TY - JOUR
T1 - Facile electrochemical preparation of NiFeP submicron-spheres as an efficient electrocatalyst for the electrochemical hydrogenation of 4-nitrophenol at neutral pH
AU - Huang, Shih Ching
AU - You, Zheng Xun
AU - Jhang, Shun Min
AU - Lin, Chia Yu
N1 - Funding Information:
Financial support from the National Science and Technology Council of Taiwan ( 110-2221-E-006-018-MY3 and 111-2221-E-006-019-MY3 ). This work was also financially supported by the Hierarchical Green-Energy Materials (Hi-GEM) Research Center, from The Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education ( MOE ) and the National Science and Technology Council ( 111-2634-F-006-008 ) in Taiwan. The authors would also like to thank the use of ESCA003200 and XRD005100 belonging to the Core Facility Center of National Cheng Kung University .The authors gratefully acknowledge the use of ESCA003200 and XRD005100 of NSTC 110-2731-M-006-001 belonging to the Core Facility Center of National Cheng Kung University.
Publisher Copyright:
© 2022 Elsevier Ltd.
PY - 2022/12
Y1 - 2022/12
N2 - Electrochemical hydrogenation with water as the proton source serves as a clean and sustainable alternative to the removal and upcycling of 4-nitrophenol (4-NP), one of the major toxic pollutants commonly present in industrial wastewater effluents, into value-added chemicals (e.g., 4-aminophenol), but the development of high-performance electrocatalyst for electrochemical hydrogenation of 4-NP (e-NPR) at neutral pH remains challenging. Herein, we represent the facile electrochemical synthesis of micro-structured nickel-iron phosphide (microNiFeP), which acts as an efficient electrocatalyst in catalyzing hydrogen evolution reaction (HER) and e-NPR at neutral pH. The effects of electrosynthetic conditions on the physicochemical and electrocatalytic properties of microNiFeP were investigated and optimized. microNiFeP, prepared with optimized conditions, consisted of submicron-sized spheres (diameter: ∼200 nm) with wrinkled surface and exhibited promising HER activity, reaching a turnover frequency (TOF) of 47.18 ± 4.10 h-1 at - 0.2 V vs. reversible hydrogen electrode (RHE) at pH 7 in the absence of 4-NP. In the presence of 4-NP, however, microNiFeP exhibited high e-NPR activity and selectivity against HER. Notably, microNiFeP showed a TOF of 5.12 ± 0.48 h-1 for e-NPR at 0.0 V vs. RHE and enabled conversion of 89.6 ± 3.3 % with a Faradic efficiency of 81.98 ± 5.08 % for 4-aminophenol production after 8-h-controlled-potential electrolysis at - 0.2 V vs. RHE. Mechanistic studies reveal that e-NPR at microNiFeP involved the transfer of 5.3 ∼5.8 electrons and may involve the formation of 4,4'-dihydroxyazobenzene as one of the side products.
AB - Electrochemical hydrogenation with water as the proton source serves as a clean and sustainable alternative to the removal and upcycling of 4-nitrophenol (4-NP), one of the major toxic pollutants commonly present in industrial wastewater effluents, into value-added chemicals (e.g., 4-aminophenol), but the development of high-performance electrocatalyst for electrochemical hydrogenation of 4-NP (e-NPR) at neutral pH remains challenging. Herein, we represent the facile electrochemical synthesis of micro-structured nickel-iron phosphide (microNiFeP), which acts as an efficient electrocatalyst in catalyzing hydrogen evolution reaction (HER) and e-NPR at neutral pH. The effects of electrosynthetic conditions on the physicochemical and electrocatalytic properties of microNiFeP were investigated and optimized. microNiFeP, prepared with optimized conditions, consisted of submicron-sized spheres (diameter: ∼200 nm) with wrinkled surface and exhibited promising HER activity, reaching a turnover frequency (TOF) of 47.18 ± 4.10 h-1 at - 0.2 V vs. reversible hydrogen electrode (RHE) at pH 7 in the absence of 4-NP. In the presence of 4-NP, however, microNiFeP exhibited high e-NPR activity and selectivity against HER. Notably, microNiFeP showed a TOF of 5.12 ± 0.48 h-1 for e-NPR at 0.0 V vs. RHE and enabled conversion of 89.6 ± 3.3 % with a Faradic efficiency of 81.98 ± 5.08 % for 4-aminophenol production after 8-h-controlled-potential electrolysis at - 0.2 V vs. RHE. Mechanistic studies reveal that e-NPR at microNiFeP involved the transfer of 5.3 ∼5.8 electrons and may involve the formation of 4,4'-dihydroxyazobenzene as one of the side products.
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U2 - 10.1016/j.jece.2022.108882
DO - 10.1016/j.jece.2022.108882
M3 - Article
AN - SCOPUS:85141935812
SN - 2213-3437
VL - 10
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
IS - 6
M1 - 108882
ER -