Abstract
Tandem catalysis, capable of decoupling individual steps, provides a feasible way to build a high-efficiency CO2 electroconversion system for multicarbons (C2+). The construction of electrocatalytic materials is one of focusing issues. Herein, we fabricated a single atom involved multivalent oxide-derived Cu composite material and found it inclined to reconstruct into oxygen-deficient multiphase Cu based species hybridized with monatomic Ni on N doped C matrix. In this prototype, rapid CO generation and C–C coupling are successively achieved on NiN4 sites and surface amorphized Cu species with defects, resembling a micro-production line. In this way, the in situ formed tandem catalyst exhibited a high Faradaic efficiency (FE) of ∼ 78% for C2+ products along with satisfactory durability over 50 h. Particularly, the reconstruction-induced amorphous layer with abundant asymmetric sites should be favorable to improve the ethanol selectivity (FE: 63%), which is about 10 times higher than that of the non-tandem Cu-based contrast material. This work offers a new approach for manipulating tandem catalyst systems towards enhancing C2+ products.
| Original language | English |
|---|---|
| Pages (from-to) | 3888-3894 |
| Number of pages | 7 |
| Journal | Nano Research |
| Volume | 17 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - May 2024 |
| Externally published | Yes |
Keywords
- CO reduction reaction
- amorphous
- reconstruction
- single atom
- tandem catalysis
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