We report the successful synthesis of Mo doped NiP nanowires (NWs) on a Ni foam (NF) substrate by a two-step strategy, which could be used as an efficient and stable hydrogen evolution reaction (HER) electrocatalyst over the whole pH range (0-14). Electrochemical investigations demonstrated that Mo doping made the catalytic activity of NiP significantly enhanced. To achieve a current density of 10 mA cm, Mo-NiP NWs/NF required an overpotential of 67 mV in acidic solution, 78 mV in alkaline solution and 84 mV in neutral solution. It also showed superior stability with negligible activity decay after its use in the HER under different pH conditions for 24 h. Such excellent HER activity might originate from the synergistic effect between molybdenum (Mo) and nickel (Ni) atoms. The present work provides a valuable route for the design and synthesis of inexpensive and efficient all-pH HER electrocatalysts.
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http://dx.doi.org/10.1039/c7nr03515b | DOI Listing |
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December 2024
Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, P. R. China.
Replacing the oxygen evolution reaction with the alternative glycerol electro-oxidation reaction (GER) provides a promising strategy to enhance the efficiency of hydrogen production via water electrolysis while co-generating high-value chemicals. However, obtaining low-cost and efficient GER electrocatalysts remains a big challenge. Herein, a self-supported N-doped CoNiO nanoflakes (N-CoNiO NF) is proposed for efficient electrocatalytic oxidation of glycerol to formate.
View Article and Find Full Text PDFInorg Chem
December 2024
School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018, China.
The two-electron oxygen reduction reaction (2e ORR) for electrochemical hydrogen peroxide (HO) synthesis has drawn much attention due to its eco-friendly, cost-effective, and highly efficient properties. Developing catalysts with excellent HO production rates and selectivity is still a big challenge. In this work, an iron-doped nickel phosphide (Fe-Ni-P) catalyst was synthesized by a solvent thermal method.
View Article and Find Full Text PDFJ Chem Phys
November 2024
State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350108, People's Republic of China.
The CO reduction reaction (CORR) for the production of high-value-added multi-carbon (C2+) products is currently being actively investigated, where searching for high-efficiency catalysts with moderate CO intermediate binding strength and low kinetic barrier for C-C coupling poses a significant challenge. In this study, we employed density functional theory computations to design four synergistic coupling dual sites catalysts for CORR to C2 products, namely, TM-P@melon, by co-doping transition metals (TM = Mn, Fe, Co, and Ni) and phosphorus (P) into the polymeric carbon nitride (i.e.
View Article and Find Full Text PDFAdv Sci (Weinh)
November 2024
Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, Warsaw, 01-224, Poland.
The enhancement of the photovoltaic performance upon the aging process at particular environment is often observed in perovskite solar cells (PSCs), particularly for the devices with 2,2',7,7'-tetrakis(N,N-di(4-methoxyphenyl)amino)-9,9'-spirobifluorene (spiro-OMeTAD) as hole transporting material (HTM). In this work, for the first time the effect of aging the typical n-i-p PSCs employing nickel phthalocyanine (coded as Bis-PF-Ni) solely as dopant-free HTM is investigated and as an additive in spiro-OMeTAD solution. This study reveals that the prolong aging of these devices at dry air condition (RH = 2%, 25 °C) is beneficial for the improvement of their performances.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2024
School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.
In this study, a series of dopant-free, low-cost hole-transporting materials (HTMs) based on triphenylamine-functionalized azadipyrromethene dyes (TPA-ADPs ) were designed and synthesized. The properties of these new HTMs were investigated by optical spectroscopy, cyclic voltammetry, thermogravimetric analysis, differential scanning calorimetric, atomic force microscopy, and X-ray diffraction, as well as theoretical calculations. The results indicated that the TPA-ADPs presented well-matched energy levels with perovskite, higher hole mobility, as well as more effective defect passivation at the perovskite/HTM interface by the coordination interaction between the ADP moiety and the undercoordinated Pb.
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