Abstract:With attractive visible‐light response and chemical stability, CuWO4 has emerged to be a promising candidate as a photoanode for photoelectrochemical (PEC) water oxidation. In this work, we report a one‐step hydrothermal method to prepare CuWO4‐based films directly grown on a conductive glass substrate from a stable precursor solution. By controlling the reaction duration, CuWO4/WO3 heterojunctions with urchin‐like nanoarray morphology are obtained. The CuWO4/WO3 film obtained with an optimized hydrothermal re… Show more
“…also reported that colloidal WO 3 nanowires for solar water splitting and it is reached 1.96 mA cm −2 at 1.23 V RHE under AM1.5G solar irradiation [47] . WO 3 based materials displayed enhanced photo/catalytic activities due to the increasing charge separation, stability and alleviate photogenerated holes accumulation on the surface [48–52] . Nonetheless, we believe that the overall catalytic activity of WO 3 NLs‐ITO in this study is somewhat limited due to the low content of catalyst on the electrode.…”
Section: Resultsmentioning
confidence: 68%
“…[47] WO 3 based materials displayed enhanced photo/catalytic activities due to the increasing charge separation, stability and alleviate photogenerated holes accumulation on the surface. [48][49][50][51][52] Nonetheless, we believe that the overall catalytic activity of WO 3 NLs-ITO in this study is somewhat limited due to the low content of catalyst on the electrode. Our future studies will attempt to improve on these results through further fine-tuning of the BCP inclusion process for synthesising thicker and denser (in height and diameter) metal oxide structures.…”
We report the development of a multifunctional, nanostructured tungsten oxide catalytic device using block copolymer (BCP) templating, which was utilised for both the oxygen evolution reaction (OER) and epinephrine (EP) detection. The device was constructed by depositing a self-assembled BCP film atop an indium tin oxide (ITO) substrate. A tungsten precursor was then selectively coordinated into the film via liquid phase infiltration, which upon UV-ozone treatment yielded WO 3 surface nanolines (NLs) with excellent surface coverage. The resulting device was firstly investigated as a photoanode for OER. The onset overpotential of the WO 3 NLs-ITO electrode was determined to be 240 mV and 390 mV, with and without light illumination, respectively. Moreover, the applicability of the WO 3 NLs-ITO device for the electrochemical sensing of EP was explored using cyclic voltammetry and amperometry, exhibiting a linear response in a wide working range of 0.5-250 μM with a sensitivity of 0.0491 μA μM À 1 and detection limit of 0.086 μM. The device demonstrated high durability over multiple EP measurements, as well as strong anti-interference abilities versus well-known interfering compounds. Additionally, the device was successfully applied to accurately determine EP concentrations in commercial drug samples. The results of this study attest to the significant potential of BCP templating for developing low cost, high-performance electrocatalytic devices for future nanomanufacturing strategies.
“…also reported that colloidal WO 3 nanowires for solar water splitting and it is reached 1.96 mA cm −2 at 1.23 V RHE under AM1.5G solar irradiation [47] . WO 3 based materials displayed enhanced photo/catalytic activities due to the increasing charge separation, stability and alleviate photogenerated holes accumulation on the surface [48–52] . Nonetheless, we believe that the overall catalytic activity of WO 3 NLs‐ITO in this study is somewhat limited due to the low content of catalyst on the electrode.…”
Section: Resultsmentioning
confidence: 68%
“…[47] WO 3 based materials displayed enhanced photo/catalytic activities due to the increasing charge separation, stability and alleviate photogenerated holes accumulation on the surface. [48][49][50][51][52] Nonetheless, we believe that the overall catalytic activity of WO 3 NLs-ITO in this study is somewhat limited due to the low content of catalyst on the electrode. Our future studies will attempt to improve on these results through further fine-tuning of the BCP inclusion process for synthesising thicker and denser (in height and diameter) metal oxide structures.…”
We report the development of a multifunctional, nanostructured tungsten oxide catalytic device using block copolymer (BCP) templating, which was utilised for both the oxygen evolution reaction (OER) and epinephrine (EP) detection. The device was constructed by depositing a self-assembled BCP film atop an indium tin oxide (ITO) substrate. A tungsten precursor was then selectively coordinated into the film via liquid phase infiltration, which upon UV-ozone treatment yielded WO 3 surface nanolines (NLs) with excellent surface coverage. The resulting device was firstly investigated as a photoanode for OER. The onset overpotential of the WO 3 NLs-ITO electrode was determined to be 240 mV and 390 mV, with and without light illumination, respectively. Moreover, the applicability of the WO 3 NLs-ITO device for the electrochemical sensing of EP was explored using cyclic voltammetry and amperometry, exhibiting a linear response in a wide working range of 0.5-250 μM with a sensitivity of 0.0491 μA μM À 1 and detection limit of 0.086 μM. The device demonstrated high durability over multiple EP measurements, as well as strong anti-interference abilities versus well-known interfering compounds. Additionally, the device was successfully applied to accurately determine EP concentrations in commercial drug samples. The results of this study attest to the significant potential of BCP templating for developing low cost, high-performance electrocatalytic devices for future nanomanufacturing strategies.
