“…Specifically, the ligand chains form a hydrophobic domain around the pocket that facilitates the diffusion of CO 2 , while inhibiting the diffusion of water/protons, into the NOLI structure, favouring CO 2 conversion over the HER. 192 The Ag–NOLI improved the activity and selectivity towards CO formation dramatically in CO 2 RR, whereas the turnover and selectivity drop to a level similar to Ag foil when the ligand layer was removed (Fig. 24B and C), supporting the importance of the NOLI structure in the selective CO 2 -to-CO transformation.…”
Given the continuous and excessive CO2 emission into the atmosphere from anthropomorphic activities, there is now a growing demand for negative carbon emission technologies, which requires efficient capture and conversion...
“…Specifically, the ligand chains form a hydrophobic domain around the pocket that facilitates the diffusion of CO 2 , while inhibiting the diffusion of water/protons, into the NOLI structure, favouring CO 2 conversion over the HER. 192 The Ag–NOLI improved the activity and selectivity towards CO formation dramatically in CO 2 RR, whereas the turnover and selectivity drop to a level similar to Ag foil when the ligand layer was removed (Fig. 24B and C), supporting the importance of the NOLI structure in the selective CO 2 -to-CO transformation.…”
Given the continuous and excessive CO2 emission into the atmosphere from anthropomorphic activities, there is now a growing demand for negative carbon emission technologies, which requires efficient capture and conversion...
“…[23][24][25] Among these approaches, the incorporation of rationally designed surface ligands on nanocatalysts has attracted much attention recently. [26][27][28][29][30][31][32][33][34][35] As inspired by metalloenzymes where the stability and overall efficiency of the active metal sites rely on nely engineered protein frameworks, passive organic ligands anchored to the surface of nanocatalysts can stabilize nanocatalysts and simultaneously provide a similar microenvironment that controls the selectivity for CO 2 electroreduction. 27,36 Ligands at the catalyst-electrolyte interface where the reduction normally occurs control how substrates bind/activate on the catalyst and/or stabilize key rection intermediates, simultaneously preventing the interparticle coalescence.…”
We report the use of polymer N-heterocyclic carbenes (NHCs) to control the microenvironment surrounding metal nanocatalysts, thereby enhancing their catalytic performance in CO2 electroreduction. Three polymer NHC ligands were...
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