نتایج جستجو برای: organometal molecules

تعداد نتایج: 193265  

Journal: :Nature communications 2014
Yuchuan Shao Zhengguo Xiao Cheng Bi Yongbo Yuan Jinsong Huang

The large photocurrent hysteresis observed in many organometal trihalide perovskite solar cells has become a major hindrance impairing the ultimate performance and stability of these devices, while its origin was unknown. Here we demonstrate the trap states on the surface and grain boundaries of the perovskite materials to be the origin of photocurrent hysteresis and that the fullerene layers d...

Journal: :The journal of physical chemistry letters 2016
Shi Liu Fan Zheng Ilya Grinberg Andrew M Rappe

Piezoelectrics play a critical role in various applications. The permanent dipole associated with the molecular cations in organometal halide perovskites (OMHPs) may lead to spontaneous polarization and thus piezoelectricity. Here we explore the piezoelectric properties of OMHPs with density functional theory. We find that the piezoelectric coefficient depends sensitively on the molecular order...

Journal: :Advanced materials 2014
Zhi-Kuang Tan Reza Saberi Moghaddam May Ling Lai Pablo Docampo Ruben Higler Felix Deschler Michael Price Aditya Sadhanala Luis M Pazos Dan Credgington Fabian Hanusch Thomas Bein Henry J Snaith Richard H Friend

Solid-state light-emitting devices based on direct-bandgap semiconductors have, over the past two decades, been utilized as energy-efficient sources of lighting. However, fabrication of these devices typically relies on expensive high-temperature and high-vacuum processes, rendering them uneconomical for use in large-area displays. Here, we report high-brightness light-emitting diodes based on ...

2016
Tomoya Hakamata Kohei Shimamura Fuyuki Shimojo Rajiv K. Kalia Aiichiro Nakano Priya Vashishta

Organometal halide perovskites are attracting great attention as promising material for solar cells because of their high power conversion efficiency. The high performance has been attributed to the existence of free charge carriers and their large diffusion lengths, but the nature of carrier transport at the atomistic level remains elusive. Here, nonadiabatic quantum molecular dynamics simulat...

Journal: :Chemical communications 2015
Hua-Rong Xia Wen-Tao Sun Lian-Mao Peng

A facile hydrothermal method was developed to prepare CH3NH3PbBr3 and CH3NH3PbI3. The as-prepared products were utilized in lithium batteries as anode materials with good performance. Considering the structural diversity, more hybrid perovskites can be targets for further optimization, indicating their promising potential in Li-ion battery applications.

2018
Yanqi Luo Sigalit Aharon Michael Stuckelberger Ernesto Magaña Barry Lai Mariana I. Bertoni Lioz Etgar David P. Fenning

Hybrid organometal halide perovskites are known for their excellent optoelectronic functionality as well as their wide-ranging chemical flexibility. The composition of hybrid perovskite devices has trended toward increasing complexity as fine-tuned properties are pursued, including multielement mixing on the constituents A and B and halide sites. However, this tunability presents potential chal...

2016
Chong Liu Jiandong Fan Hongliang Li Cuiling Zhang Yaohua Mai

Despite organometal halide perovskite solar cells have recently exhibited a significant leap in efficiency, the Sn-based perovskite solar cells still suffer from low efficiency. Here, a series homogeneous CH3NH3Pb(1-x)SnxI3 (0 ≤ x ≤ 1) perovskite thin films with full coverage were obtained via solvent engineering. In particular, the intermediate complexes of PbI2/(SnI2)∙(DMSO)x were proved to r...

2016
Xin Tong Feng Lin Jiang Wu Zhiming M. Wang

Perovskite solar cells fabricated from organometal halide light harvesters have captured significant attention due to their tremendously low device costs as well as unprecedented rapid progress on power conversion efficiency (PCE). A certified PCE of 20.1% was achieved in late 2014 following the first study of long-term stable all-solid-state perovskite solar cell with a PCE of 9.7% in 2012, sh...

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