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Parameters Affecting the Fuel Cell Reactions on Platinum Bimetallic Nanostructures

Electrochemical Energy Reviews 2023年第1期6卷 830-853页

作者： Nicolas Alonso‑Vante IC2MP UMR-CNRS 7285University of Poitiers4 rue Michel Brunet86072 PoitiersFrance

In this paper the electrochemical properties of some platinum-based nanoalloys are reviewed.The revision is centered on electrocatalytic materials generated via the carbonyl chemical route(CCR).In considering the effects of segregation in these bimetals,the reaction of the hydrogen oxidation(HOR)and oxygen reduction(ORR)in the alkaline medium was investigated.The reaction kinetics of these electrochemical processes in the alkaline electrolyte is still a challenge.For the design of high-performance platinum-based electrocatalysts,it is of importance to know that the kinetics of HOR and ORR also depends on the Pt adsorbate.The electrochemical analysis,based on the study of Pt nanoalloyed surfaces with different Pt-adsorbate interactions,was taken into account.A clear trend in the HOR as well as the ORR activity,in the alkaline electrolyte,was established,revealing that the activity changes in the order PtSn/C

关键词： Electrocatalysts HOR HER ORR Pt-based materials Bimetallic Carbon domains

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Bifunctional oxygen electrode cobalt–nickel sulfides catalysts originated from intercalated LDH precursors

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Journal of Energy Chemistry 2022年第11期31卷 376-386,I0010页

作者： Xiaofei Gong Haihong Zhong Luis Alberto Estudillo-Wong nicolas alonso-vante Yongjun Feng Dianqing Li State Key Laboratory of Chemical Resource Engineering Beijing Engineering Center for Hierarchical CatalystsCollege of ChemistryBeijing University of Chemical TechnologyBeijing 100029China Departamento de Sociedad y Política Ambiental CIIEMADInstituto Politécnico NacionalCalle 30 de junio de 1520Alcaldía GAMC.P.07340 CDMXMexico IC2MP UMR-CNRS 7285University of PoitiersF-86073 Poitiers CedexFrance

Bimetallic cobalt-nickel sulfide nanoparticles anchored on S-,N-codoped holey carbon nanosheets(CoNiS-T@NCFs)with a hydrangea-like morphology,were synthesized via a confinement synthesis route,in which an intercalated LDH precursor was subjected to the interlayer-confined carbonization and host-layer sulfurization.The phase transformation and structure evolution(e.g.,atom site occupancy,crystallite size,and cell volume)of the CoNi-S-T@NCFs electrocatalysts,as a function of sulfurization temperatures,were confirmed by X-ray diffraction and Rietveld analyses.The sulfur vacancies effectively enhance the electrocatalytic activity,while the synergistic effect of(Co,Ni)7 S8 alloy and S,N-codoped carbon matrix facilitates the electron transfer and accelerates reaction kinetics,making CoNi-S-900@NCFs an efficient and stable bifunctional electrocatalyst for oxygen reduction reaction(ORR).The rich highvalence Co(Ⅲ)and Ni(Ⅲ)of CoNi-S-900@NCFs facilitates the in-situ transformation of the metal(oxy)hydroxides intermediates with high catalytic activity for oxygen evolution reaction(OER).Thus,with a bifunctional parameter,ΔE,of 0.75 V(E_(j=10,OER)-E_(1/2,ORR)),this electrocatalyst slightly outperforms the state-of-the-art commercial Pt/C+RuO_(2)/C catalyst(ΔE=0.76 V)in alkaline medium.This work demonstrates the influence that the sulfurization temperature has on the relationship between the structure and electrocatalytic performance of bimetallic sulfides prepared by the synthesis strategy using the intercalated LDH precursor.This strategy can be extended to prepare other chalcogenides with binary or ternary transition metals.

关键词： Bimetallic sulfides Confinement synthesis LDHs ORR OER

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Oxygen vacancies engineering by coordinating oxygen-buffering CeO_(2) with CoO_(x) nanorods as efficient bifunctional oxygen electrode electrocatalyst

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Journal of Energy Chemistry 2021年第8期30卷 615-625,I0013页

作者： Haihong Zhong Luis Alberto Estudillo-Wong Yuan Gao Yongjun Feng nicolas alonso-vante State Key Laboratory of Chemical Resource Engineering Beijing Engineering Center for Hierarchical CatalystsCollege of ChemistryBeijing University of Chemical TechnologyNo.15 Beisanhuan East Road100029 BeijingChina IC2MP UMR-CNRS 7285University of PoitiersF-86022 Poitiers CedexFrance Departamento de Sociedad y Política Ambiental CIIEMADInstituto Politécnico NacionalCalle 30 de junio de 1520Alcaldía GAMC.P.07340 CDMXMexico Anqing Research Institute Beijing University of Chemical TechnologyNo.8 Huanhu West RoadHigh-Tech DistrictAnqing 24600China

CeO_(2)decorated CoOx rod-like hybrid,supported onto holey reduced graphene(CoOx/CeO_(2)/RGO)composite,was fabricated via a surfactant-assisted route.Its corresponding electrocatalytic performance towards oxygen reduction/evolution reactions(ORR and OER)was systematically investigated in alkaline electrolyte.Structural,morphological and compositional studies revealed changes in electronic and surface properties when CeO_(2)was introduced as an oxygen buffer material.The oxygen vacancies effectively enhanced the electrocatalytic activity,while the synergistic effect of co-catalyst CeO_(2),CoOx activecenters,and defective graphene with many voids facilitate the charge/mass transfer,making CoOx/CeO_(2)/RGO an efficient and stable bifunctional electrocatalyst for OER/ORR with△E=0.76 V(△E=E10mAcm.-2OER-E_(1/2).ORR).This parameter is 70 mV and 270 mV lower than CoOx/RGO and the benchmark Pt/C,respectively.In addition,the OER/ORR bifunctionality of CoOx/CeO_(2)/RGO composite outperforms that of Pt/C catalyst in a H2-O_(2)micro fuel cell platform.

关键词： Co3O4 CeO_(2) Oxygen vacancies ORR OER

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