scholarly journals Influence of nickel doping on MnO2 nanoflowers as electrocatalyst for oxygen reduction reaction

2021 ◽  
Vol 3 (9) ◽  
Author(s):  
Ababay Ketema Worku ◽  
Delele Worku Ayele ◽  
Nigus Gabbiye Habtu

Abstract Doping is promising strategy for the alteration of nanomaterials to enhance their optical, electrical, and catalytic activities. The development of electrocatalysts for oxygen reduction reactions (ORR) with excellent activity, low cost and durability is essential for the large-scale utilization of energy storage devices such as batteries. In this study, MnO2 and Ni-doped MnO2 nanowires were prepared through a simple co-perception technique. The influence of nickel concentration on electrochemical performance was studied using linear sweep voltammetry and cyclic voltammetry. The morphological, thermal, structural, and optical properties  of MnO2 and Ni-doped MnO2 nanowires were examined by SEM, ICP-OES, FT-IR, XRD, UV–Vis, BET and TGA/DTA. Morphological analyses showed that pure MnO2 and Ni-doped MnO2 had flower-like and nanowire structures, respectively. The XRD study confirmed the phase transformation from ε to α and β phases of MnO2 due to the dopant. It was also noted from the XRD studies that the crystallite sizes of pure MnO2 and Ni-doped MnO2 were in the range of 2.25–6.6 nm. The band gaps of MnO2 and 0.125 M Ni-doped MnO2 nanoparticles were estimated to be 2.78 and 1.74 eV, correspondingly, which can be seen from UV–Vis. FTIR spectroscopy was used to determine the presence of functional groups and M–O bonds (M = Mn, Ni). The TGA/TDA examination showed that Ni-doping in MnO2 led to an improvement in its thermal properties. The cyclic voltammetry  results exhibited that Ni-doped MnO2 nanowires have remarkable catalytic performance for ORR in 0.1 M KOH alkaline conditions. This work contributes to the facile preparation of highly active and durable catalysts with improved catalytic performance mainly due to the predominance of nickel. Article Highlights MnO2 and Ni-doped MnO2 nanowires were synthesized via a facile co-perception approach. Nickel doping in MnO2 induces the formation of wire-like nanostructures. Nickel doping enhances the electrochemical activity and thermal stability of MnO2 nanoflowers. The addition of nickel into MnO2 promoted the catalytic activity for oxygen reduction reaction. A higher catalytic activity was achieved in 0.125 M Ni-MnO2 nanowires. Graphic abstract

NANO ◽  
2020 ◽  
Vol 15 (09) ◽  
pp. 2050115
Author(s):  
Zixu Wu ◽  
Guangxing Li ◽  
Qin Liao ◽  
Ruida Ding ◽  
Xuze Zuo ◽  
...  

Enhancing the catalytic activity of manganese oxide in oxygen reduction reaction (ORR) is a key issue for its large-scale application in metal-air fuel cells. Ag-doped [Formula: see text]-MnO2 nanowires without Ag or Ag2O have been successfully synthesized via a facile hydrothermal method, and the changes in both the structure and electrochemical catalytic performances after Ag doping are investigated. Compared with the pristine [Formula: see text]-MnO2, the as-prepared Ag-doped MnO2 exhibits a significantly enhanced catalytic activity in both ORR and Mg-air fuel cell application. With Ag/Mn ratio of 1:25, Ag-doped MnO2 exhibits a typical 4e-reaction pathway and presents a 163 mV higher half-wave potential than that of the pristine [Formula: see text]-MnO2. Furthermore, it demonstrates a power density of 75.1[Formula: see text]mW[Formula: see text]cm[Formula: see text] at current density of 134.5[Formula: see text]mA[Formula: see text]cm[Formula: see text] in the Mg-air fuel cells. The enhanced ORR performances are considered to be contributed from the activation of surface lattice oxygen, the improvement in conductivity and the increase in oxygen vacancies of [Formula: see text]-MnO2. These findings provide new understanding for developing high-performance manganese oxide catalysts.


2015 ◽  
Vol 3 (11) ◽  
pp. 5850-5858 ◽  
Author(s):  
Haibo Li ◽  
Cancan Ren ◽  
Shuling Xu ◽  
Lei Wang ◽  
Qiaoli Yue ◽  
...  

Alloying Pt with both Te and Cu could effectively improve ternary TeCuPt catalytic activity for electronic and geometric structure effects.


