Novia Amalia Sholeha
College of Vocational Studies, Bogor Agricultural University (IPB University), Bogor 16151, Indonesia

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UiO-66-based Photocatalysts for CO2 to Methanol Conversion Potential: Mechanisms and Performance Benchmarks Septian Wahyu Setiawan; Ummi Aminatus Sa'diyah; Silvana Dwi Nurherdiana; Novia Amalia Sholeha; Hamzah Fansuri; Djoko Hartanto
AJARCDE (Asian Journal of Applied Research for Community Development and Empowerment) Vol. 10 No. 1 (2026)
Publisher : Asia Pacific Network for Sustainable Agriculture, Food and Energy (SAFE-Network)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.29165/ajarcde.v10i1.929

Abstract

The increasing concentration of carbon dioxide (CO2) emissions has driven the development of technologies for converting CO2 into environmentally friendly fuels through photocatalytic reduction. One of the widely studied materials is UiO-66, a metal–organic framework (MOF)-based photocatalyst. This article presents a literature review aimed at analyzing recent research developments on the application of UiO-66 for CO2 reduction. Relevant studies were systematically collected from Scopus, ScienceDirect, and Google Scholar databases within the 2015–2025 period, focusing on experimental investigations and material modifications. The synthesis of the reviewed studies indicates that the photocatalytic performance of UiO-66 is influenced by metal modification, functional group incorporation, band gap engineering, and the use of co-catalysts. These strategies enhance visible light absorption and improve the effectiveness of light energy utilization, thereby promoting CO2 reduction activity. Although UiO-66 demonstrates promising potential, improvements in material stability and reaction performance consistency remain necessary for large-scale industrial applications. Contribution to Sustainable Development Goals (SDGs):SSDG 7: Affordable and Clean EnergySDG 9: Industry, Innovation, and InfrastructureSDG 12: Responsible Consumption and ProductionSDG 13: Climate Action
Surface Chemistry and Adsorption Behavior of Methylene Blue on Functionalized Carbon Materials: A Comprehensive Study Maria Ulfa; Rizki Fauzia Hanif; Novia Amalia Sholeha
Communications in Science and Technology Vol 10 No 2 (2025)
Publisher : Komunitas Ilmuwan dan Profesional Muslim Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21924/cst.10.2.2025.1711

Abstract

The increasing release of synthetic dyes, particularly methylene blue (MB), from textile effluents has become a major environmental andhealth concern, highlighting the urgent need for efficient remediation strategies. Adsorption remains one of the most effective techniques for dye removal due to its simplicity, low cost, and high efficiency. This review discusses the surface chemistry and adsorption behavior of MB on functionalized carbon-based materials, emphasizing how physicochemical characteristics, surface modifications, and functional groups influence adsorption capacity and selectivity. Recent progress in developing engineered carbonaceous adsorbents—such as activated carbon (AC), graphene derivatives, carbon nanotubes, and hybrid carbon composites—has significantly improved the removal performance of MB through enhanced structural and chemical interactions. The ACHC-KOM-1 carbon composite, for instance, exhibits remarkable photocatalytic-assisted adsorption, achieving complete MB degradation under optimized conditions. Surface functional groups and pore architecture are decisive factors governing adsorption efficiency. Oxygen-containing moieties, including carboxyl (–COOH) and hydroxyl (–OH), create active sites that facilitate electrostatic attraction and hydrogen bonding with cationic MB molecules. Nitrogen functionalities (–N), introduced via heteroatom doping, enhance electron-donating properties and π–π interactions between MB aromatic rings and the conjugated carbon framework, thereby strengthening molecular affinity. Pore dimensions further regulate accessibility and diffusion, with micropores (<2 nm) providing strong confinement and high adsorption energy, while mesopores (2–50 nm) promote rapid diffusion and prevent pore blockage. The synergistic combination of abundant surface functionalities and hierarchical porosity governs the overall adsorption capacity, kinetics, stability, and regeneration potential of carbon-based adsorbents for dye removal. The mechanistic framework presented here distinguishes biomass-derived and non-biomass carbon adsorbents, enabling rational design of high-performance materials. These findings offer practical optimization guidelines for industrial-scale methylene blue removal while supporting sustainable, circular-economy-aligned water purification technologies.