Preparation and Properties of Proton Conductors and HER Electrocatalysts Based on Multifunctional Transition Metal Sulfophosphonates.

dc.centroFacultad de Cienciases_ES
dc.contributor.authorVílchez-Cózar, Álvaro
dc.contributor.authorSalcedo, Inés R.
dc.contributor.authorXanthopoulos, Konstantinos
dc.contributor.authorPérez-Colodrero, Rosario Mercedes
dc.contributor.authorBazaga-García, Montse
dc.contributor.authorDemadis, Konstantinos D.
dc.contributor.authorOlivera-Pastor, Pascual
dc.contributor.authorCabeza-Díaz, Aurelio
dc.date.accessioned2025-09-22T11:18:00Z
dc.date.available2025-09-22T11:18:00Z
dc.date.issued2025
dc.departamentoQuímica Inorgánica, Cristalografía y Mineralografíaes_ES
dc.description.abstractPreparation and Properties of Proton Conductors and HER Electrocatalysts Based on Multifunctional Transition Metal Sulfophosphonates Transition metal phosphonates are multifunctional materials with potential applications in energy storage and conversion technologies [1]. These materials exhibit proton-conducting properties and are attractive precursors for the preparation of electrocatalysts [2,3]. Thus, their structurally tunable properties facilitate, on one hand, the formation of efficient proton transport pathways, and on the other, their pyrolytic conversion into electrocatalytically active transition metal phosphides or polyphosphates [4]. Herein, we report the synthesis, structural diversity, and electrochemical characterization of a series of transition metal sulfophosphonates (M = Mn2+, Fe2+, Co2+, Zn2+) derived from 2-[bis(phosphonomethyl)amino]ethanesulfonic acid (SPA). Their crystal structures were determined using synchrotron and laboratory X-ray powder diffraction, allowing structure–property correlations to be established. Depending on the material composition, the proton conductivity values ranged from 10-4 S·cm-1 (Mn2+, Fe2+, and Co2+ derivatives) to 10-2 S·cm-1 (mixed NH4+/Zn2+ derivative) at 80°C and 95% relative humidity, with all compounds exhibiting a water-mediated proton transfer mechanism. In addition, among the transition metal materials pyrolyzed under (5%)H2–Ar atmosphere, the Co-based derivative treated at 700°C, consisting of mixed o-CoP and o-Co2P phases, exhibited the best performance in the hydrogen evolution reaction (HER), achieving overpotentials of only 91 and 95 mV at 10 mA·cm-2 under acidic and alkaline conditions, respectively, when supported on a CFP substrate.es_ES
dc.description.abstractReferences [1] P. Bhanja, J. Na, T. Jing, J. Lin, T. Wakihara, A. Bhaumik, Y. Yamauchi. Chem. Mater. 31 (2019), 5343–5362. [2] S.-S. Bao, G.K.H. Shimizu, L.-M. Zheng. Coord. Chem. Rev. 378 (2019), 577–594. [3] R. Zhang, S.M. El-Refaei, P.A. Russo, N. Pinna. J. Nanopart. Res. 20 (2018), 146. [4] Á. Vílchez-Cózar, R. M. P. Colodrero, M. Bazaga-García, D. Marrero-López, S. M. El-Refaei, P. A. Russo, N. Pinna, P. Olivera-Pastor, A. Cabeza. Appl. Catal. B 337 (2023), 122963.es_ES
dc.identifier.urihttps://hdl.handle.net/10630/39989
dc.language.isoenges_ES
dc.relation.eventdate17 al 19 de Septiembre de 2025es_ES
dc.relation.eventplacePerugia (Italia)es_ES
dc.relation.eventtitle5th International Conference on Phosphonate Chemistry, Science, and Technology (ICOPHOS-5)es_ES
dc.relation.projectIDPID2019-110249RB-I00es_ES
dc.relation.projectIDTED2021-129836B-I00es_ES
dc.relation.projectIDPID2023-148883OB-I00es_ES
dc.relation.projectIDB1-2023_006 (UMA)es_ES
dc.relation.projectIDPRE2020-094459es_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectRayos X - Difracciónes_ES
dc.subjectEstructura cristalina (Sólidos)es_ES
dc.subjectSincrotroneses_ES
dc.subjectCatalizadores de metales de transiciónes_ES
dc.subject.otherX ray diffractiones_ES
dc.subject.otherMetal phosphonateses_ES
dc.subject.otherProton conductivityes_ES
dc.subject.otherSynchrotrones_ES
dc.subject.otherElectrocatalystses_ES
dc.subject.otherMetal phosphideses_ES
dc.subject.otherCrystal structurees_ES
dc.titlePreparation and Properties of Proton Conductors and HER Electrocatalysts Based on Multifunctional Transition Metal Sulfophosphonates.es_ES
dc.typeconference outputes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication1fb49d6b-6f8a-4357-be3e-1e04b79508b9
relation.isAuthorOfPublication3ffbfa2c-440f-43d4-a365-5da9871e63ba
relation.isAuthorOfPublication8f4b8f61-7f72-4549-a437-4610bca45855
relation.isAuthorOfPublication.latestForDiscovery1fb49d6b-6f8a-4357-be3e-1e04b79508b9

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