Molten-salt-assisted synthesis of single-atom iron confined N-doped carbon nanosheets for highly efficient industrial-level CO2 electroreduction and Zn-CO2 batteries
“…402.1 and 404.6 eV attributed to the graphite N and oxidized N, respectively. 29,32,37,39,50–54 Compared with Fe–poN 4 –C (400.8 eV), the binding energy peak position of pyrrole N in S/Fe–poN 4 –C (400.9 eV) shifted upward, while the peak position of pyridine N (398.2 eV) in S/Fe–poN 4 –C and Fe–poN 4 –C did not shift. Similar results to S/Fe–poN 4 –C could be obtained for the S/Fe–pdN 4 –C catalysts.…”
Section: Resultsmentioning
confidence: 93%
“…The energy barrier to form *COOH was significantly lower for S-doped catalysts S/Fe–pdN 4 –C and S/Fe–poN 4 –C compared to that for S-undoped counterparts Fe–pdN 4 –C and Fe–poN 4 –C, confirming that S and Fe–N 4 can induce p–d orbital interactions to enhance the binding strength of the *COOH intermediate toward the surface of the catalysts. 65,66 It is known that weak adsorption of the *CO intermediate favors the generation of CO. 3,51 The desorption energy of the *CO intermediate was −0.61 eV (Fe–pdN 4 –C), −0.38 eV (S/Fe–pdN 4 –C), −0.11 eV (Fe–poN 4 –C), and −0.19 eV (S/Fe–poN 4 –C), respectively. The formation of CO in Fe–pdN 4 –C and S/Fe–pdN 4 –C was prevented by the high desorption energy of the *CO intermediate.…”
Electrochemical CO2 reduction reaction (CO2RR) to CO is closely correlated with appropriate sorption of *COOH and *CO species toward the electrode surface, and the proton transfer process that often competes...
“…402.1 and 404.6 eV attributed to the graphite N and oxidized N, respectively. 29,32,37,39,50–54 Compared with Fe–poN 4 –C (400.8 eV), the binding energy peak position of pyrrole N in S/Fe–poN 4 –C (400.9 eV) shifted upward, while the peak position of pyridine N (398.2 eV) in S/Fe–poN 4 –C and Fe–poN 4 –C did not shift. Similar results to S/Fe–poN 4 –C could be obtained for the S/Fe–pdN 4 –C catalysts.…”
Section: Resultsmentioning
confidence: 93%
“…The energy barrier to form *COOH was significantly lower for S-doped catalysts S/Fe–pdN 4 –C and S/Fe–poN 4 –C compared to that for S-undoped counterparts Fe–pdN 4 –C and Fe–poN 4 –C, confirming that S and Fe–N 4 can induce p–d orbital interactions to enhance the binding strength of the *COOH intermediate toward the surface of the catalysts. 65,66 It is known that weak adsorption of the *CO intermediate favors the generation of CO. 3,51 The desorption energy of the *CO intermediate was −0.61 eV (Fe–pdN 4 –C), −0.38 eV (S/Fe–pdN 4 –C), −0.11 eV (Fe–poN 4 –C), and −0.19 eV (S/Fe–poN 4 –C), respectively. The formation of CO in Fe–pdN 4 –C and S/Fe–pdN 4 –C was prevented by the high desorption energy of the *CO intermediate.…”
Electrochemical CO2 reduction reaction (CO2RR) to CO is closely correlated with appropriate sorption of *COOH and *CO species toward the electrode surface, and the proton transfer process that often competes...
“…Methanol (CH 3 OH) and methane (CH 4 ) can be produced during the reduction of H protons. 112 It is particularly important to note that HCHO and CH 3 OH are two intermediates rather than reaction by-products, and the C–O cleavage reaction is always accompanied by a protonation reaction. However, the production of CO is unable to be revealed by the formaldehyde pathway.…”
Section: Application Of Dascs In Photocatalytic Conversion Of Small M...mentioning
Herein, the recent progress of DASCs in the field of photocatalytic conversion of small molecules is reviewed, including controllable preparation and characterization, reaction mechanisms and the relationship between their structure and activity.
“…For example, in 2022, Yang et al. 75 successfully prepared 2D N-doped carbon NSs loaded with Fe single-atom catalysts by the molten salt process. The advantage of the molten salt process over the previously mentioned synthesis methods is the high synthetic efficiency.…”
Section: Strategy For the Synthesis Of Cu-based 2d Materialsmentioning
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