Hongli Gao

Dr. Hongli Gao

Faculty of Science, Beijing University of Technology, Beijing, 100124, China

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 May 2024 in Molecules
Verified
Journal Article
Open access
PDF file
ZWZhanwei Wang
Zhanwei Wang
Hongli GaoHongli Gao
Hongli Gao
DWDandan Wu
Dandan Wu
JMJunhua Meng
Junhua Meng
JDJinxiang Deng
Jinxiang Deng
MCMin Cui
Min Cui
Perovskite solar cells have made significant strides in recent years. However, there are still challenges in terms of photoelectric conversion efficiency and long-term stability associated with perovskite solar cells. The presence of defects in perovskite materials is one of the important influencing factors leading to subpar film quality. Adopting additives to passivate defects within perovskite materials is an effective approach. Therefore, we first discuss the types of defects that occur in perovskite materials and the mechanisms of their effect on performance. Then, several types of additives used in perovskite solar cells are discussed, including ionic compounds, organic molecules, polymers, etc. This review provides guidance for the future development of more sustainable and effective additives to improve the performance of solar cells.

1 July 2021 in Vacuum
Verified
Journal Article
Closed access
YJYujia Jiao
Yujia Jiao
QJQian Jiang
Qian Jiang
JMJunhua Meng
Junhua Meng
JZJinliang Zhao
Jinliang Zhao
ZYZhigang Yin
Zhigang Yin
XZXingwang Zhang
Xingwang Zhang

16 March 2021 in Nanoscale
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Journal Article
Closed access
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LJLei Jin
Lei Jin
LWLirong Wang
Lirong Wang
Xiaoming ZhangXiaoming Zhang
Xiaoming Zhang
YLYing Liu
Ying Liu
XDXuefang Dai
Xuefang Dai
GLGuodong Liu
Guodong Liu
A YN2 monolayer can realize multiple topological phases, determined based on the magnetization direction. In particular, the in-plane QAHE can be realized in a d0 ferromagnet.

23 May 2020 in Journal of Materials Science: Materials in Electronics
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Journal Article
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Hongli GaoHongli Gao
Hongli Gao
JMJunhua Meng
Junhua Meng
JSJunjie Sun
Junjie Sun
JDJinxiang Deng
Jinxiang Deng

18 October 2021 in Journal of Materials Chemistry C
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Journal Article
Closed access
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WMWeizhen Meng
Weizhen Meng
Xiaoming ZhangXiaoming Zhang
Xiaoming Zhang
YLYing Liu
Ying Liu
XDXuefang Dai
Xuefang Dai
Hongli GaoHongli Gao
Hongli Gao
GLGuodong Liu
Guodong Liu
Electrides in two-dimensional (2D) scale, especially those capture inherent magnetism and low work functions, have shown great application prospects in nanoscale spintronic devices and electronic emitters. However, searching ideal 2D magnetic electrides are still great challenges. Herein, based on first-principles calculations, we demonstrate 2D CaCl is strippable from the heterostructure of experimental CaCl/graphene and reveal the freestanding 2D CaCl is a novel electride phase. In this material, sufficient electrons are trapped in the lattice voids and act as anions within the positive crystalline framework, following the electide form of [CaCl]+●e-. Due to the unique electron behaviours of electrides, 2D [CaCl]+●e- possesses a series of interesting physical phenomena. 1) The electride [CaCl]+●e- exhibits room-temperature ferromagnetism, the magnetic moment originates from the excess electrons with s-like orbital feature rather than atomic orbital ones, which is drastically different with traditional 2D ferromagnets. 2) The electride [CaCl]+●e- shows magnetic metal characteristics, and by doping halogen elements can exectively regulate the electronic structure. 3) Most remarkably, FM electride [CaCl]+●e- shows an extremely low work function (2.65 eV). This value is the lowest among electrides in 2D materials reported so far. Besides, the dimension of excess electron can be effectively regulated by controlling temperature. This work provides an excellent candidate to investigate 2D magnetic electrides and associated applications.

18 April 2012 in Journal of Physics D: Applied Physics
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Journal Article
Closed access
Hongli GaoHongli Gao
Hongli Gao
Tiejun ZhuTiejun Zhu
Tiejun Zhu
HWH Wang
H Wang
ZRZhifeng Ren
Zhifeng Ren
XZX B Zhao
X B Zhao
The effect of Pb in La3Te4−x Pb x on the thermoelectric properties in the temperature range 300–1100 K was studied on samples synthesized by the melting, ball milling and hot-pressing method. The samples crystallize in the Th3P4structure. A small amount of Pb substitution for Te in La3Te4 reduced the electrical conductivity, but the impurity phase introduced by more Pb significantly enhanced the electrical conductivity. The electrical conductivity of the La3Te3.6Pb0.4 sample reached 2.06 × 105 S m−1 at room temperature. The expansion of crystal lattice confirmed from x-ray diffraction patterns and the slight reduction in electrical conductivity all verify the fact that Pb substitutes a Te site when x is small. The Seebeck coefficient increases linearly with temperature for all samples. While the thermal conductivity varies slightly with temperature, the lattice thermal conductivity approaches the minimum value at high temperatures. For La3Te3.7Pb0.3, a power factor of 1.4 × 10−3 W m−1 K−2 at 1100 K was achieved with a thermal conductivity of 1.86 W m−1 K−1, giving a maximum figure-of-merit ZT ≈ 0.8 at 1100 K.