As promising candidates in the field of artificial muscles, ionic‐polymer–metal composites (IPMCs) still cannot simultaneously provide large deformations and fast responses, which has limited their practical applications. In this study, to overcome this issue, a Nafion‐based IPMC with high‐quality metal electrodes is fabricated via novel isopropanol‐assisted electroless plating. The IPMC exhibits a large tip displacement (35.3 mm, 102.3°) under a low direct‐current driving voltage and ultrafast response (>10 Hz) under an alternating‐current (AC) voltage. Furthermore, the simultaneous integration of a large deformation and fast response can be achieved by the IPMC under a high‐frequency (19 Hz) AC voltage, where the largest bending amplitude is 5.9 mm and the highest bending speed reaches 224.2 mm s−1 (596.2° s−1). Additionally, the lightweight IPMC exhibits a decent load capacity and can lift objects 20 times heavier. The outstanding performances of the Nafion IPMC are demonstrated by mimicking biological motions such as petal opening/closing, tendril coiling/uncoiling, and high‐frequency wing flapping. This study paves the way for the fabrication of lightweight actuators with simultaneous large displacements and fast responses for promising applications in biomedical devices and bioinspired robotics.
Organic molecular aggregates have attracted widespread attention over the past decade owing to their unique optoelectronic properties in the aggregate state, which mainly involves the effects of aggregation structure as well as molecular packing mode. Although many examples of H‐ and J‐aggregates defined by molecular exciton model have been found, there are also other types of unconventional aggregates, especially for aggregation‐induced emission (AIE) system. In this review, the recent progress of some examples of basic and novel aggregate forms, as well as coassembled forms, presenting distinctive optical features, such as optical waveguide and polarization emission, polymorph‐dependent emission and stimuli‐responsive luminescence are presented. The systematic insight into the relationship between the aggregation structure and emission property is discussed. Guidelines are therefore anticipated and will direct the future preprogramming molecular design so as to fine‐tune the emission feature through a specific aggregation model for developing organic molecular aggregates with desirable optoelectronic properties.
The development of organic fluorophores with efficient solid-state emissions or aggregated-state emissions in the red to near-infrared region is still challenging. Reported herein are fluorophores having aggregation-induced emission ranging from the orange to far red/near-infrared (FR/NIR) region. The bioimaging performance of the designed fluorophore is shown to have potential as FR/NIR fluorescent probes for biological applications.
Cross dipole stacking based on a novel fluorescent molecule, 9,10-bis (2,2-diphenylvinyl) anthracene (BDPVA), is presented. The butterfly-like structure of BDPVA is the key feature to form the unique aggregation structure and such a stacking mode is highly beneficial for fluorescence emission, resulting in high-performance amplified spontaneous emission and electroluminescence of BDPVA.
Here, we design and
synthesize an organic laser molecule, 2,7-diphenyl-9H-fluorene (LD-1), which has state-of-the-art integrated
optoelectronic properties with a high mobility of 0.25 cm2 V–1 s–1, a high photoluminescence
quantum yield of 60.3%, and superior deep-blue laser characteristics
(low threshold of P
th = 71 μJ cm–2 and P
th = 53 μJ
cm–2 and high quality factor (Q) of ∼3100 and ∼2700 at emission peaks of 390 and 410
nm, respectively). Organic light-emitting transistors based on LD-1
are for the first time demonstrated with obvious electroluminescent
emission and gate tunable features. This work opens the door for a
new class of organic semiconductor laser molecules and is critical
for deep-blue optical and laser applications.
Insights into the origin of the fluorescence responsive to protonation-deprotonation stimuli were provided through the study on the crystals of a new stimuli-responsive molecule BP3VA. And the transformation between microcrystals demonstrated the varying emissions of the BP3VA powder.
Two tetraphenylethene (TPE)-functionalized spiropyran (SP) molecules with very similar structure were designed and synthesized. The two molecules exhibit aggregation-induced emission (AIE) properties, as well as multistimuli-responsive color-changing properties, such as photochromism and acidchromism. The investigation of their different photochromic and acidchromic characteristics and dual-response fluorescent switch during isomerization indicated that the different link position between TPE and SP will significantly affect the extended π-conjugated system, resulting in completely different photochromic and acidchromic properties.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.