period on CO 2 uptake and on the hydration extent and final strength at 28 days. The CO 2 and H 2 O profiles in the carbonated PC were examined with thermogravimetric analysis/derivative thermogravimetric analysis. The pre-hydration path was traced with isothermal calorimetry. Experimental results suggested that extension of pre-hydration decreased CO 2 uptake, but enhanced the extent of PC hydration at 28 days. It was found that a pre-hydration beyond the late deceleration period of PC hydration (where heat generation is slowing down) led to a higher hydrate content of cement paste, hence forming a higher compressive strength of mortar compared to the noncarbonated benchmarks at 28 days. The lesser carbonation-induced water loss and the nucleation seeding enabled by calcium carbonate are likely responsible for this effect. Furthermore, the finding reported here should be useful for fine tuning PC carbonation process for CO 2 sequestration in concrete.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