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Carbon capture in polymer-based electrolytes

delete2024-04-19
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OA
AI
Y
Yang Wang
T
Tony G. Feric
J
Jing Tang
C
Chao Fang
S
Sara T. Hamilton
D
David M. Halat
B
Bing Wu
H
Hasan Celik
G
Guanhe Rim
T
Tara DuBridge
J
Julianne Oshiro
R
Rui Wang
A
Ah‐Hyung Alissa Park *
J
Jeffrey A. Reimer *
DOI:10.1126/sciadv.adk2350delete
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摘要

摘要

En 中文
Nanoparticle organic hybrid materials (NOHMs) have been proposed as excellent electrolytes for combined CO2 capture and electrochemical conversion due to their conductive nature and chemical tunability. However, CO2 capture behavior and transport properties of these electrolytes after CO2 capture have not yet been studied. Here, we use a variety of nuclear magnetic resonance (NMR) techniques to explore the carbon speciation and transport properties of branched polyethylenimine (PEI) and PEI-grafted silica nanoparticles (denoted as NOHM-I-PEI) after CO2 capture. Quantitative C-13 NMR spectra collected at variable temperatures reveal that absorbed CO2 exists as carbamates (RHNCOO- or RR ' NCOO-) and carbonate/bicarbonate (CO32-/HCO3-). The transport properties of PEI and NOHM-I-PEI studied using H-1 pulsed-field-gradient NMR, combined with molecular dynamics simulations, demonstrate that coulombic interactions between negatively and positively charged chains dominate in PEI, while the self-diffusion in NOHM-I-PEI is dominated by silica nanoparticles. These results provide strategies for selecting adsorbed forms of carbon for electrochemical reduction.
Keyword:
ORGANIC HYBRID MATERIALS
CO2 CAPTURE
MOLECULAR-DYNAMICS
DIOXIDE REACTIONS
LIQUID AMINES
CONVERSION
SOLVENTS
REDUCTION
SYSTEMS
POLYETHYLENIMINE
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Science Advances
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被引数:
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C
Columbia University
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U
University of California Berkeley
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SLAC National Accelerator Laboratory
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University of California System
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