Kamran Hasrat
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Kamran Hasrat has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Fahim Ullah
School of Energy and Power Engineering, Jiangsu University, Zhenjiang 212013, China
2 shared publications - Shuang Wang
School of Energy and Power Engineering, Jiangsu University, Zhenjiang 212013, China
2 shared publications - Mao Mu
School of Energy and Power Engineering, Jiangsu University, Zhenjiang 212013, China
1 shared publication - Sami Iqbal
Southeast University
1 shared publication - Sunel Kumar
School of Energy and Power Engineering, Jiangsu University, Zhenjiang 212013, China
1 shared publication
Latest Publications
- Open Access
Optimizing Solar–Biomass Pyrolysis: Innovations in Reactor Design and Thermal–Solar System Efficiency
To promote renewable energy sources, we focus on optimizing the design of solar–biomass pyrolysis systems. This study suggests the best reactor orientation that creates effective thermal–solar systems for pyrolysis. Solar–biomass pyrolysis uses solar energy to create valuable products like syngas, tar, and char from biomass. This process promotes energy sustainability. We analyze different solar reactors based on their design, operation, heat transfer rate, efficiency, residence time for biomass retention inside the reactor, and biomass conversion efficiency. A thorough analysis of the existing technologies helps to pinpoint the difficulties and most recent developments in the sector, making decision making more manageable and providing information on the viability and sustainability of biomass conversion technologies.
Open AccessOptimizing Solar–Biomass Pyrolysis: Innovations in Reactor Design and Thermal–Solar System Efficiency
To promote renewable energy sources, we focus on optimizing the design of solar–biomass pyrolysis systems. This study suggests the best reactor orientation that creates effective thermal–solar systems for pyrolysis. Solar–biomass pyrolysis uses solar energy to create valuable products like syngas, tar, and char from biomass. This process promotes energy sustainability. We analyze different solar reactors based on their design, operation, heat transfer rate, efficiency, residence time for biomass retention inside the reactor, and biomass conversion efficiency. A thorough analysis of the existing technologies helps to pinpoint the difficulties and most recent developments in the sector, making decision making more manageable and providing information on the viability and sustainability of biomass conversion technologies.
- Open Access
Design and Development of D-A-D Organic Material for Solution-Processed Organic/Si Hybrid Solar Cells with 17.5% Power Conversion Efficiency
Organic/silicon hybrid solar cells have attracted much interest due to their cheap fabrication process and simple device structure. A category of organic substances, Dibenzothiophene–Spirobifluorene–Dithiophene (DBBT-mTPA-DBT), comprises dibenzo [d,b] thiophene and 3-(3-methoxyphenyl)-6-(4-methoxyphenyl)-9H-Carbazole, which function as electron donors. In contrast, methanone is an electron acceptor, with an ∆Est of 3.19 eV. This work focused on hybrid solar cells based on the guest–host phenomena of DBBT-mTPA-DBT and CBP. Using a Si/poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT: PSS) hybrid solar cell with an ultra-thin Dibenzothiophene–Spirobifluorene–Dithienothiophene (DBBT-mTPA-DBT) interlayer between Si and Al led to a PCE of 17.5 ± 2.5%. The DBBT-mTPA-DBT interlayer substantially improved the Si/Al interface, reducing contact resistance from 6.5 × 10⁻1 Ω·cm2 to 3.5 × 10⁻2 Ω·cm2. This improvement increases electron transport efficiency from silicon to aluminum and reduces carrier recombination. The solar cell containing the DBBT-mTPA-DBT/Al double-layer cathode shows a 10.85% increase in power conversion efficiency relative to the standard Al cathode device.
Open AccessDesign and Development of D-A-D Organic Material for Solution-Processed Organic/Si Hybrid Solar Cells with 17.5% Power Conversion Efficiency
Organic/silicon hybrid solar cells have attracted much interest due to their cheap fabrication process and simple device structure. A category of organic substances, Dibenzothiophene–Spirobifluorene–Dithiophene (DBBT-mTPA-DBT), comprises dibenzo [d,b] thiophene and 3-(3-methoxyphenyl)-6-(4-methoxyphenyl)-9H-Carbazole, which function as electron donors. In contrast, methanone is an electron acceptor, with an ∆Est of 3.19 eV. This work focused on hybrid solar cells based on the guest–host phenomena of DBBT-mTPA-DBT and CBP. Using a Si/poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT: PSS) hybrid solar cell with an ultra-thin Dibenzothiophene–Spirobifluorene–Dithienothiophene (DBBT-mTPA-DBT) interlayer between Si and Al led to a PCE of 17.5 ± 2.5%. The DBBT-mTPA-DBT interlayer substantially improved the Si/Al interface, reducing contact resistance from 6.5 × 10⁻1 Ω·cm2 to 3.5 × 10⁻2 Ω·cm2. This improvement increases electron transport efficiency from silicon to aluminum and reduces carrier recombination. The solar cell containing the DBBT-mTPA-DBT/Al double-layer cathode shows a 10.85% increase in power conversion efficiency relative to the standard Al cathode device.