황동목 교수
Dong-Mok Hwang
성균관대학교 신소재공학과 · 재료과학
연구실 소개
황동목 교수의 연구실은 2차원 물질 기반의 나노전자소자 및 에너지 장치의 핵심 도전 과제인 인터페이스 제어와 소자 성능 향상을 목표로 합니다. 특히 모재스티드(MoS₂), 그래핀, 스테이션러리 산화물 등 다양한 2차원 반도체 및 나노소재를 활용해 고성능 전자소자, 초민감도 pH 센서, 안정적인 리이on 이온 배터리 등 응용 기술을 개발하고 있습니다. 솔루션 기반 공정, 원자적 깨끗한 인터페이스 형성, 그리고 스케일업 가능한 전이 공정 기술을 접목한 실용화 기반 연구가 특징입니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Two-dimensional transition metal dichalcogenides (TMDCs) have emerged as promising materials for next-generation electronics due to their excellent semiconducting properties. However, high contact resistance at the metal-TMDC interface plagues the realization of high-performance devices. Here, an effective metal-interlayer-semiconductor (MIS) contact is demonstrated, wherein an ultrathin ZnO interlayer is inserted between the metal electrode and MoS<sub>2</sub>, providing damage-free and clean i
The conventional pH sensor based on the graphene ion-sensitive field-effect transistor (Gr-ISFET), which operates with an electrostatic gating at the solution-graphene interface, cannot have a pH sensitivity above the Nernst limit (∼59 mV/pH). However, for accurate detection of the pH levels of an aqueous solution, an ultrasensitive pH sensor that can exceed the theoretical limit is required. In this study, a novel Gr-ISFET-based pH sensor is fabricated using proton-permeable defect-engineered g
We investigate the electric transport in a graphene-organic dye hybrid and the formation of p-n junctions. In the conventional approach, graphene p-n junctions are produced by using multiple electrostatic gates or local chemical doping, which produce different types of carriers in graphene. Instead of using multiple gates or typical chemical doping, a different approach to fabricate p-n junctions is proposed. The approach is based on optical gating of photosensitive dye molecules; this method ca
Molybdenum disulfide (MoS<sub>2</sub>) presents fascinating properties for next-generation applications in diverse fields. However, fully exploiting the best properties of MoS<sub>2</sub> in largescale practical applications still remains a challenge due to lack of proper processing methods. Solution-based processing can be a promising route for scalable production of MoS<sub>2</sub> nanosheets, but the resulting assembled film possesses an enormous number of interfaces that significantly compro
Sn-based materials have been highlighted as promising anodes for next-generation batteries; however, such alloying-based anodes suffer from gradual cell degradation caused by the associated large volume changes, leading to particle pulverization and an unstable solid electrolyte interphase (SEI). A key to constructing a stable SEI as well as effectively buffering the large volume expansion is to establish appropriate electrolyte conditions. In this work, to induce the formation of a favorable SE
The synthesis of uniform low-defect graphene on a catalytic metal substrate is getting closer to the industrial level. However, its practical application is still challenging due to the lack of an appropriate method for its scalable damage-free transfer to a device substrate. Here, an efficient approach for a defect-free, etchant-free, wrinkle-free, and large-area graphene transfer is demonstrated by exploiting a multifunctional viscoelastic polymer gel as a simultaneous shock-free adhesive and
In this work, we developed an atomically thin (∼2.5 nm) heterostructure consisting of a monolayer rhodamine 6G (R6G) film as a photoactive layer that was sandwiched between graphene films functioning as channels (graphene-R6G-graphene, G-R-G). Through a comparison of results of both photocurrent measurements and chemically enhanced Raman scattering (CERS) experiments, we found that our G-R-G heterostructure exhibited ∼7 and ∼30 times better performance than R6G-attached single-graphene (R6G-grap
In MoS<sub>2</sub>-carbon composite catalysts for hydrogen evolution reaction (HER), the carbon materials generally act as supports to enhance the catalytic activity of MoS<sub>2</sub> nanosheets. The carbon support provides a large surface area for increasing the MoS<sub>2</sub> edge site density, and its physical structure can affect the electron transport rate in the composite catalysts. However, despite the importance of the carbon materials, direct observation of the effects of the physical
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