Source abstract
Abstract
Carbon black (CB) has been well-documented as an effective catalyst support for enhancing the performance and cost-effectiveness of catalysts in various electrochemical reactions. However, studies of these materials as catalyst supports for the CO 2 reduction reaction are still limited. Therefore, in this study, we developed a simple approach involving the modification of supporting carbon black nanoparticles (∼29 nm) to improve the activity and stability of the SnO 2 catalyst under industrially relevant conditions. Carbon black, as the supporting material, underwent calcination at moderate temperatures (350–550 °C) in the atmosphere, and the effects of the thermal treatment on the catalytic performance of the commercial SnO 2 catalyst were examined. Electrochemical measurements revealed that SnO 2 supported on CB thermally treated at 450 °C (SnO 2 /CB-450) exhibited superior activity and stability at industrially relevant current densities compared with other samples. While the SnO 2 -only and nontreated CB-supported samples showed rapid performance decay, the SnO 2 /CB-450 electrode maintained a Faradaic efficiency above 80% after 4 h and above 70% after 12 h of electrolysis in 2 M KOH at 200 mA cm –2 . The impacts of the thermally treated CB on the electrocatalytic performance of SnO 2 were assessed using various morphological and structural analyses, revealing a thermal treatment-induced surface modification of the CB nanomaterial support that effectively enhanced electrical conductivity and promoted the interaction and charge transfer between the catalyst and support, thereby improving overall catalyst performance and stability. Despite improvements, stability remains challenging, and the chemical and morphological changes of the electrode during the reaction were investigated over time to better understand the issue. This work introduces a straightforward and scalable strategy to enhance the activity and stability of the SnO 2 catalyst by modifying the carbon black nanomaterial support, offering a practical and scalable implication for the electrochemical CO 2 reduction reaction at high current densities.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Biochemistry, Chemistry, Physics and Forensic Science, Université du Québec à Trois-Rivières (UQTR), 3351 Boulevard des Forges, Trois-Rivières, Québec G8Z 4M3, Canada
Laboratory of Advanced Materials for Energy and Environment (Nguyen-Tri Lab), Université du Québec à Trois-Rivières (UQTR), 3351 Bd. des Forges, Trois-Rivières, QC G8Z 4M3, Canada
Electro Carbon, Inc., Local #261, 3275 Chemin de l’Industrie, St-Mathieu-de-Beloeil, QC J3G 0M8, Canada
Department of Chemical Engineering, Polytechnique Montréal, C.P. 6079, Succ. CV, Montréal, Québec H3C 3A7, Canada
Funding
Natural Sciences and Engineering Research Council of Canada · Mitacs · Electro Carbon Inc.