Pacific Northwest National Laboratory

About: Pacific Northwest National Laboratory is a facility organization based out in Richland, Washington, United States. It is known for research contribution in the topics: Catalysis & Aerosol. The organization has 11581 authors who have published 27934 publications receiving 1120489 citations. The organization is also known as: PNL & PNNL.

Reducing emissions from agriculture to meet the 2 °C target

Abstract: More than 100 countries pledged to reduce agricultural greenhouse gas (GHG) emissions in the 2015 Paris Agreement of the United Nations Framework Convention on Climate Change. Yet technical information about how much mitigation is needed in the sector vs. how much is feasible remains poor. We identify a preliminary global target for reducing emissions from agriculture of ~1 GtCO2e yr−1 by 2030 to limit warming in 2100 to 2 °C above pre-industrial levels. Yet plausible agricultural development pathways with mitigation cobenefits deliver only 21–40% of needed mitigation. The target indicates that more transformative technical and policy options will be needed, such as methane inhibitors and finance for new practices. A more comprehensive target for the 2 °C limit should be developed to include soil carbon and agriculture-related mitigation options. Excluding agricultural emissions from mitigation targets and plans will increase the cost of mitigation in other sectors or reduce the feasibility of meeting the 2 °C limit.

Injection of oxygen vacancies in the bulk lattice of layered cathodes

Abstract: Surfaces, interfaces and grain boundaries are classically known to be sinks of defects generated within the bulk lattice. Here, we report an inverse case by which the defects generated at the particle surface are continuously pumped into the bulk lattice. We show that, during operation of a rechargeable battery, oxygen vacancies produced at the surfaces of lithium-rich layered cathode particles migrate towards the inside lattice. This process is associated with a high cutoff voltage at which an anionic redox process is activated. First-principle calculations reveal that triggering of this redox process leads to a sharp decrease of both the formation energy of oxygen vacancies and the migration barrier of oxidized oxide ions, therefore enabling the migration of oxygen vacancies into the bulk lattice of the cathode. This work unveils a coupled redox dynamic that needs to be taken into account when designing high-capacity layered cathode materials for high-voltage lithium-ion batteries.

Pushing the limit of layered transition metal oxide cathodes for high-energy density rechargeable Li ion batteries

Abstract: Development of advanced high energy density lithium ion batteries is important for promoting electromobility. Making electric vehicles attractive and competitive compared to conventional automobiles depends on the availability of reliable, safe, high power, and highly energetic batteries whose components are abundant and cost effective. Nickel rich Li[NixCoyMn1−x−y]O2 layered cathode materials (x > 0.5) are of interest because they can provide very high specific capacity without pushing charging potentials to levels that oxidize the electrolyte solutions. However, these cathode materials suffer from stability problems. We discovered that doping these materials with tungsten (1 mol%) remarkably increases their stability due to a partial layered to cubic (rock salt) phase transition. We demonstrate herein highly stable Li ion battery prototypes consisting of tungsten-stabilized Ni rich cathode materials (x > 0.9) with specific capacities >220 mA h g-1. This development can increase the energy density of Li ion batteries more than 30% above the state of the art without compromising durability.

The fertilizing role of African dust in the Amazon rainforest: A first multiyear assessment based on data from Cloud‐Aerosol Lidar and Infrared Pathfinder Satellite Observations

Abstract: The productivity of the Amazon rainforest is constrained by the availability of nutrients, in particular phosphorus (P). Deposition of long-range transported African dust is recognized as a potentially important but poorly quantified source of phosphorus. This study provides a first multiyear satellite-based estimate of dust deposition into the Amazon Basin using three-dimensional (3-D) aerosol measurements over 2007–2013 from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP). The 7 year average of dust deposition into the Amazon Basin is estimated to be 28 (8–48) Tg a−1 or 29 (8–50) kg ha−1 a−1. The dust deposition shows significant interannual variation that is negatively correlated with the prior-year rainfall in the Sahel. The CALIOP-based multiyear mean estimate of dust deposition matches better with estimates from in situ measurements and model simulations than a previous satellite-based estimate does. The closer agreement benefits from a more realistic geographic definition of the Amazon Basin and inclusion of meridional dust transport calculation in addition to the 3-D nature of CALIOP aerosol measurements. The imported dust could provide about 0.022 (0.006–0.037) Tg P of phosphorus per year, equivalent to 23 (7–39) g P ha−1 a−1 to fertilize the Amazon rainforest. This out-of-basin phosphorus input is comparable to the hydrological loss of phosphorus from the basin, suggesting an important role of African dust in preventing phosphorus depletion on timescales of decades to centuries.

Investigation of the Mechanism of Mg Insertion in Birnessite in Nonaqueous and Aqueous Rechargeable Mg-Ion Batteries

Abstract: Magnesium batteries are an energy storage system that potentially offers high energy density, but development of new high voltage cathode materials and understanding of their electrochemical mechanism are critical to realize its benefits. Herein, we synthesize the layered MnO2 polymorph (the birnessite phase) as a nanostructured phase supported on conductive carbon cloth and compare its electrochemistry and structural changes when it is cycled as a positive electrode material in a Mg-ion battery under nonaqueous or aqueous conditions. X-ray photoelectron spectroscopy and transmission electron microscopy studies show that a conversion mechanism takes place during cycling in a nonaqueous electrolyte, with the formation of MnOOH, MnO, and Mg(OH)2 upon discharge. In aqueous cells, on the other hand, intercalation of Mg2+ ions takes place, accompanied by expulsion of interlayer water and transformation to a spinel-like phase as evidenced by X-ray diffraction. Both systems are structurally quasireversible. The ...