The rational structure design and controllable surface modification of electrode materials plays a decisive role in constructing high performance energy storage and conversion devices. Herein, the P-doped cobalt carbonate hydroxide@NiMoO (P-CoCH@NiMoO) nanowires@nanosheets double-shell hierarchical structure is successfully fabricated on nickel foam. The unique nanowire@nanosheet structure with gradient porous distribution and hydrophilic nature can facilitate both the charge and electron transfer based on the synergetic effects with conductive NiMoO array. Importantly, the dopant of P element can enrich oxygen vacancies on the surface of CoCH nanowire, thus increase the effective active sites and enhance the electrocatalytic performance. Therefore, when act as the supercapacitor electrode, the bi-functional P-CoCH@NiMoO/NF material achieves high areal capacitance (5.08 F cm at 2 mA cm, 0.75 mAh cm) and good cyclic stability (82.7% capacitance retention after 2000 cycles). Meanwhile, when utilize as the hydrogen evolution electrode in alkaline solution, a low overpotential (115 mV at 10 mA cm) and Tafel slope (113.5 mV dec) can also be achieved.
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http://dx.doi.org/10.1016/j.jcis.2020.11.046 | DOI Listing |
J Colloid Interface Sci
February 2025
Fujian Provincial Key Laboratory of Photoelectric Functional Materials, College of Materials Science and Engineering, Huaqiao University, Xiamen 361021, China; MOE Engineering Research Center for Environmentally Friendly Functional Materials, Institute of Materials Physical Chemistry, Huaqiao University, Quanzhou 362021, China. Electronic address:
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September 2024
College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, China.
Water electrolysis has become an attractive hydrogen production method. Oxygen evolution reaction (OER) is a bottleneck of water splitting as its four-electron transfer procedure presents sluggish reaction kinetics. Designing composite catalysts with high performance for efficient OER still remains a huge challenge.
View Article and Find Full Text PDFDalton Trans
June 2024
Department of Biology, Xinzhou Normal University, Xinzhou 034000, China.
Small
October 2024
College of Aerospace Science and Engineering, National University of Defense Technology, Changsha, 410073, China.
High voltage cobalt-free spinel LiNiMnO (LNMO) is well organized as a high-power cathode material for lithium (Li)-ion batteries, however, the weak interaction between the 3d orbital of the transition metal (TM) ions and the 2p orbital of oxygen (O) leads to the instability of crystal structural, hindering the long-term stable cycling of LNMO cathode especially at high temperatures. Here, a design strategy of orbital interaction is initiated to strengthen TM 3d-O 2p framework in P-doped LNMO (P-LNMO) by choosing phytic acid as P dopant, which can realize more uniform doping compared to regular phosphate. The results show that the enhancement of TM 3d-O 2p orbital interaction in P-LNMO can suppress the Jahn-Teller effect and subsequent dissolution of Mn, as well as lowers the energy barrier for Li ion insertion/extraction kinetics.
View Article and Find Full Text PDFLangmuir
June 2024
Fujian Provincial Key Laboratory of Biomass Low-Carbon Conversion, Institute of Advanced Carbon Conversion Technology, College of Chemical Engineering, Huaqiao University, Xiamen, Fujian 361021, China.
The electrooxidation of 5-hydroxymethylfurfural (HMF) into 2,5-furandicarboxylic acid (FDCA) demonstrated its unique superiority, not only in reducing overpotential and improving energy conversion efficiency for green hydrogen production but also in utilizing abundant biomass resources and producing high-value-added chemicals. However, designing highly efficient electrocatalysts for HMF electrooxidation (HMF-EOR) with low cost and high performance for large-scale production remained a huge challenge. Herein, we introduced an easy one-step activation process to produce P-doped porous biochar loaded with multiple crystal surfaces exposed to CoPO catalysts (CoPO@PC), which exhibited outstanding electrooxidation performance.
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