| 1. |
- Fang, Zhiyong, et al.
(författare)
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Selective Electro-oxidation of Alcohols to the Corresponding Aldehydes in Aqueous Solution via Cu(III) Intermediates from CuO Nanorods
- 2021
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Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 9:35, s. 11855-11861
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical oxidation using renewable energy is an attractive strategy that provides a sustainable and mild approach for biomass transformation. Herein, the electrocatalytic oxidation of furfuryl alcohol in an aqueous solution was investigated using CuO nanorods. Two kinds of Cu-III intermediates, namely, (CuO2)(-) and (Cu2O6)(6-), were detected on the surface of the working electrode. (Cu2O6)(6-), generated in the potential range of 1.35-1.39 V versus the reversible hydrogen electrode (RHE), induced the oxidation of furfuryl alcohol to furaldehyde with a yield of >= 98%. (CuO2)(-), generated at a potential greater than 1.39 V versus RHE, which led to the oxidation of furfuryl alcohol to 2-furoic acid with a yield of >= 99%. Furthermore, the Cu-III-catalyzed system exhibited a measure of universal applicability, wherein (Cu2O6)(6-) and (CuO2)(-) induced the highly selective electro-oxidation of benzyl alcohol, vanillyl alcohol, and 4-pyridinemethanol to yield the corresponding aldehydes and acids, respectively.
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| 2. |
- Wu, Xiujuan, et al.
(författare)
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Exploration of electrocatalytic water oxidation properties of NiFe catalysts doped with nonmetallic elements (P, S, Se)
- 2021
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Ingår i: International journal of hydrogen energy. - : Elsevier BV. - 0360-3199 .- 1879-3487. ; 46:79, s. 38992-39002
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Tidskriftsartikel (refereegranskat)abstract
- The introduction of non-metallic atoms (P, S, Se) has emerged as an effective way to improve the catalytic activity of transition metal based layered double hydroxides (LDHs) for oxygen evolution reaction. However, objective comparisons of the performance of heteroelement-doped catalysts are complicated by the lack of standardization both in the electrochemical tests and physicochemical analysis. Herein, we use a unified protocol for evaluating the catalytic activities of heteroelement-doped NiFe-LDHs and explore the reasons for the differences in their catalytic performance. Some regular results are found from comparing the properties of the heteroelement-doped catalysts: (1) the introduction of P/S/Se can optimize the redox behaviors of Ni species, which is conducive to regulating adsorption energy of intermediates and the formation of high-valent active sites; (2) the specific area of catalysts was expanded after heteroelements doping, ensuring a more favorable structure for heterogeneous catalysis; (3) All P/S/Se-doped catalysts showed better activities when compared to the original NiFe LDHs in alkaline solutions, and the catalysts doped with S showed the best performance (Se < P < S).
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| 3. |
- Wu, Xiujuan, et al.
(författare)
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Metalloid Te-Doped Fe-Based Catalysts Applied for Electrochemical Water Oxidation
- 2021
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Ingår i: CHEMISTRYSELECT. - : Wiley. - 2365-6549. ; 6:24, s. 6154-6158
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Tidskriftsartikel (refereegranskat)abstract
- Metal telluride nanocatalysts have been widely used in the catalytic reactions. However, there are few examples of electrocatalytic water oxidation with metal telluride as catalysts, especially Fe-based telluride, to the best of our knowledge, has not yet been reported. In this work, the Te-doped Fe-based catalysts (FeTex) with crystalline and amorphous nanosheet structures have been successfully synthesized by chemical vapor deposition (CVD) as well as electrodeposition (ED) on the iron foam (IF), where the latter exhibited more remarkable electrocatalytic performance towards the oxygen evolution reaction (OER) in the alkaline electrolyte, requiring the overpotential (eta) of only 264.4 mV to reach a current density of 10 mA cm(-2) with a Tafel slope of 54.2 mV dec(-1). The electrochemical study confirmed that the residual Te in ED-FeTex does play a role in promoting the catalytic activity for the electrocatalytic water oxidation.
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| 4. |
- Zhao, Ziqi, et al.
(författare)
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Molecular Engineering of Photocathodes based on Polythiophene Organic Semiconductors for Photoelectrochemical Hydrogen Generation
- 2021
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 13:34, s. 40602-40611
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Tidskriftsartikel (refereegranskat)abstract
- Organic semiconductors provide significant potentials for the construction of photoelectrochemical (PEC) cells for solar hydrogen production because of their highly tunable properties. Herein, on carbon fiber paper (CFP) surface, pyridyl (Py), and 4,4'-bipyridin-1-ium (Py-2(+)) groups were introduced into polythiophene (pTH) semiconductor by electrochemical copolymerization, respectively. After assembly with the Co(dmgBF(2))(2) type catalyst (CoB, dmgBF(2) = difluoroboryldimethylglyoximate), the CoB@Py-2(+)-pTH/CFP photocathode displayed nearly twice the photocurrent enhancement (550 mu A cm(-2) at 0.15 V vs reversible hydrogen electrode, RHE) comparing to that generated by the CoB@Py-pTH/CFP photocathode (290 mu A cm(-2) at 0.15 V vs RHE) for light-driven H-2 generation under AM 1.5 solar illumination. Investigation of the mechanism revealed that the introduction of the positively charged pyridinium groups could improve the intrinsic Co(dmgBF(2))(2) catalyst activity for the H-2 generation reaction. Meanwhile, the positively charged pyridinium groups serve as p-type dopants to increase the semiconductor bulk charge transfer rate and act as electron transfer mediators to promote the interfacial charge transfer kinetics between the catalyst and the pTH-based organic semiconductor.
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