Coordination tailoring of Cu single sites on C3N4 realizes selective CO2 hydrogenation at low temperature
CO 2 hydrogenation has attracted great attention, yet the quest for highly-efficient catalysts is driven by the current disadvantages of poor activity, low selectivity, and ambiguous structure-performance relationship. We demonstrate here that C 3 N 4 -supported Cu single atom catalysts with tailore...
Uložené v:
| Vydané v: | Nature communications Ročník 12; číslo 1; s. 6022 - 9 |
|---|---|
| Hlavní autori: | , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
London
Nature Publishing Group UK
15.10.2021
Nature Publishing Group Nature Portfolio |
| Predmet: | |
| ISSN: | 2041-1723, 2041-1723 |
| On-line prístup: | Získať plný text |
| Tagy: |
Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
|
| Shrnutí: | CO
2
hydrogenation has attracted great attention, yet the quest for highly-efficient catalysts is driven by the current disadvantages of poor activity, low selectivity, and ambiguous structure-performance relationship. We demonstrate here that C
3
N
4
-supported Cu single atom catalysts with tailored coordination structures, namely, Cu–N
4
and Cu–N
3
, can serve as highly selective and active catalysts for CO
2
hydrogenation at low temperature. The modulation of the coordination structure of Cu single atom is readily realized by simply altering the treatment parameters. Further investigations reveal that Cu–N
4
favors CO
2
hydrogenation to form CH
3
OH via the formate pathway, while Cu–N
3
tends to catalyze CO
2
hydrogenation to produce CO via the reverse water-gas-shift (RWGS) pathway. Significantly, the CH
3
OH productivity and selectivity reach 4.2 mmol g
–1
h
–1
and 95.5%, respectively, for Cu–N
4
single atom catalyst. We anticipate this work will promote the fundamental researches on the structure-performance relationship of catalysts.
CO
2
hydrogenation has attracted intense scientific attention yet suffers from the disadvantage of poor activity and low selectivity. Here, the authors report that Cu single atom catalysts with tailored coordination environments on C
3
N
4
serve as highly selective catalysts for CO
2
hydrogenation. |
|---|---|
| Bibliografia: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| ISSN: | 2041-1723 2041-1723 |
| DOI: | 10.1038/s41467-021-26316-6 |