Bulk metal doping and surface phosphate modification were synergically adopted in a rational design to upgrade the CeO catalyst, which is highly active but easily deactivated for the catalytic oxidation of chlorinated volatile organic compounds (Cl-VOCs). The metal doping increased the redox ability and defect sites of CeO, which mostly promoted catalytic activity and inhibited the formation of dechlorinated byproducts but generated polychlorinated byproducts. The subsequent surface modification of the metal-doped CeO catalysts with nonmetallic phosphate completely suppressed the formation of polychlorinated byproducts and, more importantly, enhanced the stability of the surface structure by forming a chainmail layer. A highly active, durable, and selective catalyst of phosphate-functionalized RuO-CeO was the most promising among all the metal-doped (Ru, Pd, Pt, Cr, Mn, Fe, Co, and Cu) CeO catalysts investigated owing to the prominent chemical stability of RuO and its superior versatility in the catalytic oxidation of different kinds of Cl-VOCs and other typical pollutants, including dimethyl sulfide, CO, and CH. Moreover, the chemical stability of the catalyst, including its bulk and surface structural stability, was investigated by combining intensive treatment with HCl/HO or HCl with subsequent ex situ ultraviolet-visible light Raman spectroscopy and confirmed the superior resistance to Cl poisoning of the phosphate-functionalized RuO-CeO. This work exemplifies a promising strategy for developing ideal catalysts for the removal of Cl-VOCs and provides a catalyst with the superior catalytic performance in Cl-VOC oxidation to date.
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http://dx.doi.org/10.1021/acs.est.0c08256 | DOI Listing |
Chempluschem
December 2024
Qinghai University, Mechanical Engineering, Qinghai,China, 810016, Qinghai province, CHINA.
Due to the high catalytic activity and stability for oxygen reduction reaction, N-coordinated Fe-Cu dual-metal doped carbon material (FeCu-N-C) is considered to be one of the promising electrode materials for metal-air battery and fuel cells. Herein, FeCu-N-C dual-metal catalysts was synthesized by an adsorption-calcination strategy. The prepared FeCu-N-C exhibited high activity and stability both in alkaline and acidic media.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Donghua University - Songjiang Campus: Donghua University, College of chemistry, chemical engineering and biotechnology, 2999 Renmin North Road, Shanghai, 201620, Shanghai, CHINA.
Developing new organic radical emission systems and regulating their luminescence properties presents a significant challenge. Herein, we build dynamic and multi-emission band radical luminescence systems by co-assembling inorganic metal salts with carbonyl compounds in ionic liquids. After the assembling, dual-band, and excitation wavelength-dependent emission was observed upon light irradiation, one emission band originates from carbonyl radical after light irradiation, the other band from the ligand-metal charge transfer (LMCT) state, which benefits from the charge transfer from the radicals to the metal salts.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Fudan University, Department of Chemistry, Institute of Biomedical Sciences, Handan road, 200433, Shanghai, CHINA.
Electrochemiluminescence (ECL) microscopy has emerged as a powerful technique for single-cell imaging owing to its unparalleled background-free imaging advantages. However, controlled intracellular ECL imaging remains challenging. Here, we developed a stimuli-responsive self-assembled DNA nanomachine that enables the ECL imaging of intracellular target biomolecules in single cells.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
Institute of Theoretical and Applied Research, Duy Tan University, Ha Noi 100000, Vietnam.
The absence of intrinsic magnetism in two-dimensional (2D) materials demands functionalization as necessary for broadening their applications. In this work, doping with transition metals (Mn and Fe) is proposed to modify the electronic and magnetic properties of a GeS monolayer. A pristine monolayer is an indirect gap semiconductor with an energy gap of 0.
View Article and Find Full Text PDFSmall Methods
December 2024
Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing, 100084, China.
Modifying the redox properties of transition metals within layered cathode materials represents a pivotal approach in the pursuit of high-performance cathode materials. The recent research has revealed a novel finding: the introduction of Mg into LiNiCoMnO leads to a shift in the oxidation sequence of transition metals during lithium extraction, with Co supplanting Ni as the primary oxidized species during the initial stages of lithium extraction. This alteration in the lattice constants and volume, among other structural parameters, serves to mitigate lattice stress during the charging and discharging cycles.
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