scholarly journals Atomic Pt-Clusters Decoration Triggers a High-Rate Performance on Ni@Pd Bimetallic Nanocatalyst for Hydrogen Evolution Reaction in Both Alkaline and Acidic Medium

2020 ◽  
Vol 10 (15) ◽  
pp. 5155 ◽  
Author(s):  
Dinesh Bhalothia ◽  
Sheng-Po Wang ◽  
Shuan Lin ◽  
Che Yan ◽  
Kuan-Wen Wang ◽  
...  

The development of inexpensive and highly robust nanocatalysts (NCs) to boost electrochemical hydrogen evolution reaction (HER) strengthens the implementation of several emerging sustainable-energy technologies. Herein, we proposed a novel nano-architecture consisting of a hierarchical structured Ni@Pd nanocatalyst with Pt-clusters decoration on the surface (denoted by Ni@Pd-Pt) for HER application in acidic (0.5 M H2SO4) and alkaline (0.1 M KOH) mediums. The Ni@Pd-Pt NC is fabricated on a carbon black support via a “self-aligned” heterogeneous nucleation-crystal growth mechanism with 2 wt.% Pt-content. As-prepared Ni@Pd-Pt NC outperforms the standard Pt/C (30 wt.% Pt) catalyst in HER and delivers high-rate catalytic performance with an ultra-low overpotential (11.5 mV) at the cathodic current density of 10 mA∙cm−2 in alkaline medium, which is 161.5 mV and 14.5 mV less compared to Ni@Pd (173 mV) and standard Pt/C (26 mV) catalysts, respectively. Moreover, Ni@Pd-Pt NC achieves an exactly similar Tafel slope (42 mV∙dec−1) to standard Pt/C, which is 114 mV∙dec−1 lesser when compared to Ni@Pd NC. Besides, Ni@Pd-Pt NC exhibits an overpotential value of 37 mV at the current density of 10 mA cm−2 in acidic medium, which is competitive to standard Pt/C catalyst. By utilizing physical characterizations and electrochemical analysis, we demonstrated that such an aggressive HER activity is dominated by the increased selectivity during HER due to the reduced competition between intermediate products on the non-homogeneous NC surface. This phenomenon can be rationalized by electron localization owing to the electronegative difference (χPt > χPd > χNi) and strong lattice mismatch at the Ni@Pd heterogeneous binary interfaces. We believe that the obtained results will significantly provide a facile design strategy to develop next-generation heterogenous NCs for HER and related green-energy applications

2019 ◽  
Vol 55 (65) ◽  
pp. 9665-9668 ◽  
Author(s):  
Quan Zhang ◽  
Fang Luo ◽  
Hao Hu ◽  
Ruizhi Xu ◽  
Konggang Qu ◽  
...  

W/W2C heterostructured nanoparticles encapsulated by N,P dual-doped carbon require low overpotentials of 55 mV and 82 mV vs. RHE to achieve cathodic current density of 10 mA cm−2 in acidic and alkaline electrolytes, respectively.


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.


2015 ◽  
Vol 3 (11) ◽  
pp. 5783-5788 ◽  
Author(s):  
Kai Zhang ◽  
Yang Zhao ◽  
Diyu Fu ◽  
Yujin Chen

Highly conductive N-doped carbon nanotubes embedded with molybdenum carbide nanocrystals with a size less than 3 nm exhibit superior activity for the hydrogen evolution reaction, including small overpotential, large cathodic current density and high exchange current density.


2019 ◽  
Vol 55 (15) ◽  
pp. 2186-2189 ◽  
Author(s):  
Alpesh K. Sharma ◽  
Hemant Joshi ◽  
Kasinath Ojha ◽  
Ajai K. Singh

The cathodic current density (cd) of GO-Co2P is 20/100 mA cm−2 at an overpotential of 80/154 mV. At 100 mA cm−2 cd, stability is observed for 70 h.


2018 ◽  
Vol 47 (39) ◽  
pp. 13792-13799 ◽  
Author(s):  
Jiban K. Das ◽  
Aneeya K. Samantara ◽  
Arpan K. Nayak ◽  
Debabrata Pradhan ◽  
J. N. Behera

A single step scalable synthesis for vanadium disulphide (VS2) was developed and the resulting material shows a better electrocatalytic performance in terms of a low onset potential (15 mV), a lower Tafel slope (36 mV dec−1) and needs only 41 mV to deliver a state-of-the-art current density of 10 mA cm−2.


2017 ◽  
Vol 5 (24) ◽  
pp. 12043-12047 ◽  
Author(s):  
Yaxiao Guo ◽  
Zhaoyang Yao ◽  
Changshuai Shang ◽  
Erkang Wang

Owing to the prominent synergistic effects, P-Co2Mo3Se/CFC hybrid catalyst exhibits a superior HER activity with a small overpotential of 71 mV at cathodic current density of 10 mA cm−2, and a small Tafel slope of 43.6 mV dec−1, as well as excellent cycling stability.


Crystals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1040 ◽  
Author(s):  
Getachew Solomon ◽  
Raffaello Mazzaro ◽  
Vittorio Morandi ◽  
Isabella Concina ◽  
Alberto Vomiero

Molybdenum sulfide (MoS2) has emerged as a promising catalyst for hydrogen evolution applications. The synthesis method mainly employed is a conventional hydrothermal method. This method requires a longer time compared to other methods such as microwave synthesis methods. There is a lack of comparison of the two synthesis methods in terms of crystal morphology and its electrochemical activities. In this work, MoS2 nanosheets are synthesized using both hydrothermal (HT-MoS2) and advanced microwave methods (MW-MoS2), their crystal morphology, and catalytical efficiency towards hydrogen evolution reaction (HER) were compared. MoS2 nanosheet is obtained using microwave-assisted synthesis in a very short time (30 min) compared to the 24 h hydrothermal synthesis method. Both methods produce thin and aggregated nanosheets. However, the nanosheets synthesized by the microwave method have a less crumpled structure and smoother edges compared to the hydrothermal method. The as-prepared nanosheets are tested and used as a catalyst for hydrogen evolution results in nearly similar electrocatalytic performance. Experimental results showed that: HT-MoS2 displays a current density of 10 mA/cm2 at overpotential (−280 mV) compared to MW-MoS2 which requires −320 mV to produce a similar current density, suggesting that the HT-MoS2 more active towards hydrogen evolutions reaction.


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