“…[ 114–118 ] Hybridization of WO 3 with other semiconductors improves the separation of photo‐generated carriers and enhances the visible light absorption response. A variety of semiconductors have been coupled with WO 3 nanoarrays to form heterojunctions as improved photoanodes for water oxidation, including CuO (1.4 eV), [ 119 ] Fe 2 O 3 (2.0–2.2 eV), [ 115,120 ] SbSI (2.0 eV), [ 121 ] ZnIn 2 S 4 (2.0–2.4 eV), [ 122 ] CuWO 4 (2.25–2.45 eV), [ 116,123 ] BiVO 4 (2.4 eV), [ 54,124 ] CdS (2.4 eV) [ 125 ] and C 3 N 4 (2.7 eV). [ 126 ] The activities of some representative WO 3 ‐based heterojunction nanoarrays for PEC water splitting are summarized in Table 3 .…”
Section: Self‐supported Heterostructured Nanoarrays For Photoelectroc...mentioning
Growth of semiconductor heterojunction nanoarrays directly on conductive substrates represents a promising strategy toward high‐performance photoelectrodes for photoelectrochemical (PEC) water splitting. By controlling the growth conditions, heterojunction nanoarrays with different morphologies and semiconductor components can be fabricated, resulting in greatly enhanced light‐absorption properties, stabilities, and PEC activities. Herein, recent progress in the development of self‐supported heterostructured semiconductor nanoarrays as efficient photoanode catalysts for water oxidation is reviewed. Synthetic methods for the fabrication of heterojunction nanoarrays with specific compositions and structures are first discussed, including templating methods, wet chemical syntheses, electrochemical approaches and chemical vapor deposition (CVD) methods. Then, various heterojunction nanoarrays that have been reported in recent years based on particular core semiconductor scaffolds (e.g., TiO2, ZnO, WO3, Fe2O3, etc.) are summarized, placing strong emphasis on the synergies generated at the interface between the semiconductor components that can favorably boost PEC water oxidation. Whilst strong progress has been made in recent years to enhance the visible‐light responsiveness, photon‐to‐O2 conversion efficiency and stability of photoanodes based on heterojunction nanoarrays, further advancements in all these areas are needed for PEC water splitting to gain any traction alongside photovoltaic‐electrochemical (PV‐EC) systems as a viable and cost‐effective route toward the hydrogen economy.
“…In addition to the increased carrier concentration noted by the above papers, Guo et al ascribed the improvement of PEC performance of CuWO 4 to the reduced activation energy of the water splitting reaction after the formation of oxygen vacancies on the surface of the photoanode . Different from doping and oxygen vacancies, constructing a heterojunction is a strategy for promoting the separation of photogenerated electron and hole pairs by forming a built-in electric field. − The CuWO 4 /BiVO 4 type II heterojunction, CuWO 4 /Mn 3 O 4 p–n junction, and WO 3 /CuWO 4 heterojunction ,,− were constructed, and a built-in electric field is formed because of the difference between the semiconductors. In addition, there are numerous studies to improve charge separation at the interface by loading cocatalysts on the surface.…”
Hydrogen generation through photoelectrochemical (PEC) technology is one of the most appropriate ways for delivering sustainable fuel. Simultaneously, anisotropic properties will be exhibited by the materials with low crystal symmetry, allowing the tuning of the PEC properties by controlling the crystallographic orientation and exposed facets. Therefore, we synthesized copper tungstate films (CuWO 4 ) with highly exposed (100) crystal facets by regulating anions in the precursor solution. According to experimental characterization and density functional theory calculations, the CuWO 4 film with a high exposure ratio of the (100) crystal facet has promoted charge transport with trapfree mode and reduced recombination of electrons and holes. Meanwhile, the oxygen evolution reaction is promoted on the (100) facet because of the relatively low energy barrier. Compared to the CuWO 4 with other mixed exposure facets, CuWO 4 with a highly exposed (100) facet presents a twofold current density (0.38 mA/cm 2 ) and one-fifteenth electron transit time (0.698 ms) and also has great stability (more than 6 h). These results provide an easy way to enhance the PEC performance by modulating the exposure facets of the film electrode.
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