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Context.One of the most important open questions in planet formation is how dust grains in a protoplanetary disk manage to overcome growth barriers and form the ∼100 km planet building blocks that we call planetesimals. There appears to be a gap between the largest grains that can be produce by coagulation, and the smallest grains that are needed for the streaming instability (SI) to form planetesimals. Aims.Here we explore the novel hypothesis that dust coagulation and the SI work in tandem; in other words, they form a feedback loop where each one boosts the action of the other to bridge the gap between dust grains and planetesimals. Methods.We developed a semi-analytical model of dust concentration due to the SI, and an analytic model of how the SI affects the fragmentation and radial drift barriers. We then combined them to model our proposed feedback loop. Results.In the fragmentation-limited regime, we find a powerful synergy between the SI and dust growth that drastically increases both grain sizes and densities. We find that a midplane dust-to-gas ratio ofϵ ≥ 0.3 is a sufficient condition for the feedback loop to reach the planetesimal-forming region for turbulence values 10⁻⁴ ≤ α ≤ 10⁻³and grain sizes 0.01 ≤ St ≤ 0.1. In contrast, the drift-limited regime only shows grain growth without significant dust accumulation. In other words, planetesimal formation remains challenging in the drift-dominated regime and dust traps may be required to allow planet formation at wide orbital distances. 

Metal-free carbon materials have emerged as cost-effective and high-performance catalysts for the production of hydrogen peroxide (H 2 O 2 ) through the two-electron oxygen reduction reaction (ORR). Here, we show that 3D crumpled graphene with controlled oxygen and defect configurations significantly improves the electrocatalytic production of H 2 O 2 . The crumpled graphene electrocatalyst with optimal defect structures and oxygen functional groups exhibits outstanding H 2 O 2 selectivity of 92–100% in a wide potential window of 0.05–0.7 V vs. reversible hydrogen electrode (RHE) and a high mass activity of 158 A g −1 at 0.65 V vs. RHE in alkaline media. In addition, the crumpled graphene catalyst showed an excellent H 2 O 2 production rate of 473.9 mmol gcat −1 h −1 and stability over 46 h at 0.4 V vs. RHE. Moreover, density functional theory calculations revealed the role of the functional groups and defect sites in the two-electron ORR pathway through the scaling relation between OOH and O adsorption strengths. These results establish a structure-mechanism-performance relationship of functionalized carbon catalysts for the effective production of H 2 O 2 . 

For decades, reports have suggested that photo-catalytic nitrogen fixation by titania in an aqueous environment is possible. Yet a consensus does not exist regarding how the reaction proceeds. Furthermore, the presence of an aqueous protonated solvent and the similarity between the redox potential for nitrogen and proton reduction suggest that ammonia production is unlikely. Here, we re-investigate photo-catalytic nitrogen fixation by titania in an aqueous environment through a series of photo-catalytic and electrocatalytic experiments. Photo-catalytic testing reveals that mineral phase and metal dopants play a marginal role in promoting nitrogen photofixation, with ammonia production increasing when the majority phase is rutile and with iron dopants. However, the presence of a trace amount of adsorbed carbonaceous species increased the rate of ammonia production by two times that observed without adsorbed carbon based species. This suggests that carbon species play a potential larger role in mediating the nitrogen fixation process over mineral phase and metal dopants. We also demonstrate an experimental approach aimed to detect low-level ammonia production from photo-catalysts using rotating ring disk electrode experiments conducted with and without illumination. Consistent with the photocatalysis, ammonia is only discernible at the ring with rutile phase titania, but not with mixed-phase titania. Rotating ring disk electrode experiments may also provide a new avenue to attain a higher degree of precision in detecting ammonia at low levels. 

Abstract Organic materials with redox‐active oxygen functional groups are of great interest as electrode materials for alkali‐ion storage due to their earth‐abundant constituents, structural tunability, and enhanced energy storage properties. Herein, a hybrid carbon framework consisting of reduced graphene oxide and oxygen functionalized carbon quantum dots (CQDs) is developed via the one‐pot solvothermal reduction method, and a systematic study is undertaken to investigate its redox mechanism and electrochemical properties with Li‐, Na‐, and K‐ions. Due to the incorporation of CQDs, the hybrid cathode delivers consistent improvements in charge storage performance for the alkali‐ions and impressive reversible capacity (257 mAh g⁻¹at 50 mA g⁻¹), rate capability (111 mAh g⁻¹at 1 A g⁻¹), and cycling stability (79% retention after 10 000 cycles) with Li‐ion. Furthermore, density functional theory calculations uncover the CQD structure‐electrochemical reactivity trends for different alkali‐ion. The results provide important insights into adopting CQD species for optimal alkali‐ion storage.