Abstract:The
development of photocatalysts toward highly efficient H2 evolution reactions is a feasible strategy to achieve the
effective conversion of solar energy and meet the increasing demand
for new energy. To this end, we prepared two different CdS–MoS2 photocatalysts with unique morphologies ranging from hexagonal
prisms to tetragonal nanotubes by carefully tuning polyoxometalate
synthons. These two photocatalysts, namely, CdS–MoS2-1 and CdS–MoS2-2, both exhibited remarkable photocatalytic
efficiency in H2 gener… Show more
“…CV measurements of CCO and NCS were carried out under different sweep speeds (Figure S5). By observing the image, it can be clearly seen that the CV curve of CCO has a pair of redox peaks in the potential window range of 0–0.45 V, indicating that the specific capacitance is mainly provided by the redox reactions of Co 2+ /Co 3+ /Co 4+ and Cu 2+ /Cu + with OH − ions, which are represented as follows: [2,35] …”
Section: Resultsmentioning
confidence: 99%
“…CV measurements of CCO and NCS were carried out under different sweep speeds (Figure S5). By observing the image, it can be clearly seen that the CV curve of CCO has a pair of redox peaks in the potential window range of 0-0.45 V, indicating that the specific capacitance is mainly provided by the redox reactions of Co 2 + /Co 3 + /Co 4 + and Cu 2 + /Cu + with OH À ions, which are represented as follows: [2,35] CuCo…”
Section: Resultsmentioning
confidence: 99%
“…As a promising rechargeable energy storage device, supercapacitors have attracted tremendous attention due to the excellent charge storage capacity, fast recharge ability, high power density and long service life [1–4] . The preparation of electrode materials with excellent electrochemical performance is the key factor to obtain high energy density supercapacitor.…”
Section: Introductionmentioning
confidence: 99%
“…As a promising rechargeable energy storage device, supercapacitors have attracted tremendous attention due to the excellent charge storage capacity, fast recharge ability, high power density and long service life. [1][2][3][4] The preparation of electrode materials with excellent electrochemical performance is the key factor to obtain high energy density supercapacitor. Recently, binary transition metal oxides (BTMO), such as CuCo 2 O 4 , [5] ZnCo 2 O 4 [6] and NiMoO 4 [7] have been considered to be the promising candidates as electrodes owing to their multiple redox reactions and high electrical conductivity.…”
It is an effective way to prepare multi‐dimensional and multicomponent electrode material to enhance the capacitance of supercapacitors. The multi‐dimensional micro CuCo2O4/nano NiCo2S4 structure was synthesized by wrapping NiCo2S4 nanosheets on urchin‐like CuCo2O4 microspheres on the surface of nickel foam by two‐step hydrothermal method, and then electrochemical deposition. Due to the synergistic effect of the one‐dimensional CuCo2O4 and the two‐dimensional NiCo2S4 composite and its especial three‐dimensional core‐shell structure, the composite electrode shows excellent supercapacitor performance. The CuCo2O4@NiCo2S4 with three electrodeposition cycles (CCO@NCS‐3) exhibits a high specific capacitance of 2283.3 F g−1 at 1 A g−1, good rate capability (79.9 % capacitance retention at 10 A g−1) and cycling stability of 84.0 % over 3000 cycles. All these results indicate that the concepts of multi‐dimensional and multi‐component integration provide a general approach for the development of high‐performance materials.
