Nano Research
·
2018
·Vol. 11
·期 9
·4587-4598
·
IF 7.994
Zhang Jingtong,Chen Yalan,Liu Ming,Du Kun,Zhou Yan,Li Yanpeng,Wang Zhaojie,Zhang Jun
Few-layered MoSe 2 nanosheets with mixed 1T/2H phase were successfully arrayed on a Ti substrate (forming 1T@2H-MoSe 2 /Ti) through a facile one-step solvothermal process. After testing different synthesis conditions, it was found that the optimal process involves a temperature of 200 °C and a reaction time of 12 h. Structural characterizations reveal that the morphology of 1T@2H-MoSe 2 consists of edge-terminated nanosheets with one to five layers, composed of a mixed 1T/2H phase dominated by the 1T one. The 1T@2H-MoSe 2 /Ti electrode shows excellent HER catalytic activity, with a small onset potential (−120 mV vs. reversible hydrogen electrode, RHE) and an electrode potential of only −133 mV (vs. RHE) to achieve a current density of 20 mA·cm −2 . This excellent electrocatalytic activity is due to the synergistic effects of 1T metallic phase, few-layered nanosheet morphology, and direct growth of 1T@2H-MoSe 2 on the Ti substrate. In addition, the 1T@2H-MoSe 2 /Ti electrode shows excellent stability towards long-term electrolysis. This is due to the long-term stability of the valence states of Mo and Se, as shown by post-electrolysis X-ray photoelectron spectroscopy analysis.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2020
·
IF 6.182
Yi Wang,Xinyan Xiao,Jiayi Chen,Mingli Lu,Xingye Zeng
An ordered 1T/2H MoSe 2 possessed few-layers nanosheets structure was synthesized by a NaBH 4 -assisted hydrothermal method. Further, 1T/2H MoSe 2 was integrated with proton g-C 3 N 4 via solvothermal method, forming a novel 2D/2D heterostructure composite (1T/2H MoSe 2 /pg-C 3 N 4 ) with Z-scheme heterojunction. 1T/2H MoSe 2 /pg-C 3 N 4 had narrower bandgap, abundant active sites, as well as better photocurrent response and conductivity, confirmed by spectroscopic and electrochemical characterizations. Consequently, the optimal 1T/2H MoSe 2 /pg-C 3 N 4 at 1 wt% MoSe 2 loading showed enhanced TC (RhB) photodegrading rate of 92% (99%), within 80 min (45 min) of simulated solar light irradiation, being 3.0 (3.4) and 1.2 (1.2) times than that of pg-C 3 N 4 and 2H MoSe 2 /pg-C 3 N 4 , respectively. Additionally, active species trapping experiments indicated that O 2 − and h + were the main species of contaminants degradation over 1T/2H MoSe 2 /pg-C 3 N 4 . Combining with DRS, Mott-Schottky and VB XPS analysis, a reasonable 1T phase boosted Z-scheme MoSe 2 -based heterojunction mechanism was proposed.
研究领域:
材料科学
·
环境科学
·
光催化
✓ 已验证
DOI
高影响因子
ACS Applied Nano Materials
·
2025
·
IF 5.5
Tengfei Wang,Qing Pang,Boyu Liu,Hongyu Wang
In recent years, molybdenum diselenide (MoSe2) nanomaterials have been proven to be promising electromagnetic wave (EMW) absorbers, attributed to the formation of a heterogeneous interface between the 2H semiconductor phase and the 1T metal phase during its preparation. However, the difficulty in precisely controlling the two-phase ratio and the complexity of the process hinder its further development. In this work, we constructed a simple phase engineering strategy based on the regulation of reducing agent concentration, achieving a regulation of the 1T phase proportion in defective 1T/2H-MoSe2 nanomaterials (ranging from 67.91 to 41.45%) by accurately adjusting the amount of NaBH4 added. The findings indicate that the material exhibits excellent microwave absorption performance when the 1T phase proportion reaches 53.55% (1T/2H-MoSe2-2), demonstrating a minimum reflection loss (RLmin) of −40.0 dB, and the effective absorption bandwidth (EAB) covers 6.08 GHz (11.92–18.0 GHz) when the thickness is 2.6 mm. The enhancement in performance results from a synergistic balance mechanism established by the abundant 1T-2H heterogeneous interface, which induces interfacial polarization loss, along with a moderately enhanced conductive loss in the 1T/2H-MoSe2-2 nanomaterial. Furthermore, radar cross-section (RCS) simulation results confirm the dramatic dissipation ability of absorbers for EMW in practical applications. This strategy paves the way for designs of interfaces and the control of the performance of absorbing nanomaterials based on transition-metal dichalcogenides (TMDs).
