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We have successfully integrated a covalently bonded hydrogen evolving catalyst (Complex A) into a highly stable photosensitizable UiO-MOF by a facile click reaction synthesis.
We have successfully integrated a covalently bonded hydrogen evolving catalyst (Complex A) into a highly stable photosensitizable UiO-MOF by a facile click reaction synthesis.
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A facial cobalt(III) polypyridyl complex was characterized by several spectroscopic and electrochemical techniques and utilized as a robust hydrogen evolving catalyst in both organic and aqueous media.
A facial cobalt(III) polypyridyl complex was characterized by several spectroscopic and electrochemical techniques and utilized as a robust hydrogen evolving catalyst in both organic and aqueous media.
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10.1016/j.expthermflusci.2020.110316
Bubble behavior in a hydrogen evolving system was compared to that under boiling conditions.
Bubble behavior in a hydrogen evolving system was compared to that under boiling conditions.
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10.1595/205651322x16269403109779
Here, a series of hydrogen evolving photocatalysts based on a ruthenium(II) bipyridyl sensitiser covalently linked to Pt or Pd catalytic centres were adsorbed onto mesoporous NiO and tested for hydrogen evolution in a photoelectrochemical half-cell.
Here, a series of hydrogen evolving photocatalysts based on a ruthenium(II) bipyridyl sensitiser covalently linked to Pt or Pd catalytic centres were adsorbed onto mesoporous NiO and tested for hydrogen evolution in a photoelectrochemical half-cell.
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10.1021/acs.inorgchem.1c00900
The hydrogen evolving activity of the materials was explored in pH 1.
The hydrogen evolving activity of the materials was explored in pH 1.
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10.1080/00958972.2021.1918339
The hydrogen evolving mechanism is discussed and the complexes are compared to their non-alkylated analogs using DFT calculations.
The hydrogen evolving mechanism is discussed and the complexes are compared to their non-alkylated analogs using DFT calculations.
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10.1016/J.APCATB.2021.120091
Under minimally optimized conditions, the resulting POM@MOF composites can effectively photocatalyze hydrogen production with superior long-term stability and reusability, achieving a hydrogen evolving rate of 3482 and 13051 μmol g−1 h−1 for Ni3PW10@NU-1000 and Ni3P2W16@NU-1000, respectively.
Under minimally optimized conditions, the resulting POM@MOF composites can effectively photocatalyze hydrogen production with superior long-term stability and reusability, achieving a hydrogen evolving rate of 3482 and 13051 μmol g−1 h−1 for Ni3PW10@NU-1000 and Ni3P2W16@NU-1000, respectively.
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10.1016/J.NANOEN.2021.106402
Benefitting from high density reactive sites and fluent mass transfer as a result of trimodal porous architecture and strong electronic modulation from NiZn intermetallic, TMP NiZn-Ni/NF primely overcomes the sluggish hydrogen evolving kinetics with superior catalytic performances comparable to Pt/C and many other reported similar electrocatalysts.
Benefitting from high density reactive sites and fluent mass transfer as a result of trimodal porous architecture and strong electronic modulation from NiZn intermetallic, TMP NiZn-Ni/NF primely overcomes the sluggish hydrogen evolving kinetics with superior catalytic performances comparable to Pt/C and many other reported similar electrocatalysts.
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10.1016/J.APCATB.2019.117979
We have successfully integrated a covalently bonded hydrogen evolving catalyst (Complex A) into a highly stable photosensitizable UiO-MOF by a facile click reaction synthesis.
We have successfully integrated a covalently bonded hydrogen evolving catalyst (Complex A) into a highly stable photosensitizable UiO-MOF by a facile click reaction synthesis.
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10.1016/J.POLY.2018.11.053
A facial cobalt(III) polypyridyl complex was characterized by several spectroscopic and electrochemical techniques and utilized as a robust hydrogen evolving catalyst in both organic and aqueous media.
A facial cobalt(III) polypyridyl complex was characterized by several spectroscopic and electrochemical techniques and utilized as a robust hydrogen evolving catalyst in both organic and aqueous media.
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10.1016/J.JPOWSOUR.2018.12.034
50 mA cm−2 owing to superior charge transport in hybrid photocathode as compared to pristine Si nanowires for hydrogen evolving reaction at pH∼7.
50 mA cm−2 owing to superior charge transport in hybrid photocathode as compared to pristine Si nanowires for hydrogen evolving reaction at pH∼7.
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10.1039/C9TA01220F
1)-textured polycrystalline WSe2 films are developed as hydrogen evolving photoelectrodes and improved through deposition of a thin ammonium thiomolybdate (NH4)2Mo3S13 catalyst film.
1)-textured polycrystalline WSe2 films are developed as hydrogen evolving photoelectrodes and improved through deposition of a thin ammonium thiomolybdate (NH4)2Mo3S13 catalyst film.
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10.1016/J.APSUSC.2019.03.250
The resulting ip-CoP/CF demonstrates improved hydrogen evolving efficiency in both acidic and alkaline conditions.
The resulting ip-CoP/CF demonstrates improved hydrogen evolving efficiency in both acidic and alkaline conditions.
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10.3389/fenrg.2019.00139
It is concluded that the water CHF condition can be simulated by the non-heating hydrogen evolving system.
It is concluded that the water CHF condition can be simulated by the non-heating hydrogen evolving system.
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10.1021/jacs.9b07084
Being one of the very few hydrogen evolving electrocatalytic MOFs based on a redox-active metallo-linker, this work explores uncharted terrain for greater catalyst diversity and charge transport pathways.
Being one of the very few hydrogen evolving electrocatalytic MOFs based on a redox-active metallo-linker, this work explores uncharted terrain for greater catalyst diversity and charge transport pathways.
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