Pt-like catalytic behavior of MoNi decorated CoMoO3 cuboid arrays for the hydrogen evolution reaction

2018 ◽  
Vol 6 (32) ◽  
pp. 15558-15563 ◽  
Author(s):  
Dewen Wang ◽  
Ce Han ◽  
Zhicai Xing ◽  
Qun Li ◽  
Xiurong Yang

Owing to the unique structure and synergistic effect between MoNi and CoMoO3, the MoNi/CoMoO3/NF exhibits high hydrogen evolution activity which requires a low overpotential of only 18 mV to deliver a current density of 10 mA cm−2.

2020 ◽  
Vol 56 (56) ◽  
pp. 7702-7705 ◽  
Author(s):  
Lei Guo ◽  
Xue Bai ◽  
Hui Xue ◽  
Jing Sun ◽  
Tianshan Song ◽  
...  

A 3D hierarchical Bi-doped CoP nanoflowers electrocatalyst is developed based on a MOF self-sacrifice strategy. The 3% Bi/CoP catalyst delivers a current density of 10 mA cm−2 at low overpotentials of 122 mV in alkaline electrolyte and 150 mV in acidic electrolyte.


2017 ◽  
Vol 5 (16) ◽  
pp. 7564-7570 ◽  
Author(s):  
Peili Zhang ◽  
Hong Chen ◽  
Mei Wang ◽  
Yong Yang ◽  
Jian Jiang ◽  
...  

A hierarchically structured Ni–Co–P film exhibits remarkable activity toward the hydrogen evolution reaction with a current density of −10 mA cm−2 at −30 mV vs. the RHE.


2019 ◽  
Vol 3 (10) ◽  
pp. 2771-2778 ◽  
Author(s):  
Shancheng Yan ◽  
Ka Wang ◽  
Qingxia Wu ◽  
Fei Zhou ◽  
Zixia Lin ◽  
...  

The ultrafine Co:ZnS/CoS2 heterostructure nanowires with high hydrogen evolution performance by one-step hydrothermal method. The overpotential required to reach a current density of 10 mAcm−2 was only 78 mV in 0.5 M H2SO4 solution, and the Tafel slope was 56 mV dec−1.


RSC Advances ◽  
2015 ◽  
Vol 5 (110) ◽  
pp. 90265-90271 ◽  
Author(s):  
Lili Li ◽  
Xingyue Li ◽  
Lunhong Ai ◽  
Jing Jiang

Zeolitic imidazolate framework-67 derived nanostructured CoP assemblies exhibited high-performance for electrochemical HER, as manifested by a low overpotential, a large cathodic current density and an excellent durability.


2018 ◽  
Vol 15 (2) ◽  
pp. 178-187
Author(s):  
Lixin Wang ◽  
Peipei Zhang ◽  
Lei Bai ◽  
Lei Cao ◽  
Jing Du ◽  
...  

