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Wenbin Han

Bio: Wenbin Han is an academic researcher from Jilin University. The author has contributed to research in topics: Perovskite (structure) & Materials science. The author has an hindex of 7, co-authored 16 publications receiving 110 citations.

Papers
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Journal ArticleDOI
TL;DR: In this article, the influence of different doping strategies and corresponding doping mechanisms on device performance and stability was mainly discussed, and the stability issues of doped spiro-OMeTAD based PSCs were also described.
Abstract: Organic–inorganic hybrid perovskite solar cells (PSCs) have made unprecedented progress in the past ten years, the power conversion efficiency of which increased from 3.8% in 2009 to 25.5% in 2020. The choice of hole transport layers (HTLs) is a key factor for achieving efficient and stable PSCs. Recently, 2,2′,7,7′-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9′-spirobifluorene (spiro-OMeTAD) has been proven to be the most suitable small molecule HTL material in n–i–p PSCs. However, the conductivity and hole mobility of spiro-OMeTAD are dependent on the dopants. Bis(trifluoromethane)sulfonamide lithium salt (LiTFSI) and 4-tert-butylpyridine (TBP) have become the standard HTL dopants to improve the charge transport properties of n–i–p PSCs. Both of these two dopants are effective but have a negative impact on the device stability (induced by ion migration, hygroscopicity, and corrosiveness). In response, lots of efforts have been devoted to the development of alternative and new dopants. In this review, the influence of different doping strategies and corresponding doping mechanisms on device performance and stability was mainly discussed. The stability issues of doped spiro-OMeTAD based PSCs were also described. Finally, we proposed some possible future research goals for dopants based on these existing results to obtain long-lasting and high-efficiency PSCs.

111 citations

Journal ArticleDOI
TL;DR: This paper summaries recent progress regarding to modifying/remedy the drawbacks of PEDOT:PSS to improve the PCE and stability and has the potential to guide the development of PSCs based on commercial PEDot: PSS.
Abstract: Organic–inorganic hybrid perovskite solar cells (PSCs) has achieved the power conversion efficiency (PCE) of 25.2% in the last 10 years, and the PCE of inverted PSCs has reached >22%. The rapid enh...

65 citations

Journal ArticleDOI
Wenbin Han1, Guanhua Ren1, Zhiqi Li1, Minnan Dong1, Chunyu Liu1, Wenbin Guo1 
TL;DR: In this article, poly[(9,9]-dioctylfluorenyl]-2,7-diyl)-alt-co-(1,4-benzo-{2,1′,3}-thiadiazole] (PFBT) is introduced between the NiO and perovskite layers in the form of a polymer aggregate to enhance perov-skite crystallinity and decrease the interface charge recombination between perovsite and NiO in PSCs.

30 citations

Journal ArticleDOI
Zhiqi Li1, Jiaxin Guo1, Zhuowei Li1, Wenbin Han1, Guanhua Ren1, Chunyu Liu1, Liang Shen1, Wenbin Guo1 
TL;DR: In this article, a perovskite photovoltaics embedded with carbon dots has been proposed to improve the performance of perovsite solar cells by self-assembly of trichloro(3, 3, 3-trifluoropropyl)silane (C3H4Cl3F3Si) and CDs.
Abstract: Carbon dots (CDs) have significant potential in the chemical decoration, crystal modification, and surface passivation of perovskite photovoltaics. However, incompatibility between the hydrophilic/hygroscopic nature of CDs and moisture sensitive perovskite remains an issue. Solving this problem would yield a significant improvement for stable perovskite devices embedded with CDs. Herein, hydrophobic passivation layers are realized for perovskite solar cells (PSCs) through the surface engineering of CDs, exploiting electrostatic self-assembly of trichloro(3,3,3-trifluoropropyl)silane (C3H4Cl3F3Si) and CDs. The embedded CDs modify perovskite grains and passivate grain boundary defects, thereby promoting the carrier lifetime and charge collection. The inserted C3H4Cl3F3Si insulating layer provides a tunneling junction at the contact of the perovskite and electron transport layer. This tunneling layer can selectively conduct electrons and block holes, which spatially separate photo-generated carriers to suppress their recombination. As a result, the optimized perovskite devices deliver the highest efficiency of 21.12% with a high fill factor of 82.86%. Moreover, the variation of surface wettability can be achieved by the self-assembly of C3H4Cl3F3Si, which improves the stability of perovskite devices by maintaining nearly 90% efficiency for over 30 days' exposure to an ambient atmosphere without encapsulation.

