RESUMO
Transition metal dichalcogenides (TMDs) have attracted great interest owing to their fascinating properties with atomically thin nature. Although TMDs have been exploited for diverse applications, the effective role of TMDs in the synthesis of metal nanowires has not been explored. Here, we propose a new approach to synthesize ultrathin metal nanowires using TMDs for the first time. High-quality ultrathin nanowires with an average diameter of 11.3 nm are successfully synthesized for realizing high-performance transparent conductors that exhibit excellent conductivity and transparency with low haze. The growth mechanism is carefully investigated using high-resolution transmission electron microscopy, and growth of nanowires with tunable diameters is achieved by controlling the nanosheet dimension. Finally, we unravel the important role of TMDs acting as both reducing and nucleating agents. Therefore, our work provides a new strategy of the TMD as an innovative material for the growth of metal nanowires as a promising building block in next-generation optoelectronics.
RESUMO
Reducing the diameter of silver nanowires has been proven to be an effective way to improve their optoelectronic performance by lessening light attenuation. The state-of-the-art silver nanowires are typically around 20 nm in diameter. Herein we report a modified polyol synthesis of silver nanowires with average diameters as thin as 13 nm and aspect ratios up to 3000. The success of this synthesis is based on the employment of benzoin-derived radicals in the polyol approach and does not require high-pressure conditions. The strong reducing power of radicals allows the reduction of silver precursors to occur at relatively low temperatures, wherein the lateral growth of silver nanowires is restrained because of efficient surface passivation. The optoelectronic performance of as-prepared 13 nm silver nanowires presents a sheet resistance of 28 Ω sq-1 at a transmittance of 95% with a haze factor of â¼1.2%, comparable to that of commercial indium tin oxide (ITO).
RESUMO
While tremendous efforts have been dedicated to developing cellulose-based ultraviolet (UV)-blocking films, challenges still remain in simultaneously achieving high transparency, low haze and excellent UV shielding properties via simple and green strategy. Here, we present a facile and eco-friendly route to fabricate flexible, biodegradable and clear UV-shielding nano-MIL-88A(Fe)@carboxymethylated cellulose films (M(Fe)CCFs) via in situ synthesis of nano-MIL-88A(Fe) in carboxymethylated cellulose hydrogel followed by natural drying. The carboxymethylated cellulose film has high transmittance (93.2%) and low haze (1.8%). The introduction of nano-MIL-88A(Fe) endowed M(Fe)CCFs superior UV-shielding ability, while retaining high transmittance (81.5-85.3%) and low haze (2.5-4.9%). Moreover, M(Fe)CCFs showed stable UV blocking performance under UV irradiation, high temperature, acidic or alkaline conditions. Quite encouragingly, the UV-shielding ability of M(Fe)CCFs did not deteriorate, even after 30 days of immersion in aqueous solution, providing films with a long-term use capacity. Thus, M(Fe)CCFs show high potential in the UV protection field. Overall, these UV-blocking films with outstanding performances are a promising candidate to replace conventional film materials made from synthetic polymers in fields such as packaging and flexible electronics.
RESUMO
We report the fabrication of stretchable transparent electrode films (STEF) using 15-nm-diameter Ag nanowires networks embedded into a cross-linked polydimethylsiloxane elastomer. 15-nm-diameter Ag NWs with a high aspect ratio (Ë1000) were synthesized through pressure-induced polyol synthesis in the presence of AgCl particles with KBr. These Ag NW network-based STEF exhibited considerably low haze values (<1.5%) with a transparency of 90% despite the low sheet resistance of 20 Ω/sq. The STEF exhibited an outstanding mechanical elasticity of up to 20% and no visible change occurred in the sheet resistance after 100 cycles at a stretching-release test of 20%.
RESUMO
The transparent flexible supercapacitor is considered to be the key energy-storage component for the development of wearable and fully transparent electronic devices. However, the current transparent supercapacitor faces the low-haze challenge, which is essential for the high-definition visualization in transparent electronics. Herein, we developed a facile interfacial polymerization approach for the large-area preparation of flexible polypyrrole/polyethylene terephthalate (PPy/PET) transparent conductive films in a cost-effective way. The PPy/PET film exhibits a highly uniform morphology and a low haze level of 1.40% (corresponding to high definition) as well as negligible resistance changing under an ultrasmall bending radius. The sandwich-structured, large-area, transparent supercapacitor assembled based on the PPy/PET films also keeps a similar low haze level. A facile N, N-dimethylformamide etchant-written strategy on the PPy/PET film is developed to fabricate the patterned micro-supercapacitors (MSCs) in series in scalable area, which show a low haze level of 1.66% and a high transparency of 70.2%. Significantly, the low-haze MSC possesses high energy-storage capacity and presents almost no capacitance loss at an extreme bending state. This work demonstrates a facile preparation of large-area and low-haze transparent flexible supercapacitors and also enlightens broad interests in their potential integrity toward the fully transparent wearable electronics.
RESUMO
Copper nanowire (Cu NW) based transparent conductors are promising candidates to replace ITO (indium-tin-oxide) owing to the high electrical conductivity and low-cost of copper. However, the relatively low performance and poor stability of Cu NWs under ambient conditions limit the practical application of these devices. Here, we report a solution-based approach to wrap graphene oxide (GO) nanosheets on the surface of ultrathin copper nanowires. By mild thermal annealing, GO can be reduced and high quality Cu r-GO core-shell NWs can be obtained. High performance transparent conducting films were fabricated with these ultrathin core-shell nanowires and excellent optical and electric performance was achieved. The core-shell NW structure enables the production of highly stable conducting films (over 200 days stored in air), which have comparable performance to ITO and silver NW thin films (sheet resistance â¼28 Ω/sq, haze â¼2% at transmittance of â¼90%).