Huaigang Su
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Huaigang Su has a total of 35 co-authors. Here are the top co-authors by number of shared publications:
- Wenjing Lou
Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences
5 shared publications - Yanxing Qi
State Key Laboratory for Oxo Synthesis & Selective Oxidation
3 shared publications - Cheng Jiang
State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, No. 18 Tianshui Middle Road, Lanzhou 730000, China
2 shared publications - Qian Jia
State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, No. 18 Tianshui Middle Road, Lanzhou 730000, China
2 shared publications - Qilong Zhao
State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, No. 18 Tianshui Middle Road, Lanzhou 730000, China
2 shared publications - Qin Zhao
State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, China
2 shared publications
Latest Publications
- Open Access
- 9 May 2026
- Published by Springer Nature in Nature Communications
- Vol. 17 (1)
Highly efficient and stable perovskite photovoltaics enabled by multifunctional crosslinked n+-type interlayer
Tin dioxide (SnO2) stands as a premier electron transport layer in n-i-p perovskite solar cells (PSCs), yet interfacial defect-induced carrier recombination and energy-level misalignment impede its commercialization. Herein, we engineer a multifunctional polymeric interlayer by introducing polymerizable dimethyldiallylammonium chloride (DADMAC) at the SnO2/perovskite interface. The densely cross-linked P-DADMAC network reinforces mechanical interlocking, enhancing interfacial adhesion and stress dissipation. Concurrently, chloride ions (Cl⁻) from P-DADMAC synergistically passivate defects at both the perovskite buried interface and SnO2 surface, inducing a graded n+-type band bending. This energy-band engineering reduces the heterojunction energy-level offset by 0.24 eV, thereby facilitating efficient charge extraction and minimizing non-radiative losses. Consequently, n-i-p devices achieve a power conversion efficiency (PCE) of 26.34% with a fill factor (FF) of 85.84% (certified: 26.27%), while a 25 cm2 module (active area: 14 cm2) attains 22.03% PCE (FF > 80%). This work establishes a paradigm for interfacial multifunctionalization in high-performance photovoltaics.
- 9 May 2026
- Published by Springer Nature in Nature Communications
- Vol. 17 (1)
Open AccessHighly efficient and stable perovskite photovoltaics enabled by multifunctional crosslinked n+-type interlayer
Tin dioxide (SnO2) stands as a premier electron transport layer in n-i-p perovskite solar cells (PSCs), yet interfacial defect-induced carrier recombination and energy-level misalignment impede its commercialization. Herein, we engineer a multifunctional polymeric interlayer by introducing polymerizable dimethyldiallylammonium chloride (DADMAC) at the SnO2/perovskite interface. The densely cross-linked P-DADMAC network reinforces mechanical interlocking, enhancing interfacial adhesion and stress dissipation. Concurrently, chloride ions (Cl⁻) from P-DADMAC synergistically passivate defects at both the perovskite buried interface and SnO2 surface, inducing a graded n+-type band bending. This energy-band engineering reduces the heterojunction energy-level offset by 0.24 eV, thereby facilitating efficient charge extraction and minimizing non-radiative losses. Consequently, n-i-p devices achieve a power conversion efficiency (PCE) of 26.34% with a fill factor (FF) of 85.84% (certified: 26.27%), while a 25 cm2 module (active area: 14 cm2) attains 22.03% PCE (FF > 80%). This work establishes a paradigm for interfacial multifunctionalization in high-performance photovoltaics.
- Open Access
- 22 January 2025
- Published by MDPI AG in Lubricants
- Vol. 13 (2) , 45
Catalytic and Tribological Performances of a Novel Bi-Functional Ionic Liquid in Lubricating Ester Oil
To address the detrimental effects of the residue of catalysts on the tribological performances of ester lubricants, a novel and efficient bi-functional ionic liquid 1-(3,5-di-tert-butyl-4-hydroxybenzyl)-3-methylimidazole di(2-ethylhexyl) phosphate ([(BHT-1)MIM][DEHP]) was prepared. The catalyst not only facilitates the synthesis of pentaerythritol tetra-hexanoate (PETH) through the catalytic esterification reaction—achieving up to 96% conversion with a 94% yield—but also enhances the tribological performance of ester oil PETH when used as a lubricant additive. The tribological property has been improved remarkably: the mean friction coefficient for PETH + [(BHT-1)MIM][DEHP] is notably lower, at 0.110, compared to the PETH, which has a coefficient of 0.180. Meanwhile, the wear scar diameter of the steel ball, when lubricated with PETH + [(BHT-1)MIM][DEHP], is notably smaller than that of a steel ball lubricated solely with PETH. Especially, the reduction in the wear volume at 100 °C is up to 81.46% compared with the base oil PETH. [(BHT-1)MIM][DEHP], PETH + [(BHT-1)MIM][DEHP], and the worn track of the upper running ball and lower disc were systematically characterized by using Nuclear Magnetic Resonance (NMR) spectra, a Fourier Transform Infrared Spectrometer (FT-IR), a field emission scanning electron microscope (FESEM), Thermal gravity analysis (TG), X-ray photoelectron spectroscopy (XPS), and an optical microscope (OM). The wear mechanism of the tailored lubricant oil was discussed in terms of the chemical composition of the worn surface.
