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International Journal of Renewable Energy Development
Published by Center of Biomass and Renewable Energy
ISSN : 22524940     EISSN : 27164519     DOI : https://doi.org/10.61435/ijred.xxx.xxx
Core Subject : Science, Engineering,
Control & Systems Engineering Earth & Planetary Sciences Electrical & Electronics Engineering Energy Engineering
The International Journal of Renewable Energy Development - (Int. J. Renew. Energy Dev.; p-ISSN: 2252-4940; e-ISSN:2716-4519) is an open access and peer-reviewed journal co-published by Center of Biomass and Renewable Energy (CBIORE) that aims to promote renewable energy researches and developments, and it provides a link between scientists, engineers, economist, societies and other practitioners. International Journal of Renewable Energy Development is currently being indexed in Scopus database and has a listing and ranking in the SJR (SCImago Journal and Country Rank), ESCI (Clarivate Analytics), CNKI Scholar as well as accredited in SINTA 1 (First grade category journal) by The Directorate General of Higher Education, The Ministry of Education, Culture, Research and Technology, The Republic of Indonesia under a decree No 200/M/KPT/2020. The scope of journal encompasses: Photovoltaic technology, Solar thermal applications, Biomass and Bioenergy, Wind energy technology, Material science and technology, Low energy architecture, Geothermal energy, Wave and tidal energy, Hydro power, Hydrogen production technology, Energy policy, Socio-economic on energy, Energy efficiency, planning and management, Life cycle assessment. The journal also welcomes papers on other related topics provided that such topics are within the context of the broader multi-disciplinary scope of developments of renewable energy.
Arjuna Subject : Energi (semua kategori) - Energi Terbarukan, Keberlanjutan dan Lingkungan
Articles 724 Documents
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Two-stage gradient-pore microporous layers for enhanced energy production and durability in PEM fuel cells Alrwashdeh, Saad S.
International Journal of Renewable Energy Development Vol 15, No 3 (2026): May 2026
Publisher : Center of Biomass & Renewable Energy (CBIORE)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61435/ijred.2026.62335

Abstract

Coupled mass, heat, and water transport in proton exchange membrane fuel cells (PEMFCs) critically depend on the microporous layer (MPL), but traditional uniform-pore MPLs are restricted by inherent trade-offs between the accessibility of reactants and the removal of liquid-water. This work presents a two-stage gradient-pore MPL structure and demonstrates its efficiency in terms of a fully coupled, non-isothermal Multiphysics modelling framework, the solution presented is theory-based and mitigates the classical trade-off between gas transport and liquid-water management by introducing a staged pore/porosity architecture that improves oxygen accessibility while promoting directional water evacuation. The proposed design uses a step-pore-size and porosity distribution throughout the MPL thickness to apply a directional capillary pressure gradient so that selective evacuation of water can occur to maintain catalyst-layer hydration. The optimized design is 12 to 18% more peak power density, 10 to 15% higher cell voltage (high current densities 1.5 A.cm-1 and higher), and 30% less cathode liquid saturation than a conventional MPL operating under the same conditions. Thermal analysis also shows that there was 25-35% decrease in temperature non-uniformity, which shows better homogeneity in current density and means that the hotspots causing degradation were caused to fail. Operating-regime mapping validates a strong transition between a transport-limited and optimal performance space, exhibiting increased robustness over a broad operating span. Such findings make pore-gradient engineering a physically based and scalable optimization strategy of improving energy production, thermal stability and durability of next-generation PEM fuel cells concurrently.
Immobilized L-arginine on methacrylate polymer as reusable heterogeneous catalyst for crude palm oil transesterification Erwanto, Erwanto; Warsito, Warsito; Sabarudin, Akhmad; Mardiana, Diah; Iftitah, Elvina Dhiaul
International Journal of Renewable Energy Development Vol 15, No 3 (2026): May 2026
Publisher : Center of Biomass & Renewable Energy (CBIORE)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61435/ijred.2026.61761

Abstract

The development of enviromentally friendly and reusable heterogenous catalyst has attracted significant attention for sustainable biodiesel production from low-cost feedstocks such as crude palm oil (CPO). This study aims to synthesize and evaluate an L-arginine immobilized methacrylate-based porous polymer as an efficient and reusable heterogenous base catalyst for CPO transesterification. In this study, a porous polymer synthesized from glycidyl methacrylate (GM) and ethylene glycol dimethacrylate (EGD), denoted as poly(GM-co-EGD), was employed as a support matrix for L-arginine immobilization to develop an efficient heterogeneous base catalyst for the transesterification of CPO. The catalyst was prepared via free radical polymerization followed by covalent immobilization of L-arginine onto the porous polymer framework. FESEM analysis revealed a well-developed interconnected porous morphology, which was further supported by textural characterization showing a high BET surface area of 650 m² g⁻¹ and a total pore volume of 2.07 cm³ g⁻¹. FTIR spectra confirmed the successful chemical bonding between L-arginine and the polymer matrix. Thermogravimetric analysis indicated good thermal stability of the polymeric catalyst up to 120 °C, suitable for transesterification conditions. The basic strength evaluated using Hammett indicators showed moderate-to-strong basicity (9.9 < H_ < 12), while quantitative back titration with benzoic acid revealed that the catalyst with a poly(GM-co-EGD):L-arginine ratio of 1:2 exhibited the highest total basicity of 1.01 mmol g⁻¹. Process optimization using Response Surface Methodology with a Box–Behnken design produced a highly accurate quadratic model (R² = 0.9992). Under optimal conditions, a biodiesel yield of 82.34 ± 1.08% was achieved, consistent with model predictions. The catalyst maintained stable performance over five consecutive cycles, demonstrating its potential as a green and sustainable catalyst for biodiesel production from CPO.
Robust control strategy for optimized IM-4S-VSI-based wind turbine simulator: Assessment for theoretical study Zerzeri, Mouna; Moussa, Intissar; Khedher, Adel
International Journal of Renewable Energy Development Vol 15, No 3 (2026): May 2026
Publisher : Center of Biomass & Renewable Energy (CBIORE)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61435/ijred.2026.61842

