scispace - formally typeset
Search or ask a question
Author

Jinbiao Jia

Bio: Jinbiao Jia is an academic researcher from Qufu Normal University. The author has contributed to research in topics: Perovskite (structure) & Perovskite solar cell. The author has an hindex of 9, co-authored 18 publications receiving 201 citations.

Papers
More filters
Journal ArticleDOI
TL;DR: In this article, rare-earth doped upconversion nanoparticles with core-shell structure are synthesized for enhancing the performance of perovskite solar cells, which can be used as spectral conversion materials.

61 citations

Journal ArticleDOI
Wentao Qi1, Wen Jiang1, Fan Xu1, Jinbiao Jia1, Chao Yang1, Bingqiang Cao1 
TL;DR: In this article, a hollow nanosphere structure with CeO2 shell/ultrathin nitrogen-doped carbon shell as highly efficient host for lithium-sulfur batteries was designed.

55 citations

Journal ArticleDOI
TL;DR: In this paper, a green mixed anti-solvent of ethylacetate with isopropanol was used to improve the surface morphology and passivate the grainboundary/surface defects of perovskite film.

37 citations

Journal ArticleDOI
TL;DR: In this article, the down-conversion nanocrystals film made of europium-doped sodium yttrium fluoride was deposited on the nonconducting side of the conducting glass.
Abstract: Perovskite solar cells assembled with titanium dioxide electron transport layer exhibited brilliant photovoltaic properties due to titanium dioxide having a high electron mobility, appropriate energy level alignment and easy fabrication procedure. However, inherent instability exists in titanium dioxide-based perovskite solar cells because of the ultraviolet photocatalytic activity of titanium dioxide. This results in recombination at the interface of titanium dioxide/perovskite. In this report, the down-conversion nanocrystals film made of europium-doped sodium yttrium fluoride was deposited on the non-conducting side of the conducting glass. The down-conversion nanocrystal layer could absorb high energy ultraviolet photons and converted them to visible light. The layer not only extended the spectral response range for perovskite solar cells but also alleviated the photocatalytic activity of titanium dioxide. The perovskite solar cells with the down-conversion nanocrystals film generated average power conversion efficiency yield of 19.99%, which is much better than that of the device without the down-conversion nanocrystals film (16.99%). The best power conversion efficiency for the device with the down-conversion nanocrystals film was 20.17%. In addition, perovskite solar cells with the down-conversion nanocrystals film showed a small hysteresis.

36 citations

Journal ArticleDOI
29 Oct 2019
TL;DR: The investigation demonstrates that the rare-earth doping is low-cost and effective method to improve the photovoltaic performance of SnO2-based PSCs.
Abstract: Tin oxide (SnO2), as electron transport material to substitute titanium oxide (TiO2) in perovskite solar cells (PSCs), has aroused wide interests. However, the performance of the PSCs based on SnO2 is still hard to compete with the TiO2-based devices. Herein, a novel strategy is designed to enhance the photovoltaic performance and long-term stability of PSCs by integrating rare-earth ions Ln3+ (Sc3+, Y3+, La3+) with SnO2 nanospheres as mesoporous scaffold. The doping of Ln promotes the formation of dense and large-sized perovskite crystals, which facilitate interfacial contact of electron transport layer/perovskite layer and improve charge transport dynamics. Ln dopant optimizes the energy level of perovskite layer, reduces the charge transport resistance, and mitigates the trap state density. As a result, the optimized mesoporous PSC achieves a champion power conversion efficiency (PCE) of 20.63% without hysteresis, while the undoped PSC obtains an efficiency of 19.01%. The investigation demonstrates that the rare-earth doping is low-cost and effective method to improve the photovoltaic performance of SnO2-based PSCs.

35 citations


Cited by
More filters
Journal ArticleDOI
TL;DR: This review covers the key criteria for rare-earth doping, including basic electronic structures, lattice environments, and doping strategies, as well as fundamental design principles that enhance the electrical, optical, catalytic, and magnetic properties of the material.
Abstract: Impurity doping is a promising method to impart new properties to various materials. Due to their unique optical, magnetic, and electrical properties, rare-earth ions have been extensively explored as active dopants in inorganic crystal lattices since the 18th century. Rare-earth doping can alter the crystallographic phase, morphology, and size, leading to tunable optical responses of doped nanomaterials. Moreover, rare-earth doping can control the ultimate electronic and catalytic performance of doped nanomaterials in a tunable and scalable manner, enabling significant improvements in energy harvesting and conversion. A better understanding of the critical role of rare-earth doping is a prerequisite for the development of an extensive repertoire of functional nanomaterials for practical applications. In this review, we highlight recent advances in rare-earth doping in inorganic nanomaterials and the associated applications in many fields. This review covers the key criteria for rare-earth doping, including basic electronic structures, lattice environments, and doping strategies, as well as fundamental design principles that enhance the electrical, optical, catalytic, and magnetic properties of the material. We also discuss future research directions and challenges in controlling rare-earth doping for new applications.