- 22 January 2025
- Published by MDPI AG in Lubricants
- Vol. 13 (2) , 45
Open AccessCatalytic and Tribological Performances of a Novel Bi-Functional Ionic Liquid in Lubricating Ester Oil
To address the detrimental effects of the residue of catalysts on the tribological performances of ester lubricants, a novel and efficient bi-functional ionic liquid 1-(3,5-di-tert-butyl-4-hydroxybenzyl)-3-methylimidazole di(2-ethylhexyl) phosphate ([(BHT-1)MIM][DEHP]) was prepared. The catalyst not only facilitates the synthesis of pentaerythritol tetra-hexanoate (PETH) through the catalytic esterification reaction—achieving up to 96% conversion with a 94% yield—but also enhances the tribological performance of ester oil PETH when used as a lubricant additive. The tribological property has been improved remarkably: the mean friction coefficient for PETH + [(BHT-1)MIM][DEHP] is notably lower, at 0.110, compared to the PETH, which has a coefficient of 0.180. Meanwhile, the wear scar diameter of the steel ball, when lubricated with PETH + [(BHT-1)MIM][DEHP], is notably smaller than that of a steel ball lubricated solely with PETH. Especially, the reduction in the wear volume at 100 °C is up to 81.46% compared with the base oil PETH. [(BHT-1)MIM][DEHP], PETH + [(BHT-1)MIM][DEHP], and the worn track of the upper running ball and lower disc were systematically characterized by using Nuclear Magnetic Resonance (NMR) spectra, a Fourier Transform Infrared Spectrometer (FT-IR), a field emission scanning electron microscope (FESEM), Thermal gravity analysis (TG), X-ray photoelectron spectroscopy (XPS), and an optical microscope (OM). The wear mechanism of the tailored lubricant oil was discussed in terms of the chemical composition of the worn surface.
- Open Access
- 1 January 2025
- Published by SCIE Publishing Limited in Green Chemical Technology
- Vol. 2 (4) , 10016
A Green Way for the Synthesis of Ester Oil by an Ionic Liquid as Both a Catalyst and Lubricant Additive
SCIEPublish is an international open-access journal publishing service provider run by SCIE Publishing Limited, dedicated to supporting and inspiring scientists or institutions/societies who aspire to publish high-quality journals.
- 1 January 2025
- Published by SCIE Publishing Limited in Green Chemical Technology
- Vol. 2 (4) , 10016
Open AccessA Green Way for the Synthesis of Ester Oil by an Ionic Liquid as Both a Catalyst and Lubricant Additive
SCIEPublish is an international open-access journal publishing service provider run by SCIE Publishing Limited, dedicated to supporting and inspiring scientists or institutions/societies who aspire to publish high-quality journals.
- Open Access
An Efficient Zr-ZSM-5-st Solid Acid Catalyst for the Polyol Esterification Reaction
In this study, Zr active species were implanted into a ZSM-5 zeolite framework to form a solid acid catalyst through steam treatment and the liquid-solid isomorphous substitution process. The as-synthesized Zr-ZSM-5-st catalyst ensured excellent esterification of trimethylolpropane and fatty acids (FAs) to achieve a polyol ester production yield of 94.41%. Combined with N2 physisorption, X-ray diffraction, Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, transmission electron microscopy mapping, X-ray photoelectron spectroscopy, NH3 temperature-programmed desorption, and inductively coupled mass plasma spectroscopy were conducted. The results revealed that the excellent performance of Zr-ZSM-5-st catalyst could be attributed to the enhanced acidity and the developed surface area and pore structure.
