An evaluation framework for low performers and human resource management planning: Application to a life insurance company in Korea.

This study comprehensively explores the factors that lead to low performers in an organization. A thorough literature review was conducted to construct an interview guide and obtain classification criteria for the factors that lead to low performers. Managers and low performers at multiple firms were interviewed individually to understand the various phenomena related to low performers in organizations. Based on the content of these interviews, 12 factors, classified into individual, leader, work, and organizational dimensions, were identified after three rounds of revisions by business administration experts. Next, a case study of Korea's S Life Insurance Company was conducted to examine the practical implications of the factors that contribute to creating low performers. In this case study, the analytic hierarchy process (AHP), involving eight departmental heads S Life Insurance Company's HR division, was utilized to identify the main factors that must be considered when evaluating low performers. While previous studies have examined low performers either at the individual, organizational, or institutional levels, this study presents a comprehensive and integrated evaluation framework of the factors that cause low performers. The proposed framework facilitates the identification and evaluation of low performers in various organizations and industries, and thus has practical implications in terms of establishing strategies to manage low performers more efficiently and improve organizational performance.

Dielectric Elastomers UV-Cured from Poly(dimethylsiloxane) Solution in Vinyl Acetate.

Poly(dimethylsiloxane) (PDMS) has been extensively used as an electroactive polymer material because it exhibits not only excellent moldability but also mechanical properties sufficient enough for electroactive performance despite low dielectric permittivity. Its low dielectric property is due to its molecular non-polarity. Here, we introduce a polar group into a PDMS elastomer by using vinyl acetate (VAc) as a crosslinker to improve the dielectric permittivity. We synthesized a high-molecular weight PDMS copolymer containing vinyl groups, namely poly(dimethylsiloxane-co-methylvinylsiloxane) (VPDMS), and prepared several of the VPDMS solutions in VAc. We obtained transparent PDMS films by UV curing of the solution layers. Electromechanical actuation-related physical properties of one of the UV-cured films were almost equivalent to or superior to those of platinum-catalyzed hydrosilylation-cured PDMS films. In addition, saponification of the UV-cured film significantly improved the electrical and mechanical properties (ɛ' ~ 44.1 pF/m at 10 kHz, E ~ 350 kPa, ɛ ~ 320%). The chemical introduction of VAc into PDMS main chains followed by saponification would offer an efficacious method of enhancing the electroactive properties of PDMS elastomers.

Monolithic focus-tunable lens technology enabled by disk-type dielectric-elastomer actuators.

We propose a monolithic focus-tunable lens structure based on the dielectric-elastomer actuator (DEA) technology. In our focus-tunable lens, a soft lens and radial in-plane actuator mimicking the ocular focal-tuning mechanism are constructed in a single body of an optimized dielectric-elastomer film. We provide device fabrication methods including elastomer synthesis, structure formation, and packaging process steps. Performance test measurements show 93% focal tunability and 7 ms response time under static and dynamic electrical driving conditions, respectively. These performance characteristics are substantially enhanced from the previous polylithic DEA tunable lens by a factor 1.4 for the focal tunability and a factor 9.4 for the dynamic tuning-speed limit. Therefore, we obtain greatly enhanced focal tuning control in a remarkably simple and compact device structure.

Facile Functionalization of Poly(Dimethylsiloxane) Elastomer by Varying Content of Hydridosilyl Groups in a Crosslinker.

Crosslinked poly(dimethylsiloxane) (PDMS) has been widely used as a dielectric elastomer for electrically driven actuators because it exhibits high elasticity, low initial modulus, and excellent moldability in spite of low dielectric constant. However, further improvement in the characteristics of the PDMS elastomer is not easy due to its chemical non-reactivity. Here, we report a simple method for functionalizing the elastomer by varying content of hydridosilyl groups in PDMS acted as a crosslinker. We synthesized poly(dimethylsiloxane-co-methylvinylsiloxane) (VPDMS) and poly(dimethylsiloxane-co-methylsiloxane) (HPDMS). Tri(ethylene glycol) divinyl ether (TEGDE) as a polar molecule was added to the mixture of VPDMS and HPDMS. TEGDE was reacted to the hydridosilyl group in HPDMS during crosslinking between VPDMS and HPDMS in the presence of platinum as a catalyst. Permittivity of the crosslinked film increased from ca. 25 to 36 pF/m at 10 kHz without a decline in other physical properties such as transparency and elasticity (T > 85%, E ~150 kPa, ɛ ~270%). It depends on the hydridosilyl group content of HPDMS. The chemical introduction of a new molecule into the hydridosilyl group in HPDMS during crosslinking would provide a facile, effective method of modifying the PDMS elastomers.

Elastomer thin-film pressure sensor based on embedded photonic tunnel-junction arrays.

