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Xueyun Wang

Bio: Xueyun Wang is an academic researcher from Beijing Institute of Technology. The author has contributed to research in topics: Ferroelectricity & Materials science. The author has an hindex of 20, co-authored 94 publications receiving 1842 citations. Previous affiliations of Xueyun Wang include Rutgers University & University of Science and Technology Beijing.


Papers
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Journal ArticleDOI
TL;DR: Li et al. as discussed by the authors employed fluoride to simultaneously passivate both anion and cation vacancies, by taking advantage of the extremely high electronegativity of fluoride, and obtained a power conversion efficiency of 21.46% (and a certified 21.3%-efficient cell) in a device based on the caesium, methylammonium (MA), and formamidinium (FA) triple-cation perovskite (Cs0.05FA0.41)Pb(I0.98Br0.02)3 treated with sodium
Abstract: Defects play an important role in the degradation processes of hybrid halide perovskite absorbers, impeding their application for solar cells. Among all defects, halide anion and organic cation vacancies are ubiquitous, promoting ion diffusion and leading to thin-film decomposition at surfaces and grain boundaries. Here, we employ fluoride to simultaneously passivate both anion and cation vacancies, by taking advantage of the extremely high electronegativity of fluoride. We obtain a power conversion efficiency of 21.46% (and a certified 21.3%-efficient cell) in a device based on the caesium, methylammonium (MA) and formamidinium (FA) triple-cation perovskite (Cs0.05FA0.54MA0.41)Pb(I0.98Br0.02)3 treated with sodium fluoride. The device retains 90% of its original power conversion efficiency after 1,000 h of operation at the maximum power point. With the help of first-principles density functional theory calculations, we argue that the fluoride ions suppress the formation of halide anion and organic cation vacancies, through a unique strengthening of the chemical bonds with the surrounding lead and organic cations. Defects and defect migration are detrimental for perovskite solar cell efficiency and long-term stability. Li et al. show that fluoride is able to suppress the formation of halide anion and organic cation vacancy defects by restraining the relative ions via ionic and hydrogen bonds.

723 citations

Journal ArticleDOI
TL;DR: In this paper, a giant electromechanical d33 coefficient 110pC∕N is obtained in ferroelectric V-doped ZnO films, which is nearly one order of magnitude higher than that of undoped samples.
Abstract: A giant electromechanical d33 coefficient 110pC∕N is obtained in ferroelectric V-doped ZnO films, which is nearly one order of magnitude higher than that of undoped samples. It is considered that the switchable spontaneous polarization induced by V dopants and the accompanying relatively high permittivity should be responsible for the enhancement of piezoelectric response. Moreover, from another point of view, an easier rotation of V–O bonds which are noncollinear with c axis under electric field might be the microscopic origin of this anomaly. The improved piezoelectric properties could make V-doped ZnO a promising candidate for piezoelectric devices.

189 citations

Journal ArticleDOI
30 Jul 2021-Science
TL;DR: In this paper, a liquid medium annealing (LMA) technology is used to create a robust chemical environment and constant heating field to modulate crystal growth over the entire film, which produces films with high crystallinity, fewer defects, desired stoichiometry, and overall film homogeneity.
Abstract: Solution processing of semiconductors is highly promising for the high-throughput production of cost-effective electronics and optoelectronics. Although hybrid perovskites have potential in various device applications, challenges remain in the development of high-quality materials with simultaneously improved processing reproducibility and scalability. Here, we report a liquid medium annealing (LMA) technology that creates a robust chemical environment and constant heating field to modulate crystal growth over the entire film. Our method produces films with high crystallinity, fewer defects, desired stoichiometry, and overall film homogeneity. The resulting perovskite solar cells (PSCs) yield a stabilized power output of 24.04% (certified 23.7%, 0.08 cm2) and maintain 95% of their initial power conversion efficiency (PCE) after 2000 hours of operation. In addition, the 1-cm2 PSCs exhibit a stabilized power output of 23.15% (certified PCE 22.3%) and keep 90% of their initial PCE after 1120 hours of operation, which illustrates their feasibility for scalable fabrication. LMA is less climate dependent and produces devices in-house with negligible performance variance year round. This method thus opens a new and effective avenue to improving the quality of perovskite films and photovoltaic devices in a scalable and reproducible manner.

164 citations

Journal ArticleDOI
TL;DR: In this paper, an imaging study of vortex proliferation near a continuous phase transition in a ferroelectric reveals frozen-in vortices that follow the predictions of the Kibble-Zurek model for cosmological strings formed in the early Universe.
Abstract: An imaging study of vortex proliferation near a continuous phase transition in a ferroelectric reveals frozen-in vortices that follow the predictions of the Kibble–Zurek model for cosmological strings formed in the early Universe.

158 citations

Journal ArticleDOI
TL;DR: In this article, an in situ cross-linking polymerizable propargylammonium (PA+) was introduced to the 3D perovskite film at surfaces and grain boundaries to form a 1D/3D polygonal heterostructure.
Abstract: Long-term stability is an essential requirement for perovskite solar cells (PSCs) to be commercially viable. Heterojunctions built by low-dimensional and three-dimensional perovskites (1D/3D or 2D/3D) help to improve the stability of PSCs. However, the insulated organic cations of low-dimensional perovskite impede the transport of carriers, decreasing the power conversion efficiency (PCE) of PSCs. Herein, we introduce an in situ cross-linking polymerizable propargylammonium (PA+) to the 3D perovskite film at surfaces and grain boundaries to form a 1D/3D perovskite heterostructure. This passivation strategy not only significantly improves the interfacial carrier transport but also releases residual tensile strain in perovskite films. As a result, the corresponding devices achieve a champion PCE of 21.19%, while maintaining 93% of their initial efficiency after 3055 h of continuous illumination under maximum power point (MPP) operating conditions.

110 citations


Cited by
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TL;DR: In this article, a review of multiferroic thin-film heterostructures, device architectures, and domain and interface effects is presented. But the focus of the field is now shifting into neighbouring research areas, as discussed in this review.
Abstract: Materials with a coexistence of magnetic and ferroelectric order — multiferroics — provide an efficient route for the control of magnetism by electric fields. The study of multiferroics dates back to the 1950s, but in recent years, key discoveries in theory, synthesis and characterization techniques have led to a new surge of interest in these materials. Different mechanisms, such as lone-pair, geometric, charge-ordering and spin-driven effects, can support multiferroicity. The general focus of the field is now shifting into neighbouring research areas, as we discuss in this Review. Multiferroic thin-film heterostructures, device architectures, and domain and interface effects are explored. The violation of spatial and inversion symmetry in multiferroic materials is a key feature because it determines their properties. Other aspects, such as the non-equilibrium dynamics of multiferroics, are underrated and should be included in the topics that will define the future of the field. Multiferroic materials exhibit magnetic and ferroelectric order at the same time and provide a way to control magnetism with electric fields. We discuss the mechanisms supporting multiferroicity, multiferroic thin films and heterostructures, the non-equilibrium dynamics of multiferroics, fundamental symmetry issues and the impact of multiferroics on other research areas.

922 citations

Journal ArticleDOI
TL;DR: In this article, the authors acknowledge the use of KAUST Core Lab and KAust Solar Center facilities for the purpose of solar energy research under award no. OSR-2017-CRG-3380.
Abstract: We acknowledge the use of KAUST Core Lab and KAUST Solar Center facilities. This work was supported by KAUST and the Office of Sponsored Research (OSR) under award no. OSR-2017-CRG-3380. F.G. is a Wallenberg Academy Fellow.

783 citations

Journal ArticleDOI
20 Dec 2019-Science
TL;DR: The chemical environment of a functional group that is activated for defect passivation was systematically investigated with theophylline, caffeine, and theobromine and hydrogen-bond formation between N-H and I (iodine) assisted the primary C=O binding with the antisite Pb defect to maximize surface-defect binding.
Abstract: Surface trap–mediated nonradiative charge recombination is a major limit to achieving high-efficiency metal-halide perovskite photovoltaics. The ionic character of perovskite lattice has enabled molecular defect passivation approaches through interaction between functional groups and defects. However, a lack of in-depth understanding of how the molecular configuration influences the passivation effectiveness is a challenge to rational molecule design. Here, the chemical environment of a functional group that is activated for defect passivation was systematically investigated with theophylline, caffeine, and theobromine. When N-H and C=O were in an optimal configuration in the molecule, hydrogen-bond formation between N-H and I (iodine) assisted the primary C=O binding with the antisite Pb (lead) defect to maximize surface-defect binding. A stabilized power conversion efficiency of 22.6% of photovoltaic device was demonstrated with theophylline treatment.

684 citations

Journal ArticleDOI
TL;DR: In this paper, the predominant pathways that contribute to non-radiative recombination losses in perovskite solar cells, and evaluate their impact on device performance are analyzed, and some notable advances in mitigating these losses are highlighted.
Abstract: Photovoltaic solar cells based on metal halide perovskites have gained considerable attention over the past decade because of their potentially low production cost, earth-abundant raw materials, ease of fabrication and ever-increasing power conversion efficiencies of up to 25.2%. This type of solar cells offers the promise of generating electricity at a more competitive unit price than traditional fossil fuels by 2035. Nevertheless, the best research cell efficiencies are still below the theoretical limit defined by the Shockley-Queissier theory owing to the presence of non-radiative recombination losses. In this Review, we analyse the predominant pathways that contribute to non-radiative recombination losses in perovskite solar cells, and evaluate their impact on device performance. We then discuss how non-radiative recombination losses can be estimated through reliable characterization techniques, and highlight some notable advances in mitigating these losses, which hint at pathways towards defect-free perovskite solar cells. Finally, we outline directions for future work that will push the efficiency of perovskite solar cells towards the radiative limit.

644 citations