4.8 Article

Construction of New Active Sites: Cu Substitution Enabled Surface Frustrated Lewis Pairs over Calcium Hydroxyapatite for CO2 Hydrogenation

Journal

ADVANCED SCIENCE
Volume 8, Issue 17, Pages -

Publisher

WILEY
DOI: 10.1002/advs.202101382

Keywords

copper; gas-phase reactions; hydroxyapatite; surface chemistry; surface frustrated Lewis pair

Funding

  1. Ontario Ministry of Research Innovation (MRI)
  2. Ministry of Economic Development, Employment and Infrastructure (MEDI)
  3. Ministry of the Environment and Climate Change (MOECC)
  4. Ministry of Research Innovation, Low Carbon Innovation Fund (LCIF)
  5. Connaught Innovation Fund
  6. Connaught Global Challenge Fund
  7. Natural Sciences and Engineering Research Council of Canada (NSERC)
  8. University Development Fund [UDF01001721]
  9. Program for Guangdong Introducing Innovative and Entrepreneurial Teams [2019ZT08L101]
  10. Anyang Normal University Cultivation Fund [AYNUKPY-2019-11]
  11. University Innovation Fund [S202010479011]

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The study explored the use of isomorphic substitution to create new analogs of molecular surface frustrated Lewis pairs (SFLPs) in CuxCa10-x(PO4)6(OH)2, enhancing its performance in heterogeneous CO2 photocatalytic hydrogenation. The characterized SFLPs were found to have proximal Lewis acidic Cu2+ and Lewis basic OH- characteristics, and the photocatalytic pathway proceeds through a formate reaction intermediate.
Calcium hydroxyphosphate, Ca-10(PO4)(6)(OH)(2), is commonly known as hydroxyapatite (HAP). The acidic calcium and basic phosphate/hydroxide sites in HAP can be modified via isomorphous substitution of calcium and/or hydroxide ions to enable a cornucopia of catalyzed reactions. Herein, isomorphic substitution of Ca2+ ions by Cu2+ ions especially at very low levels of exchange created new analogs of molecular surface frustrated Lewis pairs (SFLPs) in CuxCa10-x(PO4)(6)(OH)(2), thereby boosting its performance metrics in heterogeneous CO2 photocatalytic hydrogenation. In situ Fourier transform infrared spectroscopy characterization and density functional theory calculations provided fundamental insights into the catalytically active SFLPs defined as proximal Lewis acidic Cu2+ and Lewis basic OH-. The photocatalytic pathway proceeds through a formate reaction intermediate, which is generated by the reaction of CO2 with heterolytically dissociated H-2 on the SFLPs. Given the wealth of information thus uncovered, it is highly likely that this work will spur the further development of similar classes of materials, leading to the advancement and, ultimately, large-scale application of photocatalytic CO2 reduction technologies.

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