研究领域:
材料科学
·
电磁学
✓ 已验证
产品关联
DOI
高影响因子
MATERIALS CHEMISTRY AND PHYSICS
·
2021
·
IF 4.094
Yinggang Liu,Shuai Liu,Hanxiao Li,Lijun Yu,Lan Sun,Jiale Xue,Ruojun Xu,Guoxiang Chen
Transition metal dichalcogenides (TMDCs) are considered as the potential electrocatalysts for hydrogen evolution reaction (HER) owing to the two-dimensional (2D) geometry and tunable band gap. However, both the inefficient electron transferring and high Gibbs free energies for hydrogen adsorption (ΔG H *) in MoSe 2 limit its further improvement in catalytic performance. Herein, the few-layered 1T@2H–MoSe 2 composite nanosheets are synthesized by one-pot hydrothermal reaction . It is found that the morphology and composites of nanosheets could be influenced by hydrothermal reaction parameters. As compared to pure 2H–MoSe 2 , 1T@2H–MoSe 2 electrode exhibits remarkable activity for HER with a low overpotential (118 mV), small Tafel slope (65.8 mV·dec −1 ) as well as large electrochemical active area (C dl = 37.5 mF cm −2 ) in acid electrolytes. Density functional theory (DFT) calculations demonstrate that ΔG H * of 1T@2H–MoSe 2 (0.232 eV) is much lower than these of pure 1T-MoSe 2 and 2H–MoSe 2 . It could be ascribed to both the optimized charge transfer and increased density of active sites in 1T@2H–MoSe 2 nanosheets.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2020
·
IF 6.182
Zhuangzhi Wu,Rongbin Zhang,Hao Fei,Ruoqi Liu,Dezhi Wang,Xinli Liu
The NH 3 is generally synthesized by the traditional Haber–Bosch method, which is energy-consuming and releases a lot of CO 2 . Electrocatalytic fixation of N 2 is highlighted as a carbon-free route to generate NH 3 by the nitrogen reduction reaction (NRR), but strongly demands highly efficient and durable electrocatalysts. Herein, we propose the multiphasic 1T@2H-MoSe 2 as a highly active NRR catalyst for the first time, which exhibits excellent activity for the NRR with a NH 3 yield of 19.91 ± 0.89 μg h −1 mg cat . −1 and a FE of 2.82% ± 0.1% at −0.6 V in 0.1 M Na 2 SO 4 . Moreover, a good durability is also demonstrated.
研究领域:
材料科学
·
化学工程
·
催化科学
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 48
·期 3
·1372-1380
·
IF 3.3
Peng Sun,Menglu Zhang,Yue Liu,Jiahua Zhao,Jiawei Yang,Yufeng Wang,Yongfei Wang,Zhiqiang Zhang
Lithium-ion batteries have been regarded as a promising power source for various electronic devices. Compared to the traditional graphite anode material, MoSe2 possesses a higher theoretical capacity. However, MoSe2 anode materials are limited by low electronic conductivity and large volume changes during cycling. This study reports 1T–2H MoSe2/N-doped rGO nanocomposites, fabricated through a hydrothermal method. The 1T–2H MoSe2/N-doped rGO electrode delivers a high reversible capacity of 483.6 mA h g−1 after 1000 cycles at 1000 mA g−1. It also possesses a high reversible capacity of 474.9 mA h g−1 even at a current density of 2000 mA g−1, thus, making it an important potential lithium-ion battery anode.
研究领域:
材料科学
·
能源存储技术
✓ 已验证
产品关联
DOI
高影响因子
Inorganic Chemistry Frontiers
·
2024
·
IF 6.1
Zhiqi Li,Jiawen Yan,Qiming Li,Ao Xu,Jianchao Sun,Yijing Wang,Xiaoyu Zhang,Xueqin Sun,Fuyi Jiang,Yanli Zhou
MoSe2 with a two-dimensional layer-like structure has been considered a promising anode material for sodium-ion batteries (SIBs) on account of its high capacity and rich reserves on Earth. However, the inherent low conductivity of 2H-MoSe2, as well as the inevitable volume fluctuation during cycling, causes structural collapse and capacity decline, resulting in poor rate capability and unacceptable cycling stability. To improve the sodium storage properties of 2H-MoSe2, the Te doping strategy has been adopted to successfully synthesize Te doped 1T/2H-MoSe2 nanosheets (Te-MoSe2) via a facile two-step reaction. The Te doping induces the phase transition of 2H-MoSe2 to form 1T-MoSe2, which can improve the electron conductivity and generate more active sites, benefiting the promotion of sodium storage capacity. Besides, the 1T/2H heterogeneous interface accelerates the charge transfer kinetics. Thus, as an innovative anode material for sodium-ion half batteries, Te-MoSe2 exhibits better sodium storage performances than pure MoSe2. The full batteries composed of the Te-MoSe2 anode and Na3V2(PO4)3@rGO cathode also deliver remarkable electrochemical performances. The related kinetics results confirm the excellent electron transfer efficiency and rapid Na+ diffusion behavior of Te-MoSe2. Moreover, the reaction mechanism has also been elucidated by some ex situ characterization techniques. The good reversibility and excellent sodium storage properties of the Te-MoSe2 electrode indicate its potential application in future energy storage fields.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Yi Wang,Xinyan Xiao,Tingting Ding,Mingli Lu
The transition-metal dichalcogenides (TMDs) with 1T phase structure holds great promise for providing abundant active sites and superior conductivity, while the achievement of highly efficient degradation activity over bare TMDs and TMDs-based photocatalysts is still challenges. In this work, a flower-like mixed 1T-2H phase MoSe 2 was synthesized via a sodium borohydride (NaBH 4 )-assisted solvothermal method, and then was selected as a “charge-transfer-bridge” to fabricate a dual Z-scheme AgI/1T-2H MoSe 2 /Bi 4 O 5 Br 2 composite with a 0D/3D hierarchical structure. The optimal AgI/1T-2H MoSe 2 /Bi 4 O 5 Br 2 composite exhibited the superior photocatalytic activity towards degrading RhB and TC relative to AgI/2H MoSe 2 /Bi 4 O 5 Br 2 and AgI/Bi 4 O 5 Br 2 . The enhancement is attributed to its better light absorption, abundant active sites, and superior charge carrier mobility and separation efficiency, resulted from synergetic effect of 0D/3D structural coupling and energy band matching. Moreover, the important energy band alignments and mixed 1T-2H phase MoSe 2 boosting photocatalytic mechanism of as-prepared AgI/1T-2H MoSe 2 /Bi 4 O 5 Br 2 heterojunction were investigated. This work describes a competitive design and fabrication technique for constructing novel mixed phase TMDs-based Z-scheme heterojunctions to address environmental issues.
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）