Nanostructured cobalt-modified molybdenum carbides electrocatalysts for hydrogen evolution reaction

2016 ◽  
Vol 41 (48) ◽  
pp. 22899-22912 ◽  
Author(s):  
Saheed Bukola ◽  
Belabbes Merzougui ◽  
Stephen E. Creager ◽  
Mohammad Qamar ◽  
Larry R. Pederson ◽  
...  
2015 ◽  
Vol 51 (39) ◽  
pp. 8323-8325 ◽  
Author(s):  
Chunyong He ◽  
Juzhou Tao

Small size molybdenum carbides (2.5 nm for MoC and 5.0 nm for Mo2C) with clean surface on graphene were prepared for efficient and stable hydrogen evolution reaction catalysts.


Catalysts ◽  
2018 ◽  
Vol 8 (7) ◽  
pp. 294 ◽  
Author(s):  
Meng Chen ◽  
Yufei Ma ◽  
Yanqiang Zhou ◽  
Changqing Liu ◽  
Yanlin Qin ◽  
...  

The highly efficient electrochemical hydrogen evolution reaction (HER) provides a promising way to solve energy and environment problems. In this work, various transition metals (Fe, Co, Ni, Cu, Ag, and Pt) were selected to support on molybdenum carbides by a simple organic-inorganic precursor carburization process. X-ray diffraction (XRD) analysis results indicated that the β-Mo2C phase was formed in all metal-doped samples. X-ray photoelectron spectroscopy analysis indicated that the binding energy of Mo2+ species (Mo2C) shifted to a lower value after metal was doped on the molybdenum carbide surface. Comparing with pure β-Mo2C, the electrocatalytic activity for HER was improved by transition metal doping on the surface. Remarkably, the catalytic activity improvement was more obvious when Pt was doped on molybdenum carbide (2% Pt-Mo2C). The 2% Pt-Mo2C required a η10 of 79 mV, and outperformed that of pure β-Mo2C (η10 = 410 mV) and other transition metal doped molybdenum carbides, with a small Tafel slope (55 mV/dec) and a low onset overpotential (32 mV) in 0.5 M H2SO4. Also, the 2% Pt-Mo2C catalyst demonstrated a high stability for the HER in 0.5 M H2SO4. This work highlights a feasible strategy to explore efficient electrocatalysts with low cost via engineering on the composition and nanostructure.


Author(s):  
Yanlong Lv ◽  
Jian Ru Gong

The design of a universal synthesize strategy of long-term durable transition metal carbides catalysts with controllable nanostructure and sufficient active sites for hydrogen evolution reaction is challenging. Herein, the in-situ...


RSC Advances ◽  
2016 ◽  
Vol 6 (11) ◽  
pp. 9240-9246 ◽  
Author(s):  
Chunyong He ◽  
Juzhou Tao

Ultrasmall multiple phases molybdenum carbides nanocrystals (down to 2.5 nm) on graphene support were synthesized by a simplein situmethod. These hybrids show extraordinary high HER activity in acid media.


2020 ◽  
Vol 8 (38) ◽  
pp. 19879-19886
Author(s):  
Jiajia Huang ◽  
Jingyi Wang ◽  
Ruikuan Xie ◽  
Zhihong Tian ◽  
Guoliang Chai ◽  
...  

We designed a series of transition metal-modified molybdenum carbides in nitrogen doped carbon matrix for investigating and boosting the performance of Mo2C-based electrocatalysts in all-pH media by increasing the Mo2+ content in catalysts.


2017 ◽  
Vol 801 ◽  
pp. 7-13 ◽  
Author(s):  
Junpo Guo ◽  
Jie Wang ◽  
Cuijuan Xuan ◽  
Zexing Wu ◽  
Wen Lei ◽  
...  

2018 ◽  
Vol 284-286 ◽  
pp. 25-30 ◽  
Author(s):  
Jing Wan ◽  
Qipeng Liu ◽  
Tongtong Wang ◽  
Haomu Yuan ◽  
Pan Zhang ◽  
...  

2020 ◽  
Vol 8 (44) ◽  
pp. 23323-23329
Author(s):  
Jing Hu ◽  
Siwei Li ◽  
Yuzhi Li ◽  
Jing Wang ◽  
Yunchen Du ◽  
...  

Crystalline–amorphous Ni–Ni(OH)2 core–shell assembled nanosheets exhibit outstanding electrocatalytic activity and stability for hydrogen evolution under alkaline conditions.


2020 ◽  
Author(s):  
Elisabeth Hofmeister ◽  
Jisoo Woo ◽  
Tobias Ullrich ◽  
Lydia Petermann ◽  
Kevin Hanus ◽  
...  

Cobaloximes and their BF<sub>2</sub>-bridged analogues have emerged as promising non-noble metal catalysts for the photocatalytic hydrogen evolution reaction (HER). Herein we report the serendipitous discovery that double complex salts such as [Co(dmgh)<sub>2</sub>py<sub>2</sub>]<sup>+</sup>[Co(dmgBPh<sub>2</sub>)<sub>2</sub>Cl<sub>2</sub>]<sup>-</sup> can be obtained in good yields by treatment of commercially available [Co(dmgh)<sub>2</sub>pyCl] with triarylboranes. A systematic study on the use of such double complex salts and their single salts with simple counterions as photocatalysts revealed HER activities comparable or superior to existing cobaloxime catalysts and suggests ample opportunities for this compound class in catalyst/photosensitizer dyads and immobilized architectures. Preliminary electrochemical and spectroscopic studies indicate that one key advantage of these charged cobalt complexes is that the reduction potentials as well as the electrostatic interaction with charged photosensitizers can be tuned.


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