Publications by authors named "Dejian Yu"

Article Synopsis
  • 2D Ruddlesden-Popper perovskites (RPPs) are gaining popularity for their environmental stability, but their power conversion efficiency (PCE) remains lower than traditional 3D perovskite solar cells due to issues with carrier transport and phase heterogeneity.
  • The introduction of binary spacers like n-butylammonium and benzamidine helps improve the crystallization process, leading to more uniform phase distribution and enhanced carrier transport in RPP films.
  • The research achieved a record high PCE of 21.15% and an open circuit voltage of 1.26 V for low n-value RPP solar cells by using these spacers and high-quality single crystal structures, which also reduced
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Deep-level traps at the buried interface of perovskite and energy mismatch problems between the perovskite layer and heterogeneous interfaces restrict the development of ideal homogenized films and efficient perovskite solar cells (PSCs) using the one-step spin-coating method. Here, we strategically employed sparingly soluble germanium iodide as a homogenized bulk in-situ reconstruction inducing material preferentially aggregated at the perovskite buried interface with gradient doping, markedly reducing deep-level traps and withstanding local lattice strain, while minimizing non-radiative recombination losses and enhancing the charge carrier lifetime over 9 µs. Furthermore, this gradient doping assisted in modifying the band diagram at the buried interface into a desirable flattened alignment, substantially mitigating the energy loss of charge carriers within perovskite films and improving the carrier extraction equilibrium.

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Article Synopsis
  • Two-terminal (2T) perovskite-based tandem solar cells (TSCs) aim to exceed the efficiency limits of single-junction solar cells by using subcells with varying bandgaps, but their current highest efficiency of 33.9% is still below the theoretical maximum of 42-43%.
  • A major challenge for enhancing the effectiveness of these TSCs is the design of transparent recombination layers (RLs) that must manage optical losses, contact resistance, and other performance criteria between the subcells.
  • The review discusses the role and requirements of RLs, highlights characterization methods for research, and identifies key factors hindering RL performance improvements along with potential future research directions.
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Despite their excellent environmental stability, low defect density, and high carrier mobility, large-n quasi-two-dimensional halide perovskites (quasi-2DHPs) feature a limited application scope because of the formation of self-assembled multiple quantum wells (QWs) due to the similar thermal stabilities of large-n phases. However, large-n quasi-phase-pure 2DHPs (quasi-PP-2DHPs) can solve this problem perfectly. This review discusses the structures, formation mechanisms, and photoelectronic and physical properties of quasi-PP-2DHPs, summarises the corresponding single crystals, thin films, and heterojunction preparation methods, and presents the related advances.

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ConspectusThree-dimensional (3D) halide perovskite (HP) solar cells have been thriving as promising postsilicon photovoltaic systems. However, despite the decency of efficiency, they suffer from poor stability. Partial dimensionality reduction from 3D to 2D was found to significantly meliorate the instability, thus mixed-dimensional 2D/3D HP solar cells have been expected to combine favorable durability and high efficiency.

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Mixed-dimensional 2D/3D halide perovskite solar cells promise high stability but practically deliver poor power conversion efficiency, and the 2D HP component has been held as the culprit because its intrinsic downsides (ill charge conductivity, wider bandgap, and strong exciton binding) were intuitively deemed to hinder carrier transport. Herein, we show that the 2D HP fragments, in fact, allow free migration of carriers in darkness but only block the carrier transport under illumination. While surely limiting the photovoltaic performance, such photoinduced carrier blocking effect is unexplainable by the traditional understanding above but is found to stem from the trap-filling-enhanced built-in potential of the 2D/3D HP interface.

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The global warming caused by greenhouse gas emissions has received widespread attention from all around the world. In this regard, how to calculate the carbon footprint (CF) scientifically and accurately produced by human activities to achieve emission reduction goals has been widely discussed by scholars. In recent years, related research on this issue has increased, leading to a significant expand in the number of publications.

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Miniaturized multispectral detectors are urgently desired given the unprecedented prosperity of smart optoelectronic chips for integrated functions including communication, imaging, scientific analysis, etc. However, multispectral detectors require complicated prism optics or interference/interferometric filters for spectral recognition, which hampers the miniaturization and their subsequent integration in photonic integrated circuits. In this work, inspired by the advance of computational imaging, optical-component-free miniaturized multispectral detector on 4 mm gradient bandgap MAPbX microwire with a diameter of 30 µm, is reported.

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In this work, we proposed a fluorescence conversion layer with polarization characteristics to enhance UV polarization detection for the first time. To achieve this goal, the colloidal lead halide CsPbBr nanowires (NWs) with appropriate lengths were synthesized by the method of ultrasonication synthesis assisted by the addition of hydrobromic acid (HBr) ligands. By adding HBr, the properties of synthesized NWs are improved, and due to the controllable perovskite-stretched NWs, polymer composite films were fabricated, which can generate photoluminescence (PL) with strong polarization.

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Photodetectors selective to the polarization empower breakthroughs in sensing technology for target identification. However, the realization of polarization-sensitive photodetectors based on intrinsically anisotropic crystal structure or extrinsically anisotropic device pattern requires complicated epitaxy and etching processes, which limit scalable production and application. Here, solution-processed PEA MA (Sn Pb ) I (PEA= phenylethylammonium, MA= methylammonium) polycrystalline film is probed as photoactive layer toward sensing polarized photon from 300 to 1050 nm.

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Due to the rapid development of smart technology infusion, visible light communication (VLC) has been promising as a connection belt among real estates due to the appealing features including fast speed of data transmission and high bandwidth. Unfortunately, the issues of crosstalk, interference, or data leakage in the VLC impose rigorous requests for the receiver terminal, photodetector, including fast and accurate signal recognition, rapid decoding, etc. In pursuit of distinctive merits, a dual-band photodetector is proposed as an efficient receiver terminal for VLC in this work.

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Ensuring nuclear safety has become of great significance as nuclear power is playing an increasingly important role in supplying worldwide electricity. β-ray monitoring is a crucial method, but commercial organic scintillators for β-ray detection suffer from high temperature failure and irradiation damage. Here, we report a type of β-ray scintillator with good thermotolerance and irradiation hardness based on a two-dimensional halide perovskite.

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Fluorescence imaging with photodetectors (PDs) toward near-infrared I (NIR-I) photons (700-900 nm), the so-called "optical window" in organisms, has provided an important path for tracing biological processes in vivo. With both excitation photons and fluorescence photons in this narrow range, a stringent requirement arises that the fluorescence signal should be efficiently differentiated for effective sensing, which cannot be fulfilled by common PDs with a broadband response such as Si-based PDs. In this work, delicate optical microcavities are designed to develop a series of bionic PDs with selective response to NIR-I photons, the merits of a narrowband response with a full width at half maximum (FWHM) of <50 nm, and tunability to cover the NIR-I range are highlighted.

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Halide perovskite (HP) nanocrystals (NCs) have recently shown great potential for X-ray detection and imaging. However, the practical application still has a long way to go with many technical requirements waiting to be fulfilled, including structure optimization, stability enhancement, and cost reduction. A design principle in this beginning stage is urgently needed but still lacking.

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Benefiting from morphology-/size-tunable optical features, nanocrystals have been considered promising candidates for display or lighting applications. To achieve selective characteristic emission, precise control in size and morphology is thus a prerequisite. Herein, we report that the nanosecond-pulsed laser irradiation induces CsPbBr reshaping, yielding precise control of size and morphology.

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Halide perovskites (HPs) with α-phase have been intensively explored as light absorbers in solar cells, while δ-phase HPs are not suitable for photoelectric application owing to their wider bandgap and less competitive semiconducting properties. Here we propose an innovative light-controlled nanorotor based on δ-CsPb(Br/I)3 nanorods. The one-dimensional lattice structure enables habitual growth of single-crystalline nanorods upon controllable iodide incorporation.

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The past several years have witnessed tremendous developments of metal halide perovskite (MHP)-based optoelectronics. Particularly, the intensive research of MHP-based light-emitting diodes, photodetectors, and solar cells could probably reform the optoelectronic semiconductor industry. In comparison, in spite of the large intrinsic charge carrier mobility of MHPs, the development of MHP-based field-effect transistors (MHP-FETs) is relatively slow, which is essentially due to the gate-field screening effect induced by the ion migration and accumulation in MHP-FETs.

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Inorganic halide perovskites exhibited promising potentials for high-performance wide-band photodetectors (PDs) due to their high light absorption coefficients, long carrier diffusion length and wide light absorption ranges. Here, we report two-dimensional (2D) CsPbBr/PCBM heterojunctions for sensitive, fast and flexible PDs, whose performances can be greatly boosted by the charge transfer through the energy-aligned interface. The 2D CsPbBr nanosheets with high crystallinity were fabricated via a simple solution-process at room temperature, and then assembled into flexible heterojunctions films with polymerphenyl-C61-butyric acid methyl ester (PCBM).

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Transition metal dichalcogenides (TMDs) are promising candidates for flexible optoelectronic devices because of their special structures and excellent properties, but the low optical absorption of the ultrathin layers greatly limits the generation of photocarriers and restricts the performance. Here, we integrate all-inorganic perovskite CsPbBr nanosheets with MoS atomic layers and take the advantage of the large absorption coefficient and high quantum efficiency of the perovskites, to achieve excellent performance of the TMD-based photodetectors. Significantly, the interfacial charge transfer from the CsPbBr to the MoS layer has been evidenced by the observed photoluminescence quenching and shortened decay time of the hybrid MoS/CsPbBr.

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The challenge of detecting research topics in a specific research field has attracted attention from researchers in the bibliometrics community. In this study, to solve two problems of clustering papers, i.e.

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Low-dimensional halide perovskite (HP) has triggered lots of research attention in recent years due to anisotropic optoelectronic/semiconducting properties and enhanced stability. High-quality low-dimensional HPs via controllable engineering are required to fulfill the encouraging promise for device applications. Here, we introduce, for the first time, postsynthetic ultrasonic-assisted refinement of two-dimensional homologous HPs (OAPbBr, OA is octadecylamine).

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With regards to developing miniaturized coherent light sources, the temperature-insensitivity in gain spectrum and threshold is highly desirable. Quantum dots (QDs) are predicted to possess a temperature-insensitive threshold by virtue of the separated electronic states; however, it is never observed in colloidal QDs due to the poor thermal stability. Besides, for the classical II-VI QDs, the gain profile generally redshifts with increasing temperature, plaguing the device chromaticity.

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Two-dimensional (2D) homologous halide perovskite (HP) microcrystallines have emerged as a promising alternative light-sensitive material; however, the undesirable quantum confinement effect and severe interfacial charge-carrier scattering still hamper their applications in photodetectors (PDs). Here we propose a novel postsynthetic treatment to simultaneously solve both problems. 2D (OA)FAPbBr (OA and FA represent octadecylamine and formamidine) microplatelet film was immersed in solution containing FA, leading to improvements in two aspects.

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All-inorganic photodetectors based on scattered CsPbBr nanoplatelets with lateral dimension as large as 10 µm are fabricated, and the CsPbBr nanoplatelets are solution processed governed by a newly developed ion-exchange soldering mechanism. Under illumination of a 442 nm laser, the photoresponsivity of photodetectors based on these scattered CsPbBr nanoplatelets is as high as 34 A W , which is the largest value reported from all-inorganic perovskite photodetectors with an external driven voltage as small as 1.5 V.

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Intrinsically high mobility and large absorption coefficient endow inorganic halide perovskites (IHPs) with great promise for high-performance photodetectors (PDs), which, however, are being hindered by the low carrier extraction and transport efficiency of the solution assembled films. Here, we report on a general strategy to enhance the perovskite film conductivity that carbon nanotubes (CNTs) conductive nanonets are constructed from to provide fast carrier tracks. Resultantly, the CsPbBr nanosheet/CNT composite films exhibit both high light harvesting and high conductivity, such advantages are demonstrated by the high performances of corresponding planar PDs.

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