Opportunities and Challenges in Precise Synthesis of Transition Metal Single-Atom Supported by 2D Materials as Catalysts toward Oxygen Reduction Reaction

Transition metal single-atom catalysts (SACs) are currently a hot area of research in the field of electrocatalytic oxygen reduction reaction (ORR). In this review, the recent advances in transition metal single-atom supported by 2D materials as catalysts for ORR with high performance are reported. Due to their large surface area, uniformly exposed lattice plane, and adjustable electronic state, 2D materials are ideal supporting materials for exploring ORR active sites and surface reactions. The rational design principles and synthetic strategies of transition metal SACs supported by 2D materials are systematically introduced while the identification of active sites, their possible catalytic mechanisms as well as the perspectives on the future of transition metal SACs supported by 2D materials for ORR applications are discussed. Finally, according to the current development trend of ORR catalysts, the future opportunities and challenges of transition metal SACs supported by 2D materials are summarized.     

Acidic hydrolysis of a poly(vinyl acetate) matrix by the catalytic effect of Ag nanoparticles and the micellization of Ag‐metal‐containing polymer

In this study, we conveniently obtained Ag(0)–polymer nanocomposites by reacting AgNO₃ with commercial poly(vinyl acetate) (PVAc) in the absence of a special reducing agent. The formation of Ag(0) metal was detected after formic acid (HCOOH) was added to a PVAc–AgNO₃ complex system, and some of the acetate groups of the PVAc backbone were hydrolyzed to form hydroxyl groups (OH) under the catalytic effect of the reduced Ag(O) metal. Here, the structure of the partially hydrolyzed PVAc backbone was represented as PVOH‐PVAc. X‐ray diffraction spectra showed that the Ag(0) metal generated in this method was in the form of Ag crystals. The structure of the Ag(0)–polymer was analyzed by ¹H‐NMR and ¹³C‐NMR spectroscopy. The micellization of the Ag(0)–polymer was also investigated by the addition of an inducing solvent to the formic acid solution of Ag(0)–polymer. The image showed that the morphology of the Ag micelles in the H₂O‐induced solvent was a Ag corona with a Ag shell, and that in the p‐xylene induced solvent showed a Ag cluster core structure. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1457–1464, 2006     

Thermo-mechanical analysis of 3D manufactured electrodes for solid oxide fuel cells

Additive manufacturing has widened the scope for designing more performing microstructures for solid oxide fuel cells (SOFCs). Structural modifications, such as the insertion of ceramic pillars within the electrode, facilitate ion transport and boost the electrochemical performance. However, questions still remain on the related mechanical requirements during operation. This study presents a comprehensive thermal-electrochemical-mechanical model targeted to assess the stress distribution in 3D manufactured electrodes. Simulations show that a dense pillar increases the stress distribution by ca. 10 % compared to a flat electrode benchmark. The stress is generated by the material thermal contraction and intensifies at the pillar-electrolyte junction while external loads have negligible effects. An analysis on manufacturing inaccuracies indicates that sharp edges, surface roughness and tilted pillars intensify the stress; nonetheless, the corresponding stress increase is narrow, suggesting that manufacturing inaccuracies can be easily tolerated. The model points towards robust design criteria for 3D manufactured electrodes.     

Rational Design on Wrinkle-Less Transfer of Transition Metal Dichalcogenide Monolayer by Adjustable Wettability-Assisted Transfer Method

Transfer-induced wrinkles are universal issues when transferring transition metal dichalcogenide (TMDC) monolayer from an as-grown substrate to a target substrate. The undesired transfer-induced wrinkles can mainly be attributed to wettability, which refers to the ability of a liquid to come in contact with a solid surface. Herein, an adjustable wettability-assisted transfer (AWAT) method with different mixtures of transfer media to reduce the density of wrinkles is developed. By manipulating the wettability of the transfer medium with different ratios of alcohol and de-ionized (DI) water, the TMDC monolayer is smoothly attached to the target substrate, thus achieving a wrinkle-less transferred TMDC monolayer. With this method, the density of wrinkles can be decreased by ≈ 15–20% compared with the conventional transfer method by pure DI water. The transferred MoS₂ monolayer with the AWAT method can achieve enhanced carrier mobility from ≈ 20 to ≈ 35 cm² V⁻¹ s⁻¹ in average, which is 30 times larger than that transferred by pure DI water. The AWAT method applied to a WS₂ monolayer onto a SiO₂/p⁺-Si substrate and a MoS₂ monolayer onto a HfO₂/p⁺-Si substrate are demonstrated, which is beneficial in research and applications involving the transfer of TMDC monolayer.     

Infrared proximity sensor using organic light-emitting diode with quantum dots converter

An efficient visible-to-infrared conversion film is made by blending CdTe quantum dots (CdTe QDs) of 12 nm diameter in a polyvinylpyrrolidone 360 (PVP 360) polymer matrix cast by water solution. The solid-state photoluminescence quantum efficiency exceeds 10% with emission peak at 810 nm. Strong 810 emission is obtained by combining the quantum dot film and a green polyfluorene light-emitting diode. Color filter is used to remove residual light below 780 nm to make it entirely invisible. Infrared photo-detector is made by blending poly[5-(5-(2,5-bis(decyloxy)-4-methylphenyl)thiophen-2-yl)-2,3-bis(4-(2-ethylhexyloxy)phenyl)-7-(5-methylthiophen-2-yl)thieno[3,4-b]pyrazine] (PBDOTTP) with band-gap 1.2 eV and (6,6)-phenyl-C61-butyric acid methyl ester (PCBM). The pixel contains one PD surrounded by four PLED on its four sides. The active areas of the five devices are all 1 cm by 1 cm and they are on the same plane. Infrared proximity sensor with photo-current over 300 nA at 10 cm object distance is achieved by detecting the reflected infrared signal.     

Efficient doping and energy transfer from ZnO to Eu3+ ions in Eu(3+)-doped ZnO nanocrystals

Successful doping of Eu3+ ions into ZnO nanocrystals has been realized by using a low temperature wet chemical doping technique. The substitution of Eu3+ for Zn2+ is shown to be dominant in the Eu-doped ZnO nanocrystals by analyzing the X-ray diffraction patterns, transmission electron microscopy images, Raman and selectively excited photoluminescence spectra. Measurement of the luminescence from the samples shows that the excited ZnO transfers the excited energy efficiently to the doped Eu3+ ions, giving rise to efficient emission at red spectral region. The red emission quantum yield is measured to be 31% at room temperature. The temperature dependence of photoluminescence and the photoluminescence excitation spectra have also been investigated, showing strong energy coupling between the ZnO host and Eu3+ ions through free and bound excitons. The result indicates that Eu3+ ion-doped ZnO nanocrystals are promising light-conversion materials and have potential application in highly distinguishable emissive flat panel display and LED backlights.