TY - JOUR
T1 - Deep reconstruction of Ni-Al-based pre-catalysts for a highly efficient and durable anion-exchange membrane (AEM) electrolyzer
AU - Jiang, Tao
AU - Jiang, Xinge
AU - Kyriakou, Vasileios
AU - Bouzek, Karel
AU - Liao, Hanlin
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/12/21
Y1 - 2023/12/21
N2 - The anion exchange membrane (AEM) electrolyzer has shown great potential for producing green hydrogen. However, this technology is still in its early stages and has not yet been applied on an industrial scale. One of the most significant challenges is the lack of cost-effective and scalable techniques for producing highly active, durable, and earth-abundant metal-based catalysts. Herein, we present a scalable thermal spraying process for fabricating defect-rich nickel-based HNA-CA that can function as an efficient pre-catalyst for both (hydrogen evolution reaction) HER and (oxygen evolution reaction) OER. Particularly, after deep reconstruction through simple electrochemical activation, the obtained HNA-CA-H and HNA-CA-O exhibit the lowest overpotential of −31 mV (HER) and 188 mV (OER) at 10 mA cm−2, surpassing that of noble metal-based catalysts such as Pt and IrO2, respectively. By coupling two 5 cm2 electrodes, the resulting HNA-CA-H(-)‖HNA-CA-O(+) AEM electrolyzer cell demonstrates exceptional performance, achieving an extraordinarily low cell voltage of 1.89 V at 1 A cm−2 (1 M KOH, room temperature). Furthermore, it showcases remarkable durability, sustaining operation for an impressive 500 hours at 5 A (1 A cm−2). These performance metrics notably outclass the majority of AEM electrolyzers reported under comparable operational settings. The outcomes can primarily be ascribed to the substantial improvements in interfacial contact, charge transfer efficiency, and mass transport mechanisms, all of which were comprehensively unveiled through in situ impedance analysis, ex situ structural characterization, and a thorough investigation of wettability and bubble dynamics. These findings hold significant promise for expediting the advancement and practical deployment of AEM electrolysis technology.
AB - The anion exchange membrane (AEM) electrolyzer has shown great potential for producing green hydrogen. However, this technology is still in its early stages and has not yet been applied on an industrial scale. One of the most significant challenges is the lack of cost-effective and scalable techniques for producing highly active, durable, and earth-abundant metal-based catalysts. Herein, we present a scalable thermal spraying process for fabricating defect-rich nickel-based HNA-CA that can function as an efficient pre-catalyst for both (hydrogen evolution reaction) HER and (oxygen evolution reaction) OER. Particularly, after deep reconstruction through simple electrochemical activation, the obtained HNA-CA-H and HNA-CA-O exhibit the lowest overpotential of −31 mV (HER) and 188 mV (OER) at 10 mA cm−2, surpassing that of noble metal-based catalysts such as Pt and IrO2, respectively. By coupling two 5 cm2 electrodes, the resulting HNA-CA-H(-)‖HNA-CA-O(+) AEM electrolyzer cell demonstrates exceptional performance, achieving an extraordinarily low cell voltage of 1.89 V at 1 A cm−2 (1 M KOH, room temperature). Furthermore, it showcases remarkable durability, sustaining operation for an impressive 500 hours at 5 A (1 A cm−2). These performance metrics notably outclass the majority of AEM electrolyzers reported under comparable operational settings. The outcomes can primarily be ascribed to the substantial improvements in interfacial contact, charge transfer efficiency, and mass transport mechanisms, all of which were comprehensively unveiled through in situ impedance analysis, ex situ structural characterization, and a thorough investigation of wettability and bubble dynamics. These findings hold significant promise for expediting the advancement and practical deployment of AEM electrolysis technology.
UR - http://www.scopus.com/inward/record.url?scp=85178280385&partnerID=8YFLogxK
U2 - 10.1039/d3ta05775e
DO - 10.1039/d3ta05775e
M3 - Article
AN - SCOPUS:85178280385
SN - 2050-7488
VL - 11
SP - 26011
EP - 26022
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 47
ER -