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Results for “anionic”

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 901 records · Page 50
All sourcesNASA NTRSDOE OSTI
DOE OSTI2025

Doping with phosphorus reduces anion vacancy disorder in CdSeTe semiconductors enabling higher solar cell efficiency

Doping is used in many pn junction devices, such as polycrystalline solar cells, to increase the strength of the junction field to assist charge carrier collection and thus partially mitigate nonradiative recombination losses. We demonstrate a different doping characteristic for inorganic solar cells: using dopants to reduce charge carrier trapping and electronic band tails. Alloying CdTe with Se to form CdSeTe semiconductor reduced recombination, but CdSeTe has more complex defect states which can limit further efficiency gains due to charge carrier trapping and trap-limited mobility. Doping CdSeTe with P (but not N, As, or Sb in this study) reduces band tails (Urbach energies) and lessens the impact of the near valence band trap states, with ambipolar mobilities improving to >50 cm 2 V −1 s −1 , fill factor increasing from 76% to 79%, and efficiencies increasing by 0.9% absolute. Simulations are used to show how such defect reduction improves performance in the radiative limit.

14 SOLAR ENERGY↗
DOE OSTI2018

Nickel–copper supported on a carbon black hydrogen oxidation catalyst integrated into an anion-exchange membrane fuel cell

This work introduces the first practical platinum group metal-free (PGM-free) electrocatalyst for hydrogen oxidation reaction (HOR) in alkaline membrane fuel cells (AMFC), based on nickel-rich Ni 95 Cu 5 -alloy nanoparticles supported on Ketjenblack (KB) family carbon blacks. The catalyst synthesis is scalable and results in expected true alloy of NiCu, which is thoroughly characterized by XRD, microscopy and XPS. Reactivity of the catalyst towards HOR is studied by cyclic voltammetry and explained in view of its composition and structure. This catalyst showed highest specific activity compared to previously reported NiCu electrocatalysts and was successfully integrated into an AMFC membrane electrode assembly (MEA) using commercially available state-of-the-art membrane and ionomer. Single MEA fuel cell tests have demonstrated power density of 350 mWcm -2 at 80°C, which sets a technical record for a PGM-free anode in realistic operating conditions. The MEA with NiCu/KB anode catalysts layer were evaluated by in situ nano- and operando micro-X-ray computed tomography (CT) and results suggest that the nickel state in NiCu is hydrophobic in nature, where the NiCu surface may be isostructural with β-Ni(OH) 2 . The hydrophobic nature of electrocatalyst allows for improved water distribution in MEA and overall fuel cell as observed with operando micro X-ray CT.

25 ENERGY STORAGE↗
DOE OSTI2021

Hydrophilic and hydrophobic carboxamide pincers as anion hosts

Hydrophobic and hydrophilic, monotopic and ditopic carboxamide pincer hosts containing ethyl, hexyl, 2-hydroxyethyl and 2-hydroxyethyl ethyl ether pendant arms were synthesized. Solubility trends indicated that solubilities in water or hydrocarbon solvents varied depending on the nature of the pendant arms. Binding constants for hydrophilic pincers were larger in general than their hydrophobic analogs. Furthermore, significant synergistic binding effects for the ditopic hosts were not observed.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2022

Anion-induced disproportionation of Th( iii ) complexes to form Th( ii ) and Th( iv ) products

Here, a new synthesis of Th(II) complexes has been identified involving addition of simple MX salts (M = Li, Na, K; X = H, Cl, Me, N 3 ) to Cp" 3 Th III [Cp" = [C 5 H 3 (SiMe 3 ) 2 ] in the presence of 18-crown-6 or 2.2.2-cryptand, forming [M(chelate)][Cp" 3 Th II ] and Cp'' 3 Th IV X. Cp tet 3 Th III (Cp tet = C 5 Me 4 H) reacts with KH to form Cp tet 3 Th IV H and the C–H bond activation product, [K(crypt)]{[Cp tet 2 Th IV H[η 1 :η 5 -C 5 Me 3 H(CH 2 )]}.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