Nanoparticle-Stacked Porous Nickel–Iron Nitride Nanosheet: A Highly Efficient Bifunctional Electrocatalyst for Overall Water Splitting

Wang, Yanyong; Xie, Chao; Liu, Dongdong; Huang, Xiaobing; Huo, Jia; Wang, Shuangyin

doi:10.1021/acsami.6b05811

Cited by 290 publications

(203 citation statements)

References 33 publications

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“…The peaks located at 532.5 eV and 531.4 eV were ascribed to the chemisorbed oxygen (O ads )a nd lattice oxygen (O lat ), respectively ( Figure 3c). For both NN and NIN, two different nitrogen speciesc an be observed from the N1ss pectra at 397.9 or 398.3 eV (N1), 399.3 (N2), which can be attributed to the metal nitride peak (i.e., À3N in NiÀN bonds) [37] and Co-N x structure, [44,45] respectively.I nterestingly,a negative shifto fN 1f rom 398.3 (NN) to 397.3 eV (NIN) can be distinguished (Figure 3d). For both NN and NIN, two different nitrogen speciesc an be observed from the N1ss pectra at 397.9 or 398.3 eV (N1), 399.3 (N2), which can be attributed to the metal nitride peak (i.e., À3N in NiÀN bonds) [37] and Co-N x structure, [44,45] respectively.I nterestingly,a negative shifto fN 1f rom 398.3 (NN) to 397.3 eV (NIN) can be distinguished (Figure 3d).…”

Section: Resultsmentioning

confidence: 99%

Phosphorus and Fluorine Co‐Doping Induced Enhancement of Oxygen Evolution Reaction in Bimetallic Nitride Nanorods Arrays: Ionic Liquid‐Driven and Mechanism Clarification

Bai

Wang

et al. 2017

Chemistry A European J

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Electrocatalytic splitting of water is becoming increasingly crucial for renewable energy and device technologies. As one of the most important half-reactions for water splitting reactions, the oxygen evolution reaction (OER) is a kinetically sluggish process that will greatly affect the energy conversion efficiency. Therefore, exploring a highly efficient and durable catalyst to boost the OER is of great urgency. In this work, we develop a facile strategy for the synthesis of well-defined phosphorus and fluorine co-doped Ni Co N hybrid nanorods (HNs) by using ionic liquids (ILs; 1-butyl-3-methylimidazolium hexafluorophosphate). In comparison to the IrO catalyst, the as-obtained PF/Ni Co N HNs manifests a low overpotential of 280 mV at 10 mA cm , Tafel slope of 66.1 mV dec , and excellent durability in 1.0 m KOH solution. Furthermore, the iR-corrected electrochemical results indicate it could achieve a current density of 100 mA cm at an overpotential of 350 mV. The combination of cobalt and nickel elements, 1D mesoporous nanostructure, heteroatom incorporation, and ionic liquid-assisted nitridation, which result in faster charge transfer capability and more active surface sites, can facilitate the release of oxygen bubbles from the catalyst surface. Our findings confirm that surface heteroatom doping in bimetallic nitrides could serve as a new class of OER catalyst with excellent catalytic activity.

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Section: Resultsmentioning

confidence: 99%

Phosphorus and Fluorine Co‐Doping Induced Enhancement of Oxygen Evolution Reaction in Bimetallic Nitride Nanorods Arrays: Ionic Liquid‐Driven and Mechanism Clarification

Bai

Wang

et al. 2017

Chemistry A European J

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“…Currently, transition‐metal (Fe, Co, Ni, Mn, and Mo)‐based catalysts including metal oxides,23, 24, 25, 26, 27, 28, 29, 30 hydroxides,31, 32, 33, 34, 35 phosphides,36, 37, 38, 39, 40, 41, 42 sulfides,43, 44, 45, 46, 47, 48 selenides,49, 50, 51, 52, 53, 54 and nitrides55, 56, 57, 58, 59, 60, 61, 62 have been highlighted as the most promising candidates of OER and HER electrocatalysts. Especially, layered double hydroxides (LDHs)63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85 and their derivatives (metal hydroxides, oxyhydroxides, oxides, bimetal nitrides, phosphides, sulfides, and selenides)86, 87, 88, 89, 90, 91, 92…”

