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      Fast fabrication of self-supported porous nickel phosphide foam for efficient, durable oxygen evolution and overall water splitting

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          Abstract

          Self-supported porous Ni–P foam is fabricated by a convenient one-step method, and exhibits excellent electrocatalytic performance towards oxygen evolution reaction. An alkaline electrolyzer constructed using two self-supported porous Ni–P foams shows superior energy efficiency of 90.2% at 10 mA cm −2, and can sustain 1000 h under operation conditions without obvious degradation.

          Abstract

          Self-supported three-dimensional porous nickel phosphide (Ni–P) foam has been fabricated by exposing commercially available Ni foam in phosphorus vapor at an elevated temperature for a short period of time. The as-fabricated Ni–P foam consists of Ni 2P skeletons covered with vertically aligned Ni 5P 4–NiP 2 nanosheets. When used as a self-supported anode to catalyze the oxygen evolution reaction (OER), it exhibits exceptionally high catalytic current density (191.0 mA cm −2 at an overpotential of η = 0.35 V) and outstanding long-term stability and durability (affording 10 mA cm −2 at 1.45 V vs. RHE for 26 h without degradation). Scanning electron microscopy, transmission electron microscopy, and X-ray diffractometry analyses show that during the galvanostatic OER electrolysis the surface Ni–P nanosheets are transformed to nickel oxide/hydroxide (NiO/Ni(OH) x), forming a Ni–P/NiO(Ni(OH) x) heterojunction on ligament surfaces of the porous Ni–P foam which would enhance the OER performance. The synergistic effect between Ni–P and NiO/Ni(OH) x is also confirmed by control experiments with self-supported NiO and Ni(OH) 2 nanosheet electrodes. An alkaline electrolyzer has been built using two identical self-supported porous Ni–P foams as the anode and cathode, respectively. The electrolyzer exhibits superior electrolysis efficiency of 90.2% at 10 mA cm −2, and can maintain sufficiently high efficiency of 72.2% even at 100 mA cm −2. Moreover, the electrolyzer is substantially durable when working at 10 and 20 mA cm −2, splitting water constantly up to 1000 h with only a minor variation in the cell's voltage. The self-supported porous Ni–P foam holds substantial promise for use as both cathode and anode in industrial alkaline water electrolyzers.

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          A perovskite oxide optimized for oxygen evolution catalysis from molecular orbital principles.

          The efficiency of many energy storage technologies, such as rechargeable metal-air batteries and hydrogen production from water splitting, is limited by the slow kinetics of the oxygen evolution reaction (OER). We found that Ba(0.5)Sr(0.5)Co(0.8)Fe(0.2)O(3-δ) (BSCF) catalyzes the OER with intrinsic activity that is at least an order of magnitude higher than that of the state-of-the-art iridium oxide catalyst in alkaline media. The high activity of BSCF was predicted from a design principle established by systematic examination of more than 10 transition metal oxides, which showed that the intrinsic OER activity exhibits a volcano-shaped dependence on the occupancy of the 3d electron with an e(g) symmetry of surface transition metal cations in an oxide. The peak OER activity was predicted to be at an e(g) occupancy close to unity, with high covalency of transition metal-oxygen bonds.
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            An advanced Ni-Fe layered double hydroxide electrocatalyst for water oxidation.

            Highly active, durable, and cost-effective electrocatalysts for water oxidation to evolve oxygen gas hold a key to a range of renewable energy solutions, including water-splitting and rechargeable metal-air batteries. Here, we report the synthesis of ultrathin nickel-iron layered double hydroxide (NiFe-LDH) nanoplates on mildly oxidized multiwalled carbon nanotubes (CNTs). Incorporation of Fe into the nickel hydroxide induced the formation of NiFe-LDH. The crystalline NiFe-LDH phase in nanoplate form is found to be highly active for oxygen evolution reaction in alkaline solutions. For NiFe-LDH grown on a network of CNTs, the resulting NiFe-LDH/CNT complex exhibits higher electrocatalytic activity and stability for oxygen evolution than commercial precious metal Ir catalysts.
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              Ni2P as a Janus catalyst for water splitting: the oxygen evolution activity of Ni2P nanoparticles

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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2016
                2016
                : 4
                : 15
                : 5639-5646
                Affiliations
                [1 ]International Iberian Nanotechnology Laboratory (INL)
                [2 ]4715-330 Braga
                [3 ]Portugal
                Article
                10.1039/C5TA10317G
                ad212b26-a57b-43c3-ad35-bb26bcf22384
                © 2016
                History

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