Open AccessAn Efficient Zr-ZSM-5-st Solid Acid Catalyst for the Polyol Esterification Reaction
In this study, Zr active species were implanted into a ZSM-5 zeolite framework to form a solid acid catalyst through steam treatment and the liquid-solid isomorphous substitution process. The as-synthesized Zr-ZSM-5-st catalyst ensured excellent esterification of trimethylolpropane and fatty acids (FAs) to achieve a polyol ester production yield of 94.41%. Combined with N2 physisorption, X-ray diffraction, Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, transmission electron microscopy mapping, X-ray photoelectron spectroscopy, NH3 temperature-programmed desorption, and inductively coupled mass plasma spectroscopy were conducted. The results revealed that the excellent performance of Zr-ZSM-5-st catalyst could be attributed to the enhanced acidity and the developed surface area and pore structure.
- Open Access
- 10 May 2022
- Published by MDPI AG in Lubricants
- Vol. 10 (5) , 91
Influence of Additive Chemistry on the Tribological Behavior of Steel/Copper Friction Pairs
Tribological properties of five anti-wear additives for a steel-copper contact were investigated. It was found that the tribological performances are closely related to the molecular structure of additives. The protic ionic liquid anti-wear additive AW316 exhibits the best tribological performance with the lowest mean friction coefficient of 0.082, and the smallest wear volume, which is more than one order of magnitude smaller than base oil. Transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS) tests reveal that a 10–15 nm thickness uniform boundary lubrication film composed of oxides, phosphates, and cuprous oxide was formed on the copper disc, which was responsible for its outstanding tribological performances.
- 10 May 2022
- Published by MDPI AG in Lubricants
- Vol. 10 (5) , 91
Open AccessInfluence of Additive Chemistry on the Tribological Behavior of Steel/Copper Friction Pairs
Tribological properties of five anti-wear additives for a steel-copper contact were investigated. It was found that the tribological performances are closely related to the molecular structure of additives. The protic ionic liquid anti-wear additive AW316 exhibits the best tribological performance with the lowest mean friction coefficient of 0.082, and the smallest wear volume, which is more than one order of magnitude smaller than base oil. Transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS) tests reveal that a 10–15 nm thickness uniform boundary lubrication film composed of oxides, phosphates, and cuprous oxide was formed on the copper disc, which was responsible for its outstanding tribological performances.
- 6 December 2021
- Published by Wiley in Lubrication Science
- Vol. 34 (2) , 84-92
Nanosized molybdenum disulfide on surface‐modified carbon material as lubricating oil additive for friction‐reduction and anti‐wear
For the first time, nanosized molybdenum disulfide (MoS2) nanoparticles (NPs) were grown on the surface of poly(ethylene glycol)‐polydopamine‐modified reduction graphene oxide) nanosheets (rGO‐PDA‐PEG). The obtained rGO‐PDA‐PEG@MoS2 nanocomposites exhibits excellent dispersion in polyalkylene glycol (PAG) synthetic oil and outperforms GO and MoS2 NPs as additives in terms of friction reduction and wear resistance at elevated temperature. The superior tribological behaviour of rGO‐PDA‐PEG@MoS2 might be beneficial to the synergistic effect between MoS2 and rGO.
- 6 December 2021
- Published by Wiley in Lubrication Science
- Vol. 34 (2) , 84-92
Nanosized molybdenum disulfide on surface‐modified carbon material as lubricating oil additive for friction‐reduction and anti‐wear
For the first time, nanosized molybdenum disulfide (MoS2) nanoparticles (NPs) were grown on the surface of poly(ethylene glycol)‐polydopamine‐modified reduction graphene oxide) nanosheets (rGO‐PDA‐PEG). The obtained rGO‐PDA‐PEG@MoS2 nanocomposites exhibits excellent dispersion in polyalkylene glycol (PAG) synthetic oil and outperforms GO and MoS2 NPs as additives in terms of friction reduction and wear resistance at elevated temperature. The superior tribological behaviour of rGO‐PDA‐PEG@MoS2 might be beneficial to the synergistic effect between MoS2 and rGO.
- 14 August 2021
- Published by Springer Nature in Catalysis Letters
- Vol. 152 (6) , 1801-1818
Simple Thermocatalytic Oxidation Degradation of VOCs
- 14 August 2021
- Published by Springer Nature in Catalysis Letters
- Vol. 152 (6) , 1801-1818
Simple Thermocatalytic Oxidation Degradation of VOCs