We propose an elastomer thin-film pressure sensor enabled by pressure-sensitive optical signals through vertical photonic tunnel-junction couplers. We provide the operation principle, design, fabrication, and test results from a 50 µm thick polydimethylsiloxane sheet accommodating embedded vertical photonic tunnel-junction couplers. The result with a 5 mm long device shows a differential optical power change that is ∼140% of the incident power under moderate external pressure of ∼40 kPa, thereby clearly demonstrating a robust pressure-sensing capability realized in a highly flexible, lightweight, transferrable, optically transparent, and bio-compatible thin-film material. Therefore, the proposed approach potentially enables versatile pressure and touch sensors for many applications in practice.

Electro-Active Polymer Based Soft Tactile Interface for Wearable Devices.

This paper reports soft actuator based tactile stimulation interfaces applicable to wearable devices. The soft actuator is prepared by multi-layered accumulation of thin electro-active polymer (EAP) films. The multi-layered actuator is designed to produce electrically-induced convex protrusive deformation, which can be dynamically programmable for wide range of tactile stimuli. The maximum vertical protrusion is and the output force is up to 255 mN. The soft actuators are embedded into the fingertip part of a glove and front part of a forearm band, respectively. We have conducted two kinds of experiments with 15 subjects. Perceived magnitudes of actuator's protrusion and vibrotactile intensity were measured with frequency of 1 Hz and 191 Hz, respectively. Analysis of the user tests shows participants perceive variation of protrusion height at the finger pad and modulation of vibration intensity through the proposed soft actuator based tactile interface.

Flexible transparent displays based on core/shell upconversion nanophosphor-incorporated polymer waveguides.

Core/shell (C/S)-structured upconversion nanophosphor (UCNP)-incorporated polymer waveguide-based flexible transparent displays are demonstrated. Bright green- and blue-emitting Li(Gd,Y)F4:Yb,Er and Li(Gd,Y)F4:Yb,Tm UCNPs are synthesized via solution chemical route. Their upconversion luminescence (UCL) intensities are enhanced by the formation of C/S structure with LiYF4 shell. The Li(Gd,Y)F4:Yb,Er/LiYF4 and Li(Gd,Y)F4:Yb,Tm/LiYF4 C/S UCNPs exhibit 3.3 and 2.0 times higher UCL intensities than core counterparts, respectively. In addition, NaGdF4:Yb,Tm/NaGdF4:Eu C/S UCNPs are synthesized and they show red emission via energy transfer and migration of Yb3+ → Tm3+ → Gd3+ → Eu3+. The C/S UCNPs are incorporated into bisphenol A ethoxylate diacrylate which is used as a core material of polymer waveguides. The fabricated stripe-type polymer waveguides are highly flexible and transparent (transmittance > 90% in spectral range of 443-900 nm). The polymer waveguides exhibit bright blue, green, and red luminescence, depending on the incorporated UCNPs into the polymer core, under coupling with a near infrared (NIR) laser. Moreover, patterned polymer waveguide-based display devices are fabricated by reactive ion etching process and they realize bright blue-, green-, and red-colored characters under coupling with an NIR laser.

Thin film display based on polymer waveguides.

This paper reports thin, transparent, and soft displays based on polymer waveguides that are compliant with curvilinear interfaces. In order to prove a feasibility of optical waveguide for a flexible display, we suggest the waveguide fabricated by a multi-step lithography process using two photo-curable pre-polymers with different refractive index. The displays are composed of light sources, polymer waveguides, and scatter patterns. The light signal propagating through the waveguides forms images of the scatter patterns by deflecting the light signals to outer surface. The scatter patterns are configured to a seven-segment. The seven-segment design with a switching methodology of the light sources contributes to selectively representing all decimal numbers from 0 to 9 by combination of activated segments. For a large area display based on the proposed methodology, a single light source interconnected to multi-waveguide section is integrated with a QWERTY key pad design. The display shows high transparency and flexibility without visual distortion.

1.6-micrometer emission from Ho3+-doped fluoride glasses.

We have investigated the spectroscopic properties of the 1.6-micrometer emission from the 5I(5) --> 5I(7) transition of Ho3+ ions in fluoride glasses for use in U-band fiber amplifiers. The intensity profile of the emission peaks at approximately 1660 nm, with a full width at half-maximum of approximately 60 nm. The measured lifetime and emission cross section are approximately 230 micros and approximately 5.4 x 10(-21) cm2, respectively. Frequency upconversion to the 5F(1) state occurs simultaneously with excitation of the 1.6-micrometer emission, so the shorter-wavelength side of the 5I(8) --> 5I(5) absorption spectrum is favorable for population of the 5I(5) state. Codoping with rare earths such as Tb3+, Dy3+, Eu3+, and Nd3+ decreases the lifetimes of the lower-lying 5I(6) and 5I(7) levels and as a result would be of benefit in achieving population inversion between the fluorescing level and the lower-lying levels.