دورية أكاديمية

Carbon dioxide and nitrate co-electroreduction to urea on CuO x ZnO y

التفاصيل البيبلوغرافية
العنوان: Carbon dioxide and nitrate co-electroreduction to urea on CuO x ZnO y
المؤلفون: Dimitra Anastasiadou, Bianca Ligt, Yunyang He, Rim C. J. van de Poll, Jérôme F. M. Simons, Marta Costa Figueiredo
المصدر: Communications Chemistry, Vol 6, Iss 1, Pp 1-8 (2023)
بيانات النشر: Nature Portfolio, 2023.
سنة النشر: 2023
المجموعة: LCC:Chemistry
مصطلحات موضوعية: Chemistry, QD1-999
الوصف: Abstract Urea is a commonly used nitrogen fertiliser synthesised from ammonia and carbon dioxide using thermal catalysis. This process results in high carbon dioxide emissions associated with the required amounts of ammonia. Electrocatalysis provides an alternative method to urea production with reduced carbon emissions while utilising waste products like nitrate. This manuscript reports on urea synthesis from the electroreduction of nitrate and carbon dioxide using CuOxZnOy electrodes under mild conditions. Catalysts with different ratios of CuO and ZnO, synthesised via flame spray pyrolysis, were explored for the reaction. The results revealed that all the CuOxZnOy electrocatalyst compositions produce urea, but the efficiency strongly depends on the metal ratio composition of the catalysts. The CuO50ZnO50 composition had the best performance in terms of selectivity (41% at −0.8 V vs RHE) and activity (0.27 mA/cm2 at −0.8 V vs RHE) towards urea production. Thus, this material is one of the most efficient electrocatalysts for urea production reported so far. This study systematically evaluates bimetallic catalysts with varying compositions for urea synthesis from carbon dioxide and nitrate.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2399-3669
Relation: https://doaj.org/toc/2399-3669
DOI: 10.1038/s42004-023-01001-5
URL الوصول: https://doaj.org/article/d875437dee71494e9c3528d9079a38a1
رقم الأكسشن: edsdoj.875437dee71494e9c3528d9079a38a1
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23993669
DOI:10.1038/s42004-023-01001-5