RSC Advances ◽  
2016 ◽  
Vol 6 (55) ◽  
pp. 50349-50357 ◽  
Author(s):  
Guiting Xie ◽  
Bohong Chen ◽  
Zhongqing Jiang ◽  
Xiaojun Niu ◽  
Si Cheng ◽  
...  

A simple method has been adopted for the synthesis of Co3O4 nanoparticles encapsulated in graphene supported carbon matrix, which could exhibit higher catalytic performance for oxygen reduction reaction than the commercial Pt/C.


Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 623
Author(s):  
Mengfan Shen ◽  
Ziwei Meng ◽  
Tong Xue ◽  
Hongfang Shen ◽  
Xiang-Hui Yan

To explore high-performing alternatives to platinum-based catalysts is highly desirable for lowering costs and thus promoting fuel cell commercialization. Herein, self-supported Fe-N-C materials were prepared by the pyrolysis of dual precursors including EDTA ferric sodium (EDTAFeNa) and melamine (MA), followed by acid-leaching and final annealing. Towards an oxygen reduction reaction (ORR) in 0.1 M KOH, the as-prepared MA/EDTAFeNa-HT2 delivered onset (Eonset) and half-wave (E1/2) potentials of 0.97 and 0.84 V vs. RHE, respectively, identical with that of a state-of-the-art Pt/C catalyst, accompanied with predominantly a four-electron pathway. The introduction of MA and extension of acid-leaching promoted a positive shift of 50 mV for E1/2 relative to that of only the EDTAFeNa-derived counterpart. It was revealed that the enhancement of ORR activity is attributed to a decrease in magnetic Fe species and increase in pyridinic/quanternary nitrogen content whilst nearly excluding effects of the graphitization degree, variety of crystalline iron species, and mesoscopic structure. The usage of dual precursors exhibited great potential for the large-scale production of inexpensive and efficient Fe-N-C materials.


2017 ◽  
Vol 5 (42) ◽  
pp. 22163-22169 ◽  
Author(s):  
Baolong Zhou ◽  
Liangzhen Liu ◽  
Pingwei Cai ◽  
Guang Zeng ◽  
Xiaoqiang Li ◽  
...  

Two nitrogen-rich porous organic polymers (POPs) were prepared via Schiff base chemistry. Carbonization of these POPs results in porous carbon nanohybrids which exhibit excellent catalytic activity toward the oxygen reduction reaction (ORR).


2016 ◽  
Vol 120 (40) ◽  
pp. 22895-22902 ◽  
Author(s):  
Xuecheng Cao ◽  
Tao Hong ◽  
Ruizhi Yang ◽  
Jing-Hua Tian ◽  
Changrong Xia ◽  
...  

2022 ◽  
Author(s):  
Huixin Ma ◽  
Daijie Deng ◽  
Honghui Zhang ◽  
Feng Chen ◽  
Junchao Qian ◽  
...  

Nitrogen-coordinated single-atom manganese in multi-dimensional nitrogen-doped carbon electrocatalysts (Mn-NC) was successful constructed by combing two-dimensional nanosheets and one-dimensional nanofibers. The Mn-NC exhibited excellent oxygen reduction reaction catalytic activity with half-wave...


Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 955 ◽  
Author(s):  
Jing Liu ◽  
Jiao Yin ◽  
Bo Feng ◽  
Tao Xu ◽  
Fu Wang

The Pt particles within diameters of 1–3 nm known as Pt nanoclusters (NCs) are widely considered to be satisfactory oxygen reduction reaction (ORR) catalysts due to higher electrocatalytic performance and cost effectiveness. However, the utilization of such smaller Pt NCs is always limited by the synthesis strategies, stability and methanol tolerance of Pt. Herein, unprotected Pt NCs (~2.2 nm) dispersed on carbon nanotubes (CNTs) were prepared via a modified top-down approach using liquid Li as a solvent to break down the bulk Pt. Compared with the commercial Pt/C, the resultant Pt NCs/CNTs catalyst (Pt loading: 10 wt.%) exhibited more desirable ORR catalytic performance in 0.1 M HClO4. The specific activity (SA) and mass activity (MA) at 0.9 V for ORR over Pt NCs/CNTs were 2.5 and 3.2 times higher than those over the commercial Pt/C (Pt loading: 20 wt.%). Meanwhile, the Pt NCs/CNTs catalyst demonstrated more satisfactory stability and methanol tolerance. Compared with the obvious loss (~69%) of commercial Pt/C, only a slight current decrease (~10%) was observed for Pt NCs/CNTs after the chronoamperometric measurement for 2 × 104 s. Hence, the as-prepared Pt NCs/CNTs material displays great potential as a practical ORR catalyst.


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