Accelerating charge transfer at an ultrafine NiFe-LDHs/CB interface during the electrocatalyst activation process for water oxidation. Issue 22 (20th May 2020)

• Record Type: Journal Article
• Authors: Cai, Mengke; Liu, Qinglin; Zhao, Yiyue; Wang, Zhenyu; Li, Yinle; Li, Guangqin
• Is Part Of: Dalton transactions. Volume 49:Issue 22(2020)
• Page Start: 7436
• Page End: 7443
• Publication Date: 2020-05-20
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d0dt00824a
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Benefiting from chemical bonding interface and homogeneity of active sites, NiFe-LDHs/CB possesses a faster nickel redox process, a tighter interface structure, and an increased number of active sites during activation process. Abstract : Owing to the combination of intriguing activity and conductivity, hybrid compositions of layered double hydroxides (LDHs) and carbon-based materials have been extensively and widely applied to evolve oxygen gas during water splitting. Here, a facile in situ nucleation strategy was used to construct ultrafine NiFe-LDH nanosheets monodispersed on a carbon black (CB) substrate. Notably, this work displayed the interfacial impact of combining CB with NiFe-LDHs on electrocatalyst activation. Interestingly, the optimized NiFe-LDHs/CB composite displays a fast activation rate and excellent water oxidation performance on a glassy-carbon electrode (an overpotential of 226 mV at 10 mA cm −2 ; a Tafel slope of 57 mV dec −1 ). This is due to the high active area, low impedance and ultra-high active metal atom utilization rate, accelerating charge transfer at the interface during the activation process. More importantly, this work highlights the interfacial charge transfer effect during the activation process and supplies clues for designing electrocatalysts.