Section: Introductionmentioning

confidence: 99%

Recent Progress on Layered Double Hydroxides and Their Derivatives for Electrocatalytic Water Splitting

et al. 2018

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Layered double hydroxide (LDH)‐based materials have attracted widespread attention in various applications due to their unique layered structure with high specific surface area and unique electron distribution, resulting in a good electrocatalytic performance. Moreover, the existence of multiple metal cations invests a flexible tunability in the host layers; the unique intercalation characteristics lead to flexible ion exchange and exfoliation. Thus, their electrocatalytic performance can be tuned by regulating the morphology, composition, intercalation ion, and exfoliation. However, the poor conductivity limits their electrocatalytic performance, which therefore has motivated researchers to combine them with conductive materials to improve their electrocatalytic performance. Another factor hampering their electrocatalytic activity is their large lateral size and the bulk thickness of LDHs. Introducing defects and tuning electronic structure in LDH‐based materials are considered to be effective strategies to increase the number of active sites and enhance their intrinsic activity. Given the unique advantages of LDH‐based materials, their derivatives have been also used as advanced electrocatalysts for water splitting. Here, recent progress on LDHs and their derivatives as advanced electrocatalysts for water splitting is summarized, current strategies for their designing are proposed, and significant challenges and perspectives of LDHs are discussed.

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“…Highly efficient water electrolysis generally requires high-performance electrocatalysts with low overpotential, fast kinetics, and high stability. [9][10][11] Recently, transition-metal hydroxides, [7,12] phosphides, [8,[13][14][15][16] nitrides, [17,18] and chalcogenides [19][20][21][22] have been investigated as promising candidates for bifunctional electrocatalysts. [7,8] The search for earth-abundant, lowcost HER and OER electrocatalysts that are robust, have high activity and stability has triggered numerous efforts to replace noble metal-based materials.…”

Section: Introductionmentioning

confidence: 99%

“…[9][10][11] Recently, transition-metal hydroxides, [7,12] phosphides, [8,[13][14][15][16] nitrides, [17,18] and chalcogenides [19][20][21][22] have been investigated as promising candidates for bifunctional electrocatalysts. [9,12,17,19,22,34] However, the high surface energy of sheets, which are unstable, leads to the possibility of stacking with surrounding sheets through van der Waals attractions, resulting in a decrease of the active surface area. [23][24][25][26] In addition, according to recent reports, these compounds can operate as highly efficient OER electrocatalysts and could thus be utilized as bifunctional electrocatalysts.…”

Section: Introductionmentioning

confidence: 99%

3D Architectures of Quaternary Co‐Ni‐S‐P/Graphene Hybrids as Highly Active and Stable Bifunctional Electrocatalysts for Overall Water Splitting

Song

Yoon

et al. 2018

Advanced Energy Materials

113

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Developing low-cost, highly active, and stable bifunctional electrocatalysts is a challenging issue in electrochemical water electrolysis. Building on 3D architectured electrocatalysts through structural and compositional engineering is an effective strategy to enhance catalytic activities as well as stability and durability. Herein, 3D architectures of quaternary Co-Ni-S-P compounds coupled with graphene ((Co 1−x Ni x )(S 1−y P y ) 2 /G) electrocatalysts are proposed, in which nanosheets are self-assembled to form 3D architectures with round and flat doughnut-like shapes, toward overall water splitting. Benefiting from the 3D architectures and Ni, P substitution, (Co 1−x Ni x )(S 1−y P y ) 2 /G exhibits superior electrocatalytic activities with low overpotentials of 117 and 285 mV at 10 mA cm −2 and Tafel slopes of 85 and 105 mV dec −1 for hydrogen and oxygen evolution reactions, respectively, in alkaline media. In addition, minimal increases in overpotential are observed, even after the 10 000th voltammetric cycle and continuous chronopotentiometric testing over 50-100 h, confirming the high stability and durability of (Co 1−x Ni x )(S 1−y P y ) 2 /G. When used as both cathode and anode, (Co 1−x Ni x )(S 1−y P y ) 2 /G achieves excellent overall water splitting performance with a cell potential as low as 1.65 V, reaching a current density of 10 mA cm −2 with no obvious decay after 50 h, demonstrating that (Co 1−x Ni x )(S 1−y P y ) 2 /G is an efficient bifunctional electrocatalyst for overall water splitting.

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Nanoparticle-Stacked Porous Nickel–Iron Nitride Nanosheet: A Highly Efficient Bifunctional Electrocatalyst for Overall Water Splitting

Cited by 290 publications

References 33 publications

Phosphorus and Fluorine Co‐Doping Induced Enhancement of Oxygen Evolution Reaction in Bimetallic Nitride Nanorods Arrays: Ionic Liquid‐Driven and Mechanism Clarification

Phosphorus and Fluorine Co‐Doping Induced Enhancement of Oxygen Evolution Reaction in Bimetallic Nitride Nanorods Arrays: Ionic Liquid‐Driven and Mechanism Clarification

Recent Progress on Layered Double Hydroxides and Their Derivatives for Electrocatalytic Water Splitting

3D Architectures of Quaternary Co‐Ni‐S‐P/Graphene Hybrids as Highly Active and Stable Bifunctional Electrocatalysts for Overall Water Splitting

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