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Details

Autor(en) / Beteiligte
Titel
Hydrothermally/electrochemically decorated FeSe on Ni-foam electrode: An efficient bifunctional electrocatalysts for overall water splitting in an alkaline medium
Ist Teil von
  • International journal of hydrogen energy, 2020-10, Vol.45 (51), p.27182-27192
Ort / Verlag
Elsevier Ltd
Erscheinungsjahr
2020
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • A new hybrid catalyst based on Ni foam (NF) and FeSe was prepared by a facial hydrothermal method, in which Se-decorated NF was subsequently electrochemically doped by Fe. Binder-free catalyst containing electrodes were directly tested for the hydrogen and oxygen evolution reaction (HER/OER). The FeSe/NF electrode displayed an OER current density of 100 mA cm−2 at potential of 1.42 V, and a relatively small Tafel slope of 109 mV dec−1 in a 1 M KOH solution. Also, FeSe/NF electrode exhibited reasonable HER overpotential of 200 mV at 10 mAcm−2 current density with Tafel slope of 145 mV dec−1. The XRD and TEM studies revealed that the formation of heterogeneous interfaces of NiSe2 and FeSe2,generated more active sites that can promote better ions and electron transport in the electrode/electrolyte interfaces. Furthermore, HRTEM analysis indicates that FeSe2 rich in Se vacancy defects can be created with suitable M − O and M − H bond for better OER and HER performance, respectively. In a-two electrode alkaline water electrolyzer, current densities of 10 mA cm−2 and 50 mA cm−2 were obtained at cell voltages of 1.52 V and 1.85 V, respectively, using pure FeSe–NF as both the cathode and anode. TOC: A binder free FeSe–Ni foam electrode is obtained, which shows remarkable bifunctional activity of overall water splitting. [Display omitted] •FeSe catalysts are synthesized on the Ni foam layer.•FeSe–Ni foam showed excellent bifunctional water splittting catalysts.•NiSe2 and FeSe2 heterointerfaces are formed.•FeSe–Ni foam is a stable and efficient catalyst.
Sprache
Englisch
Identifikatoren
ISSN: 0360-3199
eISSN: 1879-3487
DOI: 10.1016/j.ijhydene.2020.07.055
Titel-ID: cdi_crossref_primary_10_1016_j_ijhydene_2020_07_055

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