Molecular Catalyst Enables CO2Electroreduction at 650 mA/cm2CO Partial Current Density
ACS Energy Letters, cilt.10, ss.4957-4961, 2025 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 10
- Basım Tarihi: 2025
- Doi Numarası: 10.1021/acsenergylett.5c02397
- Dergi Adı: ACS Energy Letters
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Compendex, INSPEC
- Sayfa Sayıları: ss.4957-4961
- Marmara Üniversitesi Adresli: Evet
Özet
The electrochemical reduction of CO2to CO using renewable electricity offers a compelling pathway for greenhouse gas recycling. The two-electron, two-proton process is particularly attractive due to its operational simplicity and scalability, with copper- and silver-based nanomaterials being the most widely studied catalysts as the field approaches industrial maturity. However, achieving the necessary efficiency and stability for practical applications remains a significant challenge. Recently, molecular catalysts immobilized on conductive surfaces with carbon-based inks have emerged as highly tunable hybrid systems capable of remarkable selectivity. In this work, we report that a straightforward cobalt phthalocyanine complex, simply modified with a single trimethylammonium group, delivers outstanding CO2-to-CO conversion rates and selectivity, reaching a Faradaic efficiency of 93% at a total current density of 700 mA/cm2(jCO= 650 mA/cm2) at neutral pH. Notably, CO selectivity above 90% was sustained for over 42 h at 150 mA/cm2, illustrating the potential of simply designed molecular catalysts for large-scale applications.