2021
DOI: 10.1002/cctc.202001689
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Carbon Cloth Supported Nitrogen Doped Porous Carbon Wrapped Co Nanoparticles for Effective Overall Water Splitting

Abstract: The key to the practical application of overall water splitting is to develop high-efficient non-noble metal electrocatalysts. Herein, carbon cloth supported N-doped porous carbon wrapped Co nanoparticles (CC@Co-NPC) are constructed with high bifunctional catalytic activity toward oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in alkaline medium. Benefiting from the exposure of abundant Co active sites, and the synergistic effect between Co particles and N-doped carbon species, the CC@Co… Show more

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Cited by 10 publications
(13 citation statements)
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“…The comparison of their XPS survey spectra reconfirms the successful incorporation of S atoms within sample Co 4 Ni 1 S/CC (Figure 3a). For the oxide precursor, two C 1s peaks at 284.8 and 287.8 eV (Figure 3b) demonstrate the coexistence of C−C and CO, respectively; 42 after vulcanization, the CO signal is completely replaced by two emerging peaks of Me−C−O/N/S (286.2 eV) 43 and OC−O species (289.1 eV) 8 (Figure 3b). The vulcanization process is suggested to promote the formation of metal complexes and carbonates between NH 2 -TPA/glucosederived chars and Ni/Co ions.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…The comparison of their XPS survey spectra reconfirms the successful incorporation of S atoms within sample Co 4 Ni 1 S/CC (Figure 3a). For the oxide precursor, two C 1s peaks at 284.8 and 287.8 eV (Figure 3b) demonstrate the coexistence of C−C and CO, respectively; 42 after vulcanization, the CO signal is completely replaced by two emerging peaks of Me−C−O/N/S (286.2 eV) 43 and OC−O species (289.1 eV) 8 (Figure 3b). The vulcanization process is suggested to promote the formation of metal complexes and carbonates between NH 2 -TPA/glucosederived chars and Ni/Co ions.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…As such, the pursuit of bifunctional electrocatalysts with excellent activity and durability for both the OER and HER is hopeful to simplify the electrolyzer system, avoid mismatched HER/OER catalysts in the same electrolyte, and further lower the economic cost of water splitting. Meanwhile, abundant efforts have been made to develop low-cost alternative catalysts for the HER or OER, typically including first-row transition-metal (Ni, Co, Fe, and Mn) chalcogenides, , phosphides, carbides, nitrides, etc. To improve their sluggish HER and OER kinetics in the same electrolyte, diverse effective strategies have been developed to modify the dual-active structures by building a synergistic effect between dissimilar active species, controlling morphologies/decreasing dimension to increase utilization of active species, and applying conductive substrates to facilitate electron transfer .…”
Section: Introductionmentioning
confidence: 99%
“…[18] The broad peaks marked with asterisks at around 24°and 43°are related to (002) and (100) planes of carbon cloth. [19] With Fe content increasing, the intensity of the (003) plane enhances from Ni 0.9 Fe 0.1 CH/CC to Ni 0.7 Fe 0.3 CH/CC, meaning the crystallinity of these samples increases. [7a] Figure 1a also shows the intensity of the (113) plane enhances from Ni 0.9 Fe 0.1 CH/CC to Ni 0.7 Fe 0.3 CH/ CC.…”
Section: Resultsmentioning
confidence: 99%
“…NiFe carbonate hydroxide as an alternate to LDH system is readily available, because carbonate anions are difficult to avoid coming from CO 2 in ambient air and have high stability in LDH galleries [18] . The broad peaks marked with asterisks at around 24° and 43° are related to (002) and (100) planes of carbon cloth [19] . With Fe content increasing, the intensity of the (003) plane enhances from Ni 0.9 Fe 0.1 CH/CC to Ni 0.7 Fe 0.3 CH/CC, meaning the crystallinity of these samples increases [7a] .…”
Section: Resultsmentioning
confidence: 99%
“…is regarded as the best strategy for introducing multiactive sites. [25][26][27][28][29][30] In particular, N-doping is the most effective approach so far for preparing multiactive catalysts [23,25,31,32] owing to the versatile activity of N-atoms that comes from the geometric properties (i.e., graphitic-N, pyridinic-N, and pyrrolic-N) of the N-doped carbon catalysts. [33] The electronic nature of carbon-based materials can be tuned by doping with N-atoms, this can induce asymmetrical charge redistributions on the neighboring carbon atoms.…”
Section: Introductionmentioning
confidence: 99%