Boosting the Efficiency of Dye-Sensitized Solar Cells by a Multifunctional Composite Photoanode to 14.13 .

Angew Chem Int Ed Engl

Institute of Upconversion Nanoscale Materials, College of Chemistry and Molecular Sciences, Henan University, Kaifeng, 475004, China.

Published: June 2023

AI Article Synopsis

  • A new multifunctional composite photoanode is created using TiO hollow spheres, Au nanoparticles, and upconversion nanoparticles, which enhances efficiency in dye-sensitized solar cells.
  • This innovative design achieves a record power conversion efficiency of 14.13%, showcasing its potential for commercial applications in solar technology.
  • The efficiency improvement is attributed to the synergistic effects of light scattering from TiO hollow spheres, near-infrared to visible light conversion by UCNPs, and the surface plasmon resonance of Au nanoparticles, with high stability evidenced by maintaining 95.33% efficiency after 180 hours.

Article Abstract

We report a new strategy to fabricate a multifunctional composite photoanode containing TiO hollow spheres (TiO -HSs), Au nanoparticles (AuNPs) and novel NaYF  : Yb,Er@NaLuF  : Eu@SiO upconversion nanoparticles (UCNPs). The AuNPs are grown on the photoanode film including TiO -HSs and UCNPs by a simple in situ plasmonic treatment. As a result, an impressive power conversion efficiency of 14.13 % is obtained, which is a record for N719 dye-based dye-sensitized solar cells, demonstrating great potential for the solar cells toward commercialization. This obvious enhancement is ascribed to a collaborative mechanism of the TiO -HSs exhibiting excellent light-scattering ability, of the UCNPs converting near-infrared photons into visible photons and of the AuNPs presenting outstanding surface plasmon resonance effect. Notably, a steady-state experiment further reveals that the champion cell exhibits 95.33 % retainment in efficiency even after 180 h of measurements, showing good device stability.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.202302753DOI Listing

Publication Analysis

Top Keywords

solar cells
12
tio -hss
12
dye-sensitized solar
8
multifunctional composite
8
composite photoanode
8
boosting efficiency
4
efficiency dye-sensitized
4
cells multifunctional
4
photoanode 1413 
4
1413  report
4

Similar Publications

High-performance and cost-effective hole-collecting materials (HCMs) are indispensable for commercially viable perovskite solar cells (PSCs). Here, we report an anchorable HCM composed of a triazatruxene core connected with three alkyl carboxylic acid groups (). In contrast to the phosphonic acid-containing tripodal analog (), molecules can form a hydrophilic monolayer on a transparent conducting oxide surface, which is beneficial for subsequent perovskite film deposition in the traditional layer-by-layer fabrication process.

View Article and Find Full Text PDF

Tuning Isomerism Effect in Organic Bulk Additives Enables Efficient and Stable Perovskite Solar Cells.

Nanomicro Lett

January 2025

The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, 324000, People's Republic of China.

Organic additives with multiple functional groups have shown great promise in improving the performance and stability of perovskite solar cells. The functional groups can passivate undercoordinated ions to reduce nonradiative recombination losses. However, how these groups synergistically affect the enhancement beyond passivation is still unclear.

View Article and Find Full Text PDF

Semitransparent perovskite solar cells (ST-PSCs) for building-integrated photovoltaics (BIPV) face the challenge of achieving high efficiency due to significant light loss. The SnO2 electron transport layer (ETL), utilized in n-i-p PSCs and prepared via the sol-gel method, is susceptible to aggregation on substrate, resulting in light scattering that diminishes absorption of the perovskite layer. In this study, we propose a strategy that combines atomic layer deposition (ALD) and sol-gel solution to deposit a bilayer SnO2 structure to address these issues.

View Article and Find Full Text PDF

Heterostructures comprise two or more different semiconducting materials stacked either as co-assemblies or self-sorted based on their dynamics of aggregates. However, self-sorting in heterostructures is rather significant in improving the short exciton diffusion length and charge separation. Despite small organic molecules being known for their self-sorting nature, macrocyclic are hitherto unknown owing to unrestrained assemblies from extended π-conjugated systems.

View Article and Find Full Text PDF

PO Tetrahedron Assisted Chelate Engineering for 10.67%-Efficient Antimony Selenosulfide Solar Cells.

Adv Mater

January 2025

Institute of Thin Film Physics and Applications, Shenzhen Key Laboratory of Advanced Thin Films and Applications, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, State Key Laboratory of Radio Frequency Heterogeneous Integration, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, 518060, China.

Anisotropic carrier transport and deep-level defect of antimony selenosulfide (Sb(S,Se)) absorber are two vital auses restraining the photovoltaic performance of this emerging thin-film solar cell. Herein, chelate engineering is proposed to prepare high-quality Sb(S,Se) film based on hydrothermal deposition approach, which realizes desirable carrier transport and passivated defects by using tetrahedral PO ion in dibasic sodium phosphate (NaHPO, DSP). The PO Lewis structure, on one hand in the form of [(SbO)(PO)] chelate, can adsorb on the polar planes of cadmium sulfide (CdS) layer, promoting the heterogeneous nucleation, and on the other hand, the tetrahedral PO inhibits horizontal growth of (SbS(e)) ribbons due to size effects, thus achieving desirable [hk1] orientation.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!