성균관대학교 · Energy
Xinghui Liu 교수의 연구실은 에너지 전환과 환경 정화를 위한 고성능 나노촉매 기반 기술 개발에 초점을 맞추고 있습니다. 특히 산성 조건에서의 산화 반응(OER)과 수소 발생 반응(HER)에서 뛰어난 안정성과 활성도를 보이는 단일 원자 촉매(SAC) 및 나노구조 헤테로구조를 설계하고, 전자적 특성과 반응 메커니즘을 이론적·실험적 융합으로 규명합니다. 또한 전기화학적 반응에서의 활성 부위 규명과 재료의 동적 재구성 메커니즘을 분석함으로써 지속 가능한 청정 기술의 실현 가능성을 탐색하고 있습니다.
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The poor catalyst stability in acidic oxidation evolution reaction (OER) has been a long-time issue. Herein, we introduce electron-deficient metal on semiconducting metal oxides-consisting of Ir (Rh, Au, Ru)-MoO<sub>3</sub> embedded by graphitic carbon layers (IMO) using an electrospinning method. We systematically investigate IMO's structure, electron transfer behaviors, and OER catalytic performance by combining experimental and theoretical studies. Remarkably, IMO with an electron-deficient m
Abstract Single‐atom catalysts (SACs) have become the forefront of energy conversion studies, but unfortunately, the origin of their activity and the interpretation of the synchrotron spectrograms of these materials remain ambiguous. Here, systematic density functional theory computations reveal that the edge sites—zigzag and armchair—are responsible for the activity of the graphene‐based Co (cobalt) SACs toward hydrogen evolution reaction (HER). Then, edge‐rich (E)‐Co single atoms (SAs) were ra
Although single-atom catalysts (SACs) have been at the vanguard of energy conversion research, the selection of suitable substrates and single-atom specification permits remains ambiguous. Herein, we fabricated Co-g-C3N4/rGO SACs (Co-CNG) by coupling the suitable single-atom Co with a promising substrate of g-C3N4/rGO. Remarkably, Co-CNG exhibits even comparable HER performance (10 mA cm–2 at ∼47 mV) with commercially available Pt/C (10 mA cm–2 at ∼48 mV) and outperformed non-noble transition-me
Direct electrochemical nitrate reduction reaction (NITRR) is a promising strategy to alleviate the unbalanced nitrogen cycle while achieving the electrosynthesis of ammonia. However, the restructuration of the high-activity Cu-based electrocatalysts in the NITRR process has hindered the identification of dynamical active sites and in-depth investigation of the catalytic mechanism. Herein, Cu species (single-atom, clusters, and nanoparticles) with tunable loading supported on N-doped TiO<sub>2</s
Devising a desirable nano-heterostructured photoelectrode based on the charge transfer kinetics mechanism is a pivotal strategy for implementing efficient photoelectrocatalytic (PEC) technology, since the charge separation and utilization efficiency of a photoelectrode is critical to its PEC performance. Herein, we fabricate a F-Co3O4@Bi2WO6 core–shell hetero-array photoanode by coupling Bi2WO6 nanosheets with F-Co3O4 nanowires using a simple solvothermal solution method. The three-dimensional h
• Advancements in environmental cleanup use nanotech for efficient pollutant removal. • Electrochemical methods and sorption tech offer effective pollutant removal. • Hybrid treatment systems with multiple approaches for synergistic pollutant removal. • Green remediation prioritizes sustainability in cleanup efforts. Recent advancements in environmental remediation have significantly improved the treatment of soil and water pollution, yet the complexity and dispersion of emerging pollutants rema
Large arrays of 3-terminal nanoelectromechanical graphene switches are fabricated. The switch is designed with a novel geometry that leads to low actuation voltages and improved mechanical integrity, while reducing adhesion forces, which improves the reliability of the switch. A finite element model including non-linear electromechanics is used to simulate the switching behavior and to deduce a scaling relation between the switching voltage and device dimensions.
Finding effective strategies to design efficient photocatalysts and decompose refractory organic compounds in wastewater is a challenging problem. Herein, by coupling element doping and constructing heterostructures, S-scheme CdS QDs/La-Bi<sub>2</sub>WO<sub>6</sub> (CS/LBWO) photocatalysts are designed and synthesized by a simple hydrothermal method. As a result, the RhB degradation efficiency of the optimized 5% CS/LBWO reached 99% within 70 min of illumination with excellent stability and recy
Abstract Due to γ‐Bi 2 MoO 6 (BMO) has attracted considerable attention because of its unique layered perovskite structure and excellent electrical conductivity. However, the easy recombination of electron–hole pairs limits its practical application. To address this issue, we successfully prepared aliovalent Cd 2+ doped BMO (Cd‐BMO) by using a simple hydrothermal method for the degradation of the sulfamethoxazole (SMZ) and Rhodamine B (RhB). The result found that the degradation efficiency of Cd