Revealing the Role of Hydrogen in Highly Efficient Ag-Substituted CZTSSe Photovoltaic Devices: Photoelectric Properties Modulation and Defect Passivation.

Nanomicro Lett

The Key Laboratory for Special Functional Materials of MOE, School of Nanoscience and Materials Engineering, National and Local Joint Engineering Research Center for High-Efficiency Display and Lighting Technology, Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng, 475004, People's Republic of China.

Published: December 2024

AI Article Synopsis

  • * While adding silver (Ag) helps reduce these defects, it also causes lower electrical conductivity and carrier density, limiting cell performance.
  • * The proposed solution involves a combined Ag and hydrogen (H) doping method, which enhances conductivity and reduces defects, achieving a notable efficiency of 14.74% in CZTSSe devices.

Article Abstract

The presence of Sn-related defects in CuZnSn(S,Se) (CZTSSe) absorber results in large irreversible energy loss and extra irreversible electron-hole non-radiative recombination, thus hindering the efficiency enhancement of CZTSSe devices. Although the incorporation of Ag in CZTSSe can effectively suppress the Sn-related defects and significantly improve the resulting cell performance, an excellent efficiency has not been achieved to date primarily owing to the poor electrical-conductivity and the low carrier density of the CZTSSe film induced by Ag substitution. Herein, this study exquisitely devises an Ag/H co-doping strategy in CZTSSe absorber via Ag substitution programs followed by hydrogen-plasma treatment procedure to suppress Sn defects for achieving efficient CZTSSe devices. In-depth investigation results demonstrate that the incorporation of H in Ag-based CZTSSe absorber is expected to improve the poor electrical-conductivity and the low carrier density caused by Ag substitution. Importantly, the C=O and O-H functional groups induced by hydrogen incorporation, serving as an electron donor, can interact with under-coordinated cations in CZTSSe material, effectively passivating the Sn-related defects. Consequently, the incorporation of an appropriate amount of Ag/H in CZTSSe mitigates carrier non-radiative recombination, prolongs minority carrier lifetime, and thus yields a champion efficiency of 14.74%, showing its promising application in kesterite-based CZTSSe devices.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11615170PMC
http://dx.doi.org/10.1007/s40820-024-01574-3DOI Listing

Publication Analysis

Top Keywords

sn-related defects
12
cztsse absorber
12
cztsse devices
12
cztsse
11
non-radiative recombination
8
poor electrical-conductivity
8
electrical-conductivity low
8
low carrier
8
carrier density
8
revealing role
4

Similar Publications

Energy Band Alignment and Defect Synergistic Regulation Enable Air-Solution-Processed Kesterite Solar Cells With the Lowest V Deficit.

Adv Mater

November 2024

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.

The major challenge in preparing high-performance CuZnSn(S,Se) solar cells is the large open circuit voltage deficit (V-def). A new strategy utilizing the synergistic substitution of Ag and In dual cations has been proposed to simultaneously address the problems of undesirable interface band alignment and high-density detrimental bulk defects, obtaining decreased carrier recombination rate and increased minority carrier lifetime. The shorter In-S/Se bonds move the CBM higher by generating stronger repulsive force than the Sn-S/Se bonds, thus adjusting the interface band alignment.

View Article and Find Full Text PDF
Article Synopsis
  • - All-perovskite tandem solar cells could exceed the efficiency limits of traditional solar cells, but their performance is currently restricted by defects that cause energy losses in the material.
  • - Researchers developed a method using a surface polishing agent and a passivator to fix defects in Sn-Pb mixed perovskite films, improving the film quality and reducing non-radiative energy loss.
  • - The optimized solar cells achieved power conversion efficiencies of 22.65% and 23.32%, with a certified efficiency of 28.49% for two-junction all-perovskite tandem cells, indicating significant progress in solar technology.
View Article and Find Full Text PDF

Segmented Control of Selenization Environment for High-Quality CuZnSn(S,Se) Films Toward Efficient Kesterite Solar Cells.

Small Methods

December 2024

Key Laboratory for Special Functional Materials of MOE, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, Collaborative Innovation Center of Nano Functional Materials and Applications, School of Materials, Henan University, Kaifeng, 475004, China.

Article Synopsis
  • High-quality CZTSSe solar cells require improved crystal structure and fewer defects for better open-circuit voltage and efficiency.
  • A new segmented control strategy for the selenization process is introduced to better manage the evaporation of selenium, which enhances film quality during growth.
  • This method reduces defects and improves carrier collection, achieving a solar cell efficiency of 13.77% with low voltage deficit.
View Article and Find Full Text PDF

Tin halide perovskite solar cells (PSCs) are regarded as the most promising lead-free alternatives for photovoltaic applications. However, they still suffer from uncompetitive photovoltaic performance because of the facile Sn oxidation and Sn-related defects. Herein, a defect and carrier management strategy by using diaminopyridine (DP) and 4-bromo-2,6-diaminopyridine (4BrDP) as multifunctional additives for tin halide perovskites is reported.

View Article and Find Full Text PDF

Severe nonradiative recombination and open-circuit voltage loss triggered by high-density interface defects greatly restrict the continuous improvement of Sn-based perovskite solar cells (Sn-PVSCs). Herein, a novel amphoteric semiconductor, O-pivaloylhydroxylammonium trifluoromethanesulfonate (PHAAT), is developed to manage interface defects and carrier dynamics of Sn-PVSCs. The amphiphilic ionic modulators containing multiple Lewis-base functional groups can synergistically passivate anionic and cationic defects while coordinating with uncoordinated Sn to compensate for surface charge and alleviate the Sn oxidation.

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!