Excavated cubic platinum–iridium alloy nanocrystals with high-index facets as highly efficient electrocatalysts in N2 fixation to NH3

2019 ◽  
Vol 55 (63) ◽  
pp. 9335-9338 ◽  
Author(s):  
Yu-Jie Mao ◽  
Lu Wei ◽  
Xin-Sheng Zhao ◽  
Yong-Sheng Wei ◽  
Jian-Wei Li ◽  
...  

Excavated cubic Pt93Ir7 alloy nanocrystals enclosed by high-index {710} facets exhibit excellent electrocatalytic properties for the nitrogen reduction reaction (NRR) with high faradaic efficiency (40.8%) and NH3 yield (28 μg h−1 cm−2).

RSC Advances ◽  
2020 ◽  
Vol 10 (49) ◽  
pp. 29575-29579
Author(s):  
Meng Wang ◽  
Feifei Li ◽  
Juan Liu

Fe2O3 nanoparticles generated from a glycerine-based synthesis can be applied as highly efficient catalysts for the electrochemical nitrogen reduction reaction.


2018 ◽  
Vol 54 (42) ◽  
pp. 5323-5325 ◽  
Author(s):  
Xiaoping Zhang ◽  
Rong-Mei Kong ◽  
Huitong Du ◽  
Lian Xia ◽  
Fengli Qu

A VN nanowire array on carbon cloth (VN/CC) as a high-performance catalyst for the nitrogen reduction reaction (NRR) affords high ammonia yield (2.48 × 10−10 mol−1 s−1 cm−2) and faradaic efficiency (3.58%) at −0.3 V versus RHE in 0.1 M HCl.


Author(s):  
Qiuling Jiang ◽  
Yanan Meng ◽  
Kai Li ◽  
Ying Wang ◽  
Zhijian Wu

Abstract Searching for highly efficient electrocatalysts toward nitrogen reduction reaction (NRR) is an important but challenging task for nitrogen utilization in