Abstract

Wind turbine emulation faces significant challenges in achieving high dynamic performance while maintaining low-cost and sensorless control architectures suitable for laboratory validation. This paper proposes a software-based wind turbine simulator replicating the dynamic behavior of a 3 kW wind turbine under realistic wind conditions, including quasi-stationary, stochastic, and localized gust (Mexican Hat) profiles. The emulator is implemented using a three-phase induction motor driven by a four-switch voltage source inverter (4S-VSI), controlled via rotor field-oriented control and space vector modulation. A sliding-mode observer (SMO) is employed to estimate rotor speed and flux from stator current measurements, eliminating mechanical sensors. Additionally, an adaptive parameter estimator based on the reactive power method is incorporated into the control loop to identify the rotor resistance in real time. Under nominal loaded operation, the proposed scheme achieves speed tracking errors below 1%, torque errors below 6%, and rotor flux errors below 2% across all wind profiles. When a severe +100% rotor resistance variation is introduced, speed deviation reaches 10% and torque error approaches 20% prior to adaptation, while estimated quantities remain stable, demonstrating observer robustness. Once the reactive power–based adaptation is activated, speed error returns to nearly zero, torque error falls below 5%, stator current error remains under 3%, and flux deviation becomes negligible. The maximum observed speed overshoot under gust excitation is 13.27%, with a settling time of 0.31 s. A quantitative comparison with a conventional six-switch VSI shows that the proposed 4S-VSI reduces switching activity by approximately 43% (from 44.89 kHz to 25.72 kHz equivalent switching frequency), leading to lower switching losses and reduced hardware complexity without compromising dynamic performance. These results demonstrate that the proposed architecture achieves robust observer convergence, accurate wind profile emulation, and significant converter loss reduction, providing a cost-effective and computationally efficient platform for real-time validation of wind energy conversion systems.
Upcycling EAF graphite electrode waste into graphene-oxide–doped PEDOT:PSS for inverted perovskite solar cells Denny, Yus Rama; Fadli, Mohamad; Santoso, Muhammad Iman; Ramdani, Sulaeman Deni; Jafar, Rafa; Meilani, Meilani
International Journal of Renewable Energy Development Vol 15, No 3 (2026): May 2026
Publisher : Center of Biomass & Renewable Energy (CBIORE)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61435/ijred.2026.62013

Abstract

Poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) is widely used as a hole-transport layer (HTL) in inverted perovskite solar cells (PSCs), but its acidity and moisture affinity can limit device performance. This study aimed to evaluate a circular-materials route by upcycling electric-arc-furnace (EAF) graphite-electrode waste into graphene oxide (GO) and applying GO-doped PEDOT:PSS as an HTL modifier, while identifying a practical low-temperature processing window for inverted PSCs under ambient conditions. Graphene oxide was synthesized from EAF graphite waste and dispersed in water (1 mg mL⁻¹), then blended with PEDOT:PSS at different loadings. Inverted PSCs with an ITO/GO-doped PEDOT:PSS/CH₃NH₃PbI₃₋ₓClₓ/PCBM/Ag architecture were fabricated in ambient laboratory air (25–27 °C; RH ≈ 40%) without a glovebox. The effects of GO loading and perovskite annealing temperature (70–130 °C) were evaluated using J–V measurements under AM1.5G illumination, supported by SEM and XRD analyses. Moderate GO addition was associated with improved film coverage and fewer pinholes, while XRD indicated better phase formation near 100 °C. In contrast, excessive annealing (≈130 °C) increased PbI₂ signatures and coincided with severe performance degradation. The optimum condition (600 µL GO per 1 mL PEDOT:PSS and 100 °C annealing) produced a champion power conversion efficiency of 0.80%, with VOC = 0.795 V, JSC = 3.48 mA cm⁻², and FF = 28.9%. Although the efficiency remained modest, the results demonstrated the feasibility of waste-derived GO as a functional PEDOT:PSS interfacial modifier and established a low-temperature processing window governing film integrity and degradation signatures in inverted PSCs, providing a basis for further optimization.

Page 73 of 73 | Total Record : 724

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