Details

Autor(en) / Beteiligte

• Kao, Bing‐Hsien
• Zeng, Yu‐Fang
• Lee, Yao‐Chang
• Pao, Chih‐Wen
• Chen, Jeng‐Lung
• Chuang, Yu‐Chun
• Sheu, Hwo‐Shuenn
• Tsai, Fu‐Te
• Liaw, Wen‐Feng

Titel

Unveiled the Structure‐Selectivity Relationship for Carbon Dioxide Reduction Triggered by Bi‐Doped Cu‐Based Nanocatalysts

Ist Teil von

• Small (Weinheim an der Bergstrasse, Germany), 2024-05, Vol.20 (20), p.e2307910-n/a

Ort / Verlag

Germany: Wiley Subscription Services, Inc

Erscheinungsjahr

2024

Quelle

Wiley Online Library

Beschreibungen/Notizen

• To investigate synergistic effect between geometric and electronic structures on directing CO2RR selectivity, water phase synthetic protocol and surface architecture engineering strategy are developed to construct monodispersed Bi‐doped Cu‐based nanocatalysts. The strongly correlated catalytic directionality and Bi3+ dopant can be rationalized by the regulation of [*COOH]/[*CO] adsorption capacities through the appropriate doping of Bi3+ electronic modulator, resulting in volcano relationship between FECO/TOFCO and surface EVBM values. Spectroscopic study reveals that the dual‐site binding mode ([Cu─μ─C(═O)O─Bi3+]) enabled by Cu1Bi3+2 motif in single‐phase Cu150Bi1 nanocatalyst drives CO2‐to‐CO conversion. In contrast, the study of dynamic Bi speciation and phase transformation in dual‐phase Cu50Bi1 nanocatalyst unveils that the Bi0‐Bi0 contribution emerges at the expense of BOC phase, suggesting metallic Bi0 phase acting as [H]˙ formation center switches CO2RR selectivity toward CO2‐to‐HCOO− conversion via [*OCHO] and [*OCHOK] intermediates. This work provides significant insight into how geometric architecture cooperates with electronic effect and catalytic motif/phase to guide the selectivity of electrocatalytic CO2 reduction through the distinct surface‐bound intermediates and presents molecular‐level understanding of catalytic mechanism for CO/HCOO− formation. This work provides significant insight into how geometric architecture (single‐phase vs dual‐phase) cooperates with electronic effect (surface d‐band center modulation by Bi3+ dopant) and catalytic motif/phase (Cu1Bi3+2 vs Bi0) to guide the selectivity of CO2 electro‐reduction through the distinct surface‐bound intermediates ([CO2]˙ˉ vs [H]˙) for CO/HCOO− formation.