Background: Ni/rGO composite electrode has been fabricated by facile supergravity electrodeposition as a low-cost catalyst for efficient hydrogen evolution in alkaline media. In this paper, the electrodeposition time is the main research variable. When the electrodeposition time is 100 minutes, the Ni/rGO-100 catalyst manifests the highest electrocatalytic activity toward the hydrogen evolution reaction (HER). In 1.0 M NaOH solution, the overpotential at a current density of 100 mA cm-2, Tafel slope and charge transfer resistance of Ni/rGO-100 catalyst is 184 mV, 77 mV dec-1 and 4.173 Ω, respectively. In addition, Ni/rGO-100 catalyst shows a long-term durability at a constant current density of 100 mA cm-2 for 10 h. The outstanding HER electrocatalytic performance of the Ni/rGO-100 is mainly related to the synergetic combination of Ni and rGO, as well as the enlarged exposure of catalytically active sites and improved transport of electrons arising from the good conductivity of graphene. Method: In a classic experiment, GO was prepared by modified Hummers method. The Ni/rGO composite electrodes were prepared by supergravity electrodeposition, which has been reported in detail in our published paper. Firstly, a ø10 cm × 2 cm Ni foam circle was cleaned sequentially in HCl solution (15%), acetone and DI water for 5 min with ultrasonication to be used as a cathode. And a pure nickel pipe was used as anode. The Ni/rGO composite cathodes were electrodeposited in a blackish green plating bath which contained 350 g L-1 Ni(NH2SO3)2·6H2O, 10g L-1 NiCl2·6H2O, 30 g L-1 NH4Cl , 1.0 g L-1 GO colloidal solution with different electrodeposition time, 10min, 30min, 60min, 80min, 100min, respectively. The pH value of the plating bath is 3.5-3.8. The above five electrodes were respectively denominated as Ni/rGO-10, Ni/rGO-30, Ni/rGO-60, Ni/rGO-80, Ni/rGO-100. All composite electrodes were performed under the strength of the supergravity with G=350 g at a current density of 3 A dm-2 at 318 K. Afterwards the Ni foam coated with Ni/rGO hybrid was taken out of the reaction vessel, followed by washing with deionized water to remove physical adsorption residua, and then dried at 80°C. Results: In this paper, the electrodeposition time is the main research variable. When the electrodeposition time is 100 minutes, the Ni/rGO-100 catalyst manifests the highest electrocatalytic activity toward the hydrogen evolution reaction (HER). In 1.0 M NaOH solution, the overpotential at a current density of 100 mA cm-2, Tafel slope and charge transfer resistance of Ni/rGO-100 catalyst is 184 mV, 77 mV dec-1 and 4.173 Ω, respectively. In summary, we have synthesized a class of composite electrodes (Ni/rGO) for HER in alkaline solution by electrodeposition under supergravity field. We studied the effect of electrodeposition time on electrode performance in detail. With the increase of electrodeposition time, the number of active sites is enlarged provided by the electrode. When the electrodeposition time is 100 min, we fabricate the best electrode (Ni/rGO-100). The η100, Tafel slope and charge transfer resistance of Ni/rGO-100 is 184 mV, 77 mV dec-1 and 4.173 Ω, respectively. The introduction of graphene and supergravity field plays a key role in improving the performance of the electrodes. This work is a pivotal part of the development of Ni/rGO as a non-precious HER catalyst for green energy field.


2021 ◽  
Vol 50 (39) ◽  
pp. 14001-14008
Author(s):  
Xiaoqiang Du ◽  
Guangyu Ma ◽  
Yanhong Wang ◽  
Xinghua Han ◽  
Xiaoshuang Zhang

The Ni3S2@NiOOH/NF catalyst with a core–shell structure exhibits a relatively low overpotential of 79 mV for HER at a current density of 10 mA cm−2, which is one of the best catalytic activities reported so far.


2018 ◽  
Vol 47 (45) ◽  
pp. 16305-16312 ◽  
Author(s):  
Xiaoqiang Du ◽  
Hui Su ◽  
Xiaoshuang Zhang

Using Co3O4@Co3S4-24 h as a bifunctional water splitting catalyst, an overpotential of ∼300 mV is obtained at a very low cell voltage of 1.53 V with a current density of 10 mA cm−2 in 1.0 M KOH.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Kang Jiang ◽  
Min Luo ◽  
Zhixiao Liu ◽  
Ming Peng ◽  
Dechao Chen ◽  
...  

AbstractMaximizing the catalytic activity of single-atom catalysts is vital for the application of single-atom catalysts in industrial water-alkali electrolyzers, yet the modulation of the catalytic properties of single-atom catalysts remains challenging. Here, we construct strain-tunable sulphur vacancies around single-atom Ru sites for accelerating the alkaline hydrogen evolution reaction of single-atom Ru sites based on a nanoporous MoS2-based Ru single-atom catalyst. By altering the strain of this system, the synergistic effect between sulphur vacancies and Ru sites is amplified, thus changing the catalytic behavior of active sites, namely, the increased reactant density in strained sulphur vacancies and the accelerated hydrogen evolution reaction process on Ru sites. The resulting catalyst delivers an overpotential of 30 mV at a current density of 10 mA cm−2, a Tafel slope of 31 mV dec−1, and a long catalytic lifetime. This work provides an effective strategy to improve the activities of single-atom modified transition metal dichalcogenides catalysts by precise strain engineering.


Sign in / Sign up

Export Citation Format

Share Document