188 citations

Journal ArticleDOI
TL;DR: In this article, the authors discuss the major advances and the updated state-of-the-art in the carbon-based perovskite solar cells scenario, keeping a solid trajectory where the accessibility, low cost, high electrical conductivity, chemical stability and controllable porosity of carbon are highlighted and exploited in the design of upscalable hybrid solar cells.
Abstract: Almost ten years after their first use in the photovoltaic (PV) field, perovskite solar cells (PSCs) are now hybrid devices that, in addition to having reached silicon performance, can accelerate the energy transition and boost the use of abundant elements for their manufacturing process. However, noble metals (in particular gold) represent the most typically used sources for back electrode fabrication, and this issue has been intensively considered by the research community in the last five years. This review shows how the most promising solution, considering also the need to develop a large-scale production process, is based on the use of carbon-based materials for the preparation of back electrodes. Graphite, carbon black, graphene and carbon nanotubes (CNTs) have been proposed, functionalized and characterized, leading to laboratory-scale solar cells and modules capable of providing excellent efficiencies and ensuring stability greater than those of gold-based devices. Strengthened by these results and its hydrophobizing properties, carbon has also started to be used as an electron transporting material (ETM), with excellent results on both rigid and flexible substrates. This review discusses the major advances and the updated state-of-the-art in the carbon-based PSC scenario, keeping a solid trajectory where the accessibility, low cost, high electrical conductivity, chemical stability and controllable porosity of carbon are highlighted and exploited in the design of upscalable hybrid solar cells.

154 citations

Journal ArticleDOI
TL;DR: In this paper, a review of perovskite-based solar cells is presented, focusing on the recent progress in morphology optimizations by various processing conditions such as annealing condition, additive effects, Lewis acid base adduct approach, precursor solution aging and post-device ligand treatment emphasizing on grain sizes, film uniformity, defect passivation, ambient compatibility and device efficiency and stability.
Abstract: Hybrid organic–inorganic halide perovskite based solar cell technology has passed through a phase of unprecedented growth in the efficiency scale from 3.8% to above 25% within a decade. This technology has drawn tremendous research interest because of facile solution processability, ease of large scale manufacturing and ultra-low cost production of perovskite based thin film solar cells. It has been observed that performances of perovskite-based solar cells are extremely dependent on the morphology and crystallinity of the perovskite layer. The high-quality perovskite films have made a significant impact on the fabrication of efficient and stable hybrid perovskite solar cells. It has also been observed that device lifetime depends on the perovskite morphology; devices with larger perovskite grains degrade slowly than those of the smaller ones. Various methods of perovskite growth such as sequential deposition, doctor blading, slot die coating and spray coating have been applied to achieve the most appropriate morphology necessary for highly efficient and stable solar cells. This review focuses on the recent progress in morphology optimizations by various processing condition such as annealing condition, additive effects, Lewis acid–base adduct approach, precursor solution aging and post-device ligand treatment emphasizing on grain sizes, film uniformity, defect passivation, ambient compatibility and device efficiency and stability. In this review, we also discussed recently developed bifacial stamping technique and deposition methods for large-area and roll-to-roll fabrication of highly efficient and stable perovskite solar cells.

128 citations

Journal ArticleDOI
22 Jul 2019
TL;DR: Lead halide perovskites have displayed the highest solar power conversion efficiencies of 23% but the toxicity issues of these materials need to be addressed to ensure clean and green photovoltaic technology.
Abstract: Lead halide perovskites have displayed the highest solar power conversion efficiencies of 23% but the toxicity issues of these materials need to be addressed. Lead-free perovskites have emerged as viable candidates for potential use as light harvesters to ensure clean and green photovoltaic technology. The substitution of lead by Sn, Ge, Bi, Sb, Cu and other potential candidates have reported efficiencies of up to 9%, but there is still a dire need to enhance their efficiencies and stability within the air. A comprehensive review is given on potential substitutes for lead-free perovskites and their characteristic features like energy bandgaps and optical absorption as well as photovoltaic parameters like open-circuit voltage (V OC), fill factor, short-circuit current density (J SC), and the device architecture for their efficient use. Lead-free perovskites do possess a suitable bandgap but have low efficiency. The use of additives has a significant effect on their efficiency and stability. The incorporation of cations like diethylammonium, phenylethyl ammonium, phenylethyl ammonium iodide, etc., or mixed cations at different compositions at the A-site is reported with engineered bandgaps having significant efficiency and stability. Recent work on the advancement of lead-free perovskites is also reviewed.

112 citations

Journal ArticleDOI
TL;DR: In this article, a detailed structural, compositional and micro-structural characterization of perovskite layers fabricated by 14 different antisolvents is presented, where the authors identify two key factors that influence the quality of the perov-skite active layer: the solubility of the organic precursors in the antisolvent and its miscibility with the host solvent(s) of the pre-treatment solution.
Abstract: Deposition of perovskite thin films by antisolvent engineering is one of the most common methods employed in perovskite photovoltaics research. Herein, we report on a general method that allows the fabrication of highly efficient perovskite solar cells by any antisolvent via the manipulation of the antisolvent application rate. Through a detailed structural, compositional and microstructural characterization of perovskite layers fabricated by 14 different antisolvents, we identify two key factors that influence the quality of the perovskite active layer: the solubility of the organic precursors in the antisolvent and its miscibility with the host solvent(s) of the perovskite precursor solution. Depending on these two factors, each antisolvent can be utilized to produce high performance devices reaching power conversion efficiencies (PCEs) that exceed 21%. Moreover, we demonstrate that by employing the optimal antisolvent application procedure, highly efficient solar cells can be fabricated from a broad range of precursor stoichiometries, with either a significant excess or deficiency of organic iodides.

111 citations