2015
DOI: 10.1016/j.apsusc.2015.08.150
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Fabrication of the heterostructured CsTaWO6/Au/g-C3N4 hybrid photocatalyst with enhanced performance of photocatalytic hydrogen production from water

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Cited by 56 publications
(11 citation statements)
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“…Furthermore, Figure c–f shows the high-resolution spectra of C 1s, N 1s, B 1s, and Ni 2p. The strong peak at 284.6 eV in Figure c is attributed to C–C coordination of standard reference carbon, and the peaks at 285.1 and 288.3 eV correspond to the C–(N)­3 group and C–N–C, respectively. , The strong peak appearing in the high-resolution image of N 1s as shown in Figure d presents the N-replaced aromatic rings (C–NC), and peaks ascribed to tertiary nitrogen groups (N–(C)­3) and charging effects can be found at 401.2 and 404.3 eV, respectively. , The peak at 399.9 eV (C–BN 2 groups) demonstrates that some boron atoms are brought into the g-C 3 N 4 frame. , As shown in Figure e, B 1s can be deconvoluted into three peaks with binding energies at 190.1, 191.8, and 192.8 eV. The binding energy at 190.1 eV corresponds to h-BN groups .…”
Section: Resultsmentioning
confidence: 97%
“…Furthermore, Figure c–f shows the high-resolution spectra of C 1s, N 1s, B 1s, and Ni 2p. The strong peak at 284.6 eV in Figure c is attributed to C–C coordination of standard reference carbon, and the peaks at 285.1 and 288.3 eV correspond to the C–(N)­3 group and C–N–C, respectively. , The strong peak appearing in the high-resolution image of N 1s as shown in Figure d presents the N-replaced aromatic rings (C–NC), and peaks ascribed to tertiary nitrogen groups (N–(C)­3) and charging effects can be found at 401.2 and 404.3 eV, respectively. , The peak at 399.9 eV (C–BN 2 groups) demonstrates that some boron atoms are brought into the g-C 3 N 4 frame. , As shown in Figure e, B 1s can be deconvoluted into three peaks with binding energies at 190.1, 191.8, and 192.8 eV. The binding energy at 190.1 eV corresponds to h-BN groups .…”
Section: Resultsmentioning
confidence: 97%
“…It is generally believed that the co‐catalysts as traps can extract the energetic enough electrons and holes that migrate to the surface of the semiconductor without recombination, provide reaction active sites, stimulate the elctrocatalytic reduction and oxidation of the reactants adsorbed on their surface with the lowered overpotentials, and further decrease the activation energy for gas evolution . So far, various types of H 2 ‐evolution co‐catalysts, including noble metals/alloys (Pt, Au, Ag), graphene, earth‐abundant transition metals and their composites (e.g., Ni, MoS 2 , WS 2 , NiS x , CoS x , CoO x , Ni 2 P, NiO x , and Ni(OH) 2 ) have been available for different semiconductors, which generally exhibit very low electrochemical H 2 ‐evolution onset overpotentials (<−0.4 V). Meanwhile, the noble metal based oxides (e.g., RuO 2 , IrO x ), cost‐acceptable cobalt based species (e.g., CoO x , Co(II), Co(OH) 2 , Nocera Co–Pi), MnO x FeOOH, and NiOOH have been demonstrated to be excellent water‐oxidation co‐catalysts to boost the photocatalytic O 2 evolution over different semiconductors.…”
Section: Fundamental Mechanism Of Heterogeneous Photocatalysismentioning
confidence: 99%
“…The CB of CsTaWO 6 is composed of the W 5d and Ta 5d hybrid orbitals, while the VB is mainly contributed by O 2p orbitals [43]. Attractively, the CB of CsTaWO 6 is located at approximately − 0.37 V vs. NHE [222], indicating that the photogenerated electrons in CsTaWO 6 have sufficient reductive potential for the hydrogen production. However, the bandgap of CsTaWO 6 is as large as 3.8 eV [43], which limits the light absorption in a very narrow UV range.…”
Section: Quaternary Oxidesmentioning
confidence: 99%