Wireless pulsed nanophotoelectrochemical cell for the ultrafast degradation of organic pollutants

An urgent demand exists for advanced-technologies to efficiently remove persistent organic pollutants from water, while minimizing energy consumption. Here, we introduce an innovative wireless nanophotoelectrochemical (nPEC) cell using pulsed light for the ultrafast degradation/mineralization of org...

Descripción completa

Detalles Bibliográficos
Autores: Serrà i Ramos, Albert, Gómez, Elvira, Al Hoda al Bast, Nour, Zhang, Yue, Duque, Marcos, Esplandiu, María J., Esteve, Jaume, Nogués, Josep, Sepúlveda, Borja
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/216276
Acceso en línea:https://hdl.handle.net/2445/216276
Access Level:acceso abierto
Palabra clave:Depuració de l'aigua
Antibiòtics
Nanotecnologia
Water purification
Antibiotics
Nanotechnology
Descripción
Sumario:An urgent demand exists for advanced-technologies to efficiently remove persistent organic pollutants from water, while minimizing energy consumption. Here, we introduce an innovative wireless nanophotoelectrochemical (nPEC) cell using pulsed light for the ultrafast degradation/mineralization of organic pollutants. The nPEC cell comprises a nanostructured Si-pn photodiode that monolithically integrates: (i) a Si-n/Au nanowire-based-photocathode for effective light absorption and photovoltage generation, and (ii) a Si-p/mesoporous-NiPt photoanode serving as catalyst to wirelessly amplify the sulfate radical production by low-intensity light without any bias voltage. The efficacy of the nPEC cell was shown by ultrafast degradation (>99 %) and mineralization (>98 %) of three emerging pollutants (tetracycline, levofloxacin and anatoxin-A). Notably, reaction kinetics were boosted by more than one order of magnitude when exposed to light intensities ca. 5-fold lower than sunlight. Remarkably, pulsed light beams in the 100–500 Hz range provided an additional enhancement in the degradation/mineralization efficiencies, reducing energy-input by half, while enhancing the catalyst's oxidation state and durability.