“…CV measurements of CCO and NCS were carried out under different sweep speeds (Figure S5). By observing the image, it can be clearly seen that the CV curve of CCO has a pair of redox peaks in the potential window range of 0–0.45 V, indicating that the specific capacitance is mainly provided by the redox reactions of Co 2+ /Co 3+ /Co 4+ and Cu 2+ /Cu + with OH − ions, which are represented as follows: [2,35] …”
Section: Resultsmentioning
confidence: 99%
“…CV measurements of CCO and NCS were carried out under different sweep speeds (Figure S5). By observing the image, it can be clearly seen that the CV curve of CCO has a pair of redox peaks in the potential window range of 0-0.45 V, indicating that the specific capacitance is mainly provided by the redox reactions of Co 2 + /Co 3 + /Co 4 + and Cu 2 + /Cu + with OH À ions, which are represented as follows: [2,35] CuCo…”
Section: Resultsmentioning
confidence: 99%
“…As a promising rechargeable energy storage device, supercapacitors have attracted tremendous attention due to the excellent charge storage capacity, fast recharge ability, high power density and long service life [1–4] . The preparation of electrode materials with excellent electrochemical performance is the key factor to obtain high energy density supercapacitor.…”
Section: Introductionmentioning
confidence: 99%
“…As a promising rechargeable energy storage device, supercapacitors have attracted tremendous attention due to the excellent charge storage capacity, fast recharge ability, high power density and long service life. [1][2][3][4] The preparation of electrode materials with excellent electrochemical performance is the key factor to obtain high energy density supercapacitor. Recently, binary transition metal oxides (BTMO), such as CuCo 2 O 4 , [5] ZnCo 2 O 4 [6] and NiMoO 4 [7] have been considered to be the promising candidates as electrodes owing to their multiple redox reactions and high electrical conductivity.…”
It is an effective way to prepare multi‐dimensional and multicomponent electrode material to enhance the capacitance of supercapacitors. The multi‐dimensional micro CuCo2O4/nano NiCo2S4 structure was synthesized by wrapping NiCo2S4 nanosheets on urchin‐like CuCo2O4 microspheres on the surface of nickel foam by two‐step hydrothermal method, and then electrochemical deposition. Due to the synergistic effect of the one‐dimensional CuCo2O4 and the two‐dimensional NiCo2S4 composite and its especial three‐dimensional core‐shell structure, the composite electrode shows excellent supercapacitor performance. The CuCo2O4@NiCo2S4 with three electrodeposition cycles (CCO@NCS‐3) exhibits a high specific capacitance of 2283.3 F g−1 at 1 A g−1, good rate capability (79.9 % capacitance retention at 10 A g−1) and cycling stability of 84.0 % over 3000 cycles. All these results indicate that the concepts of multi‐dimensional and multi‐component integration provide a general approach for the development of high‐performance materials.
“…For example, Ran et al developed a Si-doped ZnWO 4 @ZnO photocatalyst with a unique morphology from a Keggin POMs@ZIF precursor that acted as an efficient catalyst for degrading Rhodamine B under visible light irradiation . Recently, Sun et al reported the synthesis of CdS-MoS 2 with different morphologies under different synthetic conditions starting from the H 3 PMo 12 O 40 cluster and studied the effects of morphology on their photocatalytic hydrogen evolution activities . These new photocatalysts showed superior performance toward the hydrogen evolution reaction (HER) compared to the conventional CdS.…”
Heterogeneous photocatalysis is a convenient and effective tool for eliminating toxic organic effluents from the textile and pharmaceutical industries. The analogous photocatalytic properties of polyoxometalates (POMs) with metal oxide-based semiconductors make them applicable for photocatalytic wastewater treatment applications. However, the high aqueous solubility and low coverage of the visible solar spectrum limit the wider applicability of traditional POMs as heterogeneous photocatalysts. Herein, we report, for the first time, the hydrothermal transformation of a UV-active polyoxometalate precursor, (C 16 H 36 N) 4 [Mo 8 O 26 ] abbreviated as TBA-Mo8, into a visible light active photocatalytic carbon-doped Bi 2 MoO 6 nanosheets (C-BMO) in the presence of a Bi 3+ salt and studied its catalytic activities toward the degradation of a dye pollutant, malachite green (MG), and a pharmaceutical pollutant, ciprofloxacin (CF). For comparison purposes, an undoped Bi 2 MoO 6 (U-BMO) nanosheet was also prepared under identical conditions starting from an in situ generated POM precursor H 4 [Mo 8 O 26 ]. The successful transformation of TBA-Mo8 and H 4 [Mo 8 O 26 ] into Bi 2 MoO 6 photocatalysts under hydrothermal conditions was confirmed through a series of analytical and spectroscopic techniques, including Fourier transform infrared, Raman, X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron spectroscopy, highresolution transmission electron spectroscopy, and other analyses. The results of the photocatalytic experiments revealed superior catalytic activities of C-BMO compared to U-BMO and the parent cluster TBA-Mo8 under visible light irradiation. C-BMO achieved 70 and 87% degradation of MG and CF under visible light irradiation against the 29 and 35% degradation, respectively, shown by U-BMO. A plausible reason for the higher photocatalytic activity of C-BMO is its better charge separation due to the band gap modification resulting from carbon doping. The detailed pathways of MG and CF degradation have also been proposed based on scavenger studies and ESI-MS analyses of the photocatalytic degradation products. This work, therefore, summarizes how simple polyoxometalate can serve as precursors for developing better and more efficient visible light active photocatalysts under milder experimental procedures.
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