Increase In Charge Carrier Lifetime Research Articles

Progress in TOPCon solar cell technology: Investigating hafnium oxide through simulation

In the realm of solar energy technology, exploring hafnium oxide (HfO2) in Tunnel Oxide Passivated Contact (TOPCon) solar cells is pivotal. This study delineates HfO2's evolution from semiconductor applications, highlighting its crucial role in enhancing TOPCon solar cell performance. Utilizing ATLAS Silvaco software, the study anticipates a 21.3% increase in charge carrier lifetime through optimized HfO2 layers, addressing challenges in interface engineering and scalability. Innovative research integrates hafnium oxide (HfO2) into TOPCon solar cells, marking a leap in photovoltaic technology. Utilizing ATLAS Silvaco simulations, it shows that HfO2 layers can significantly enhance cell performance, increasing charge carrier lifetime by 21.3% and potentially boosting efficiency by 25%. This underscores HfO2's advantages, like a higher dielectric constant and thermal stability, in improving solar cell efficiency and durability. Future efforts target refining deposition processes, projecting a 25% boost in overall power conversion efficiency (PCE). Emphasizing HfO2's significance in solar cell technology, this research contributes to global sustainable energy initiatives. Integrating HfO2 in TOPCon solar cells signifies a key achievement in harnessing clean, renewable energy. Upcoming research focuses on experimental validation, interface engineering, optimization, stability assessments, scalability, and collaborative studies, aiming to leverage HfO2's potential for elevating solar energy conversion technologies.

In Situ Formation of 2D Perovskite Seeding for Record-Efficiency Indoor Perovskite Photovoltaic Devices.

With 40% efficiency under room light intensity, perovskite solar cells (PSCs) will be promising power supplies for low-light applications, particularly for Internet of Things (IoT) devices and indoor electronics, shall they become commercialized. Herein, β-alaninamide hydrochloride (AHC) is utilized to spontaneously form a layer of 2D perovskite nucleation seeds for improved film uniformity, crystallization quality, and solar cell performance. It is found that the AHC addition indeed improves film quality as demonstrated by better uniformity, lower trap density, smaller lattice stress, and, as a result, a 10-fold increase in charge carrier lifetime. Consequently, not only does the small-area (0.09 cm2 ) PSCs achieve a power conversion efficiency of 42.12%, the large-area cells (1.00 cm2 , and 2.56 cm2 ) attain efficiency as high as 40.93%, and 40.07% respectively. All of these are the highest efficiency values for indoor photovoltaic cells with similar sizes, and more importantly, they represent the smallest efficiency loss due to area scale-up. This work provides a new method to fabricate high-performance indoor PSCs (i-PSCs) for IoT devices with great potential in large-area printing technology.

MOF-Derived Defective Co3O4 Nanosheets in Carbon Nitride Nanocomposites for CO2 Photoreduction and H2 Production

In photocatalysis, especially in CO2 reduction and H2 production, the development of multicomponent nanomaterials provides great opportunities to tune many critical parameters toward increased activity. This work reports the development of tunable organic/inorganic heterojunctions comprised of cobalt oxides (Co3O4) of varying morphology and modified carbon nitride (CN), targeting on optimizing their response under UV-visible irradiation. MOF structures were used as precursors for the synthesis of Co3O4. A facile solvothermal approach allowed the development of ultrathin two-dimensional (2D) Co3O4 nanosheets (Co3O4-NS). The optimized CN and Co3O4 structures were coupled forming heterojunctions, and the content of each part was optimized. Activity was significantly improved in the nanocomposites bearing Co3O4-NS compared with the corresponding bulk Co3O4/CN composites. Transient absorption spectroscopy revealed a 100-fold increase in charge carrier lifetime on Co3O4-NS sites in the composite compared with the bare Co3O4-NS. The improved photocatalytic activity in H2 production and CO2 reduction is linked with (a) the larger interface imposed from the matching 2D structure of Co3O4-NS and the planar surface of CN, (b) improvements in charge carrier lifetime, and (c) the enhanced CO2 adsorption. The study highlights the importance of MOF structures used as precursors in forming advanced materials and the stepwise functionalization of the individual parts in nanocomposites for the development of materials with superior activity.

Functionalization of Pristine, Metallic, and Semiconducting-SWCNTs by ZnO for Efficient Charge Carrier Transfer: Analysis through Critical Coagulation Concentration.

Noncovalent functionalization of single-walled carbon nanotubes (SWCNT) by semiconducting oxides is a majorly sought technique to retain individual properties while creating a synergetic effect for an efficient heterostructure charge transfer. Three types of electronically and optically different SWCNTs: metallic (m), semiconducting (s), and pristine (p) are functionalized by ZnO using a facile sonication method. The physicochemical and morphological properties of the ZnO-functionalized SWCNTs, m-SWCNT+ZnO, s-SWCNT+ZnO, and p-SWCNT+ZnO, are analyzed by advanced characterization techniques. Evidence of charge transfer between SWCNT and ZnO is observed with an increase in charge carrier lifetime from 3.31 ns (ZnO) to 4.76 ns (s-SWCNT+ZnO). To investigate the optimum interaction between SWCNTs and ZnO, critical coagulation concentrations (CCC) are determined using UV–vis absorption spectroscopy for m-SWCNT, s-SWCNT, and p-SWCNT using different molar concentrations of ZnO as the coagulant. The interaction and coagulation mechanisms are described by the modified DLVO theory. Due to the variation in dielectric values and electronic properties of SWCNTs, the CCC values obtained have differed: m-SWCNT (1.9 × 10–4), s-SWCNT (3.4 × 10–4), and p-SWCNT (2 × 10–4). An additional analysis of the aggregates and supernatants of the CCC experiments is also shown to give an insight into the interaction and coagulation processes, explaining the absence of influence exerted by sedimentation and centrifugation.

Кластеры атомов примеси никеля и их влияние на рекомбинационные свойства кремния

The investigation determined the types and nature of structural defects in n-type silicon featuring nickel-dopant atom clusters by using deep-level transient spectroscopy (DLTS) and measuring specific resistance, concentration and lifetime of charge carriers. The investigation employed the Solver-NEXT infrared and atomic-force microscopes. We observed that after high-temperature diffusion star-like defects appear in those Si samples that were cooled slowly. Rapid cooling of Si samples yields no decorating of dislocations, which is linked to formation of [Ni-O]-type point defects, [Ni-Si] silicides and Ni[Nis-Nii] atom pairs (unlike in the case of slowly cooled doped Si samples). The differences in shape and size of the defects forming in slowly and rapidly cooled Si samples may be explained as follows: in the case of slow cooling, as the system transitions into the equilibrium state, its free energy decreases, and nickel atoms gradually precipitating at the defects of the crystal lattice form inclusions characterised by the most energetically favourable state, that is, star-like defects. We detected an increase in charge carrier lifetime caused by formation of a trapping level connected to the [Ni-O] complex in silicon

Where Do Photogenerated Holes Go in Anatase:Rutile TiO2? A Transient Absorption Spectroscopy Study of Charge Transfer and Lifetime

Anatase:rutile TiO2 junctions are often shown to be more photocatalytically active than anatase or rutile alone, but the underlying cause of this improvement is not fully understood. Herein, we employ transient absorption spectroscopy to study hole transfer across the anatase:rutile heterojunction in films as a function of phase composition. By exploiting the different signatures in the photoinduced absorption of trapped charges in anatase and rutile, we were able to separately track the yield and lifetime of holes in anatase and rutile sites within phase composites. Photogenerated holes transfer from rutile to anatase on submicrosecond time scales. This hole transfer can significantly increase the anatase hole yield, with a 20:80 anatase:rutile composite showing a 5-fold increase in anatase holes observed from the microsecond. Hole transfer does not result in an increase in charge-carrier lifetime, where an intermediate recombination dynamic between that of pure anatase (t1/2 ≈ 0.5 ms) and rutile (t1/2 ≈ 20 ms) is found in the anatase:rutile junction (t1/2 ≈ 4 ms). Irrespective of what the formal band energy alignment may be, we demonstrate the importance of trap-state energetics for determining the direction of photogenerated charge separation across heterojunctions and how transient absorption spectroscopy, a method that can specifically track the migration of trapped charges, is a useful tool for understanding this behavior.

Acoustic Enhancement of Polymer/ZnO Nanorod Photovoltaic Device Performance

Acoustic vibrations are shown to enhance the photovoltaic efficiency of a P3HT/ZnO nanorod solar cell by up to 45%, correlated to a three-fold increase in charge carrier lifetime. This is assigned to the generation of piezoelectric dipoles in the ZnO nanorods, indicating that the efficiency of solar cells may be enhanced in the presence of ambient vibrations by the use of piezoelectric materials.

Long-lived charge separated states in nanostructured semiconductor photoelectrodes for the production of solar fuels

The efficient use of sunlight to drive the production of solar fuels requires the photogeneration of suitably long-lived charge separated states capable of driving the multi-electron chemistry of fuel synthesis. Here we discuss a range of promising material design approaches to increasing charge carrier lifetimes, focusing upon semiconductor photoelectrodes for water photolysis and carbon dioxide reduction. Parallels are drawn between the strategies deployed in the development of such artificial systems and those found in natural photosynthesis. We address the use of a range of junctions, including electrolyte/semiconductor, semiconductor/semiconductor and dye sensitized interfaces to provide the spatial separation of charges. A key consideration of the review is the design of such interfaces to achieve a sufficient increase in charge carrier lifetime with a high quantum yield, whilst minimising the energy loss associated with this lifetime gain.

Dramatic increase in charge carrier lifetime in a liquid crystalline perylene bisimide derivative upon bay substitution with chlorine

Download options Please wait... Article information DOI https://doi.org/10.1039/B416407E Article type Paper Submitted 25 Oct 2004 Accepted 05 Jan 2005 First published 25 Jan 2005 Download Citation J. Mater. Chem., 2005,15, 1270-1276 BibTex EndNote MEDLINE ProCite ReferenceManager RefWorks RIS Permissions Request permissions Dramatic increase in charge carrier lifetime in a liquid crystalline perylene bisimide derivative upon bay substitution with chlorine M. G. Debije, Z. Chen, J. Piris, R. B. Neder, M. M. Watson, K. Müllen and F. Würthner, J. Mater. Chem., 2005, 15, 1270 DOI: 10.1039/B416407E To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page. If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given. If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page. Read more about how to correctly acknowledge RSC content. Search articles by author Michael G. Debije Zhijian Chen Jorge Piris Reinhard B. Neder Mark M. Watson Klaus Müllen Frank Würthner