Nanoconfinement facilitates reactions of carbon dioxide in supercritical water
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作者:
Nore Stolte
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机构:Hong Kong University of Science and Technology,Department of Physics
Nore Stolte
Rui Hou
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机构:Hong Kong University of Science and Technology,Department of Physics
Rui Hou
Ding Pan
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机构:Hong Kong University of Science and Technology,Department of Physics
Ding Pan
机构:
[1] Hong Kong University of Science and Technology,Department of Physics
[2] HKUST Shenzhen-Hong Kong Collaborative Innovation Research Institute,Department of Chemistry
[3] Hong Kong University of Science and Technology,undefined
[4] Lehrstuhl für Theoretische Chemie,undefined
[5] Ruhr-Universität Bochum,undefined
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Nature Communications
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13卷
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摘要:
The reactions of CO2 in water under extreme pressure-temperature conditions are of great importance to the carbon storage and transport below Earth’s surface, which substantially affect the carbon budget in the atmosphere. Previous studies focus on the CO2(aq) solutions in the bulk phase, but underground aqueous solutions are often confined to the nanoscale, and nanoconfinement and solid-liquid interfaces may substantially affect chemical speciation and reaction mechanisms, which are poorly known on the molecular scale. Here, we apply extensive ab initio molecular dynamics simulations to study aqueous carbon solutions nanoconfined by graphene and stishovite (SiO2) at 10 GPa and 1000 ~ 1400 K. We find that CO2(aq) reacts more in nanoconfinement than in bulk. The stishovite-water interface makes the solutions more acidic, which shifts the chemical equilibria, and the interface chemistry also significantly affects the reaction mechanisms. Our findings suggest that CO2(aq) in deep Earth is more active than previously thought, and confining CO2 and water in nanopores may enhance the efficiency of mineral carbonation.
机构:
Hong Kong Univ Sci & Technol, Dept Phys, Hong Kong, Peoples R China
Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, GermanyHong Kong Univ Sci & Technol, Dept Phys, Hong Kong, Peoples R China
Stolte, Nore
Hou, Rui
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机构:
Hong Kong Univ Sci & Technol, Dept Phys, Hong Kong, Peoples R China
HKUST Shenzhen Hong Kong Collaborat Innovat Res I, Shenzhen, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Phys, Hong Kong, Peoples R China
Hou, Rui
Pan, Ding
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机构:
Hong Kong Univ Sci & Technol, Dept Phys, Hong Kong, Peoples R China
HKUST Shenzhen Hong Kong Collaborat Innovat Res I, Shenzhen, Peoples R China
Hong Kong Univ Sci & Technol, Dept Chem, Hong Kong, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Phys, Hong Kong, Peoples R China
机构:
S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 610540, Guangdong, Peoples R ChinaS China Univ Technol, Sch Chem & Chem Engn, Guangzhou 610540, Guangdong, Peoples R China
Qi Chaorong
Jiang Huanfeng
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S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 610540, Guangdong, Peoples R ChinaS China Univ Technol, Sch Chem & Chem Engn, Guangzhou 610540, Guangdong, Peoples R China