23 citations

Journal ArticleDOI
Zhiqi Li1, Chunyu Liu1, Xinyuan Zhang1, Guanhua Ren1, Wenbin Han1, Wenbin Guo1 
01 Jan 2019-Small
TL;DR: A simple strategy to improve the efficiency and stability of perovskite photovoltaic devices using low-cost carbon nanomaterials using 1D N-type doped carbon nanorods.
Abstract: To overcome the zigzag pathway transport of the electron diffusion process and eliminate the surface trap states of phenyl-C61-butyric acid methyl ester (PCBM) nanofilms in inverted perovskite solar cells, novel 1D N-type doped carbon nanorods (CNRs) are developed by a stibonium (Sb) auxiliary ball milling method and introduced into the PCBM film to prepare the PCBM:Sb-CNRs hybrid transport layer. In this way, the N-type doped Sb-CNRs can extend the built-in electric field between CH3 NH3 PbI3 and PCBM to facilitate the separation of electron/hole pairs. The discontinuous band with the built-in potential in the PCBM/Sb-CNRs heterojunction can boost interfacial charge redistribution and promote electrons diffusion from PCBM to electrode through 1D Sb-CNRs network. As a result, the high device efficiency of 19.26% with enhanced air stability and little hysteresis are achieved. This work demonstrates a simple strategy to improve the efficiency and stability of perovskite photovoltaic devices using low-cost carbon nanomaterials.

20 citations


Cited by
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TL;DR: In this paper, the authors summarized and discussed recent advances in passivation engineering for perovskite film formation or interface optimization, and predicted future research trends concerning passivation in advancing the development of PSCs, especially in efficiency, stability, and commercialization.

78 citations

Journal ArticleDOI
TL;DR: In this article, a simple, inexpensive and effective interfacial engineering strategy was developed by doping PEDOT:PSS with cesium iodide (CsI) to reduce the voltage loss and achieve highly efficient inverted PSCs.
Abstract: PEDOT:PSS is widely used in perovskite solar cells (PSCs) as the most popular hole transporting layer (HTL). However, p-i-n type inverted planar PSCs based on the PEDOT:PSS HTL typically exhibit up to 200 mV more voltage loss compared to conventional planar PSCs (n-i-p) that generally show open circuit voltages (VOC) of around 1.1 V. In this study, we develop a simple, inexpensive and effective interfacial engineering strategy by doping PEDOT:PSS with cesium iodide (CsI) to reduce the voltage loss and achieve highly efficient inverted PSCs. SEM, AFM, and XPS measurements suggest that CsI modifies the interface between PEDOT:PSS and perovskite by reacting with PbI2 to form CsPbI3, thus facilitating interfacial contact and charge transport. Moreover, after CsI-modification (CsI-PEDOT:PSS), the hole transport properties of PEDOT:PSS and the hole extraction are enhanced, while the energy levels are more favorable and charge recombination is suppressed. Importantly, compared to pristine PEDOT:PSS that suffers from a large non-radiative recombination loss (0.375 V), CsI-PEDOT:PSS makes the device to realize an impressively low non-radiative voltage loss (only 0.287 V). As a result, inverted PSCs based on CsI-PEDOT:PSS show a small voltage loss, an excellent power conversion efficiency (PCE) of 20.22%, and no hysteresis and achieve a high VOC (1.084 V), while the control device without CsI shows an inferior efficiency of 16.57%. Both the high VOC and PCE are an improvement over literature data on modified PEDOT:PSS-based inverted PSCs.

65 citations