Alexander C. Forse

Research interests

Publications

• Structural disorder determines capacitance in nanoporous carbons

  Science · 2024 · 10.1126/science.adn6242

• Raman Spectroscopy Measurements Support Disorder-Driven Capacitance in Nanoporous Carbons

  Journal of the American Chemical Society · 2024 · 10.1021/jacs.4c10214

• High-Capacity, Cooperative CO 2 Capture in a Diamine-Appended Metal–Organic Framework through a Combined Chemisorptive and Physisorptive Mechanism

  Journal of the American Chemical Society · 2024 · 10.1021/jacs.3c13381

• Capturing carbon dioxide from air with charged-sorbents

  Nature · 2024 · 10.1038/s41586-024-07449-2

• Metal–Organic Framework Supercapacitors: Challenges and Opportunities

  Advanced Functional Materials · 2023 · 10.1002/adfm.202308497

• Solvent-derived defects suppress adsorption in MOF-74

  Nature Communications · 2023 · 10.1038/s41467-023-38155-8

• Densified HKUST-1 Monoliths as a Route to High Volumetric and Gravimetric Hydrogen Storage Capacity

  Journal of the American Chemical Society · 2022 · 10.1021/jacs.2c04608

• Selective nitrogen adsorption via backbonding in a metal–organic framework with exposed vanadium sites

  Nature Materials · 2020 · 10.1038/s41563-019-0597-8

• Cooperative carbon capture and steam regeneration with tetraamine-appended metal–organic frameworks

  Science · 2020 · 10.1126/science.abb3976

• Water Enables Efficient CO2 Capture from Natural Gas Flue Emissions in an Oxidation-Resistant Diamine-Appended Metal–Organic Framework

  Journal of the American Chemical Society · 2019 · 10.1021/jacs.9b05567

• Elucidating CO 2 Chemisorption in Diamine-Appended Metal–Organic Frameworks

  Journal of the American Chemical Society · 2018 · 10.1021/jacs.8b10203

• Enantioselective Recognition of Ammonium Carbamates in a Chiral Metal–Organic Framework

  Journal of the American Chemical Society · 2017 · 10.1021/jacs.7b09983

• Direct observation of ion dynamics in supercapacitor electrodes using in situ diffusion NMR spectroscopy

  Nature Energy · 2017 · 10.1038/nenergy.2016.216

• Metal–Organic Nanosheets Formed via Defect-Mediated Transformation of a Hafnium Metal–Organic Framework

  Journal of the American Chemical Society · 2017 · 10.1021/jacs.7b00106

• A Diaminopropane-Appended Metal–Organic Framework Enabling Efficient CO 2 Capture from Coal Flue Gas via a Mixed Adsorption Mechanism

  Journal of the American Chemical Society · 2017 · 10.1021/jacs.7b07612

• How Strong Is the Hydrogen Bond in Hybrid Perovskites?

  The Journal of Physical Chemistry Letters · 2017 · 10.1021/acs.jpclett.7b03106

• NMR reveals the surface functionalisation of Ti 3 C 2 MXene

  Physical Chemistry Chemical Physics · 2016 · https://doi.org/10.1039/c6cp00330c

• High-Rate Intercalation without Nanostructuring in Metastable Nb2O5 Bronze Phases

  Journal of the American Chemical Society · 2016 · 10.1021/jacs.6b04345

• New Perspectives on the Charging Mechanisms of Supercapacitors

  Journal of the American Chemical Society · 2016 · https://doi.org/10.1021/jacs.6b02115

• In situ NMR and electrochemical quartz crystal microbalance techniques reveal the structure of the electrical double layer in supercapacitors

  Nature Materials · 2015 · 10.1038/nmat4318

• NMR Study of Ion Dynamics and Charge Storage in Ionic Liquid Supercapacitors

  Journal of the American Chemical Society · 2015 · 10.1021/jacs.5b03958

• New Insights into the Structure of Nanoporous Carbons from NMR, Raman, and Pair Distribution Function Analysis

  Chemistry of Materials · 2015 · 10.1021/acs.chemmater.5b03216

• Ion counting in supercapacitor electrodes using NMR spectroscopy

  Faraday Discussions · 2014 · 10.1039/c4fd00138a

• Ring Current Effects: Factors Affecting the NMR Chemical Shift of Molecules Adsorbed on Porous Carbons

  The Journal of Physical Chemistry C · 2014 · 10.1021/jp502387x

• In Situ NMR Spectroscopy of Supercapacitors: Insight into the Charge Storage Mechanism

  Journal of the American Chemical Society · 2013 · 10.1021/ja410287s

Current projects

No projects listed.