TY - JOUR
T1 - Nickel-based electrocatalysts for ammonia borane oxidation
T2 - enabling materials for carbon-free-fuel direct liquid alkaline fuel cell technology
AU - Zadick, Anicet
AU - Dubau, Laetitia
AU - Artyushkova, Kateryna
AU - Serov, Alexey
AU - Atanassov, Plamen
AU - Chatenet, Marian
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/7
Y1 - 2017/7
N2 - This paper introduces a new class of carbon-supported nickel-based electrocatalysts (Ni3Ag/C, Ni3Pd/C and Ni3Co/C) for the direct electrooxidation of ammonia borane (AB) in alkaline medium. The enabled anodic process opens the opportunity to build a novel concept of carbon-free-fuel energy conversion devices. Promising performances are reported for every studied catalyst. A trade-off is observed between the activity for the direct electrooxidation of AB and its decomposition (and related hydrogen release), as well as hydrogen oxidation reaction (HOR). The direct AB oxidation reaction (ABOR) onset is lower for the least noble materials (Ni3Co/C), due to its smaller catalytic activity for AB decomposition and hydrogen evolution, combined with a non-negligible activity for AB oxidation. On the contrary, on Ni3Pd/C, the noblest material, the onset of the ABOR is higher, because this material decomposes AB into hydrogen and evolves hydrogen, and then valorizes it. Moreover, Ni3Co/C exhibits a better durability than Ni3Ag/C, Ni3Pd/C, and than what is reported for Pt/C and Pd/C nanocatalysts in the literature in the same experimental conditions: identical-location transmission electron microscopy (ILTEM) investigations demonstrated no significant morphological degradations after accelerated stress tests (ASTs) in alkaline medium. This study therefore demonstrates that a carbon-supported nanostructured noble-free catalyst (Ni3Co/C) is both active and durable for the AB direct electrooxidation in alkaline medium. This result opens the way to direct liquid alkaline fuel cells fed with boron based fuels, a technology that could be both economically and industrially viable if noble-free catalysts are used.
AB - This paper introduces a new class of carbon-supported nickel-based electrocatalysts (Ni3Ag/C, Ni3Pd/C and Ni3Co/C) for the direct electrooxidation of ammonia borane (AB) in alkaline medium. The enabled anodic process opens the opportunity to build a novel concept of carbon-free-fuel energy conversion devices. Promising performances are reported for every studied catalyst. A trade-off is observed between the activity for the direct electrooxidation of AB and its decomposition (and related hydrogen release), as well as hydrogen oxidation reaction (HOR). The direct AB oxidation reaction (ABOR) onset is lower for the least noble materials (Ni3Co/C), due to its smaller catalytic activity for AB decomposition and hydrogen evolution, combined with a non-negligible activity for AB oxidation. On the contrary, on Ni3Pd/C, the noblest material, the onset of the ABOR is higher, because this material decomposes AB into hydrogen and evolves hydrogen, and then valorizes it. Moreover, Ni3Co/C exhibits a better durability than Ni3Ag/C, Ni3Pd/C, and than what is reported for Pt/C and Pd/C nanocatalysts in the literature in the same experimental conditions: identical-location transmission electron microscopy (ILTEM) investigations demonstrated no significant morphological degradations after accelerated stress tests (ASTs) in alkaline medium. This study therefore demonstrates that a carbon-supported nanostructured noble-free catalyst (Ni3Co/C) is both active and durable for the AB direct electrooxidation in alkaline medium. This result opens the way to direct liquid alkaline fuel cells fed with boron based fuels, a technology that could be both economically and industrially viable if noble-free catalysts are used.
KW - Activity
KW - Alkaline fuel cells
KW - Ammonia borane oxidation reaction (ABOR)
KW - Durability
KW - Identical-location transmission electron microscopy (ILTEM)
KW - Nickel
UR - http://www.scopus.com/inward/record.url?scp=85019364679&partnerID=8YFLogxK
U2 - 10.1016/j.nanoen.2017.05.035
DO - 10.1016/j.nanoen.2017.05.035
M3 - Article
AN - SCOPUS:85019364679
SN - 2211-2855
VL - 37
SP - 248
EP - 259
JO - Nano Energy
JF - Nano Energy
ER -