Current policies accelerating photovoltaics (PV) deployments are motivated by environmental goals, including reducing greenhouse gas (GHG) emissions by displacing electricity generated from fossil-fuels. Existing practice assesses environmental benefits on a net life-cycle basis, where displaced GHG emissions offset those generated during PV production. However, this approach does not consider that the environmental costs of GHG release during production are incurred early, while environmental benefits accrue later. Thus, where policy targets suggest meeting GHG reduction goals established by a certain date, rapid PV deployment may have counterintuitive, albeit temporary, undesired consequences. On a cumulative radiative forcing (CRF) basis, the environmental improvements attributable to PV might be realized much later than is currently understood, particularly when PV manufacturing utilizes GHG-intensive energy sources (e.g., coal), but deployment occurs in areas with less GHG-intensive electricity sources (e.g., hydroelectric). This paper details a dynamic CRF model to examine the intertemporal warming impacts of PV deployments in California and Wyoming. CRF payback times are longer than GHG payback times by 6-12 years in California and 6-11 years in Wyoming depending on the PV technology mix and deployment strategy. For the same PV capacity being deployed, early installations yield greater CRF benefits (calculated over 10 and 25 years) than installations occurring later in time. Further, CRF benefits are maximized when PV technologies with the lowest manufacturing GHG footprint (cadmium telluride) are deployed in locations with the most GHG-intensive grids (i.e., Wyoming).
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http://dx.doi.org/10.1021/es502542a | DOI Listing |
Environ Pollut
December 2024
Institute of Environment and Sustainable Development, Banaras Hindu University, Varanasi, India; DST-Mahamana Centre of Excellence in Climate Change Research, Banaras Hindu University, Varanasi, India. Electronic address:
Emission estimates of carbon-containing greenhouse gases (CO, CH) and aerosols (PM) were made from forest fire across South Asia using Visible Infrared Imaging Radiometer Suite (VIIRS) based thermal anomalies and fire products. VIIRS 375 m I-band active fire product was selectively retrieved for the years 2012-2021 over forest cover across South Asia. Annual incidence of fire events across South Asia was 0.
View Article and Find Full Text PDFNature
August 2024
Max Planck Institute for Biogeochemistry, Jena, Germany.
J Am Chem Soc
June 2024
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, School of Chemistry and Material Science, Heilongjiang University, Harbin 150080, China.
Near-infrared luminescent rare-earth organic complexes have attracted intensive attention in the field of optical waveguide amplification. However, their optical gains were commonly less than 4 dB/cm due to limited doping concentrations. Herein, two one-dimensional (1D) Nd coordination chains, namely, [Nd(TTA)(DBTDPO)] () and [Nd(TTA)(DPEPO)] (), bridged by phosphine oxide ligands were developed for the neodymium-doped waveguide amplifier.
View Article and Find Full Text PDFGlob Chang Biol
June 2024
Institute of Meteorology and Climate Research, Atmospheric Environmental Research (IMK-IFU), Karlsruhe Institute of Technology (KIT), Garmisch-Partenkirchen, Germany.
Nitrogen oxides (NO) play an important role for atmospheric chemistry and radiative forcing. However, NO emissions from the vast northern circumpolar permafrost regions have not been studied in situ due to limitations of measurement techniques. Our goals were to validate the offline analytical technique, and based on this, to widely quantify in situ NO emissions from peatlands in the southern Eurasian permafrost region.
View Article and Find Full Text PDFNat Commun
June 2024
Department of Civil and Environmental Engineering, 2001 Ghausi Hall, University of California, Davis, 95616, USA.
Rapid decarbonization of the cement industry is critical to meeting climate goals. Oversimplification of direct air capture benefits from hydrated cement carbonation has skewed the ability to derive decarbonization solutions. Here, we present both global cement carbonation magnitude and its dynamic effect on cumulative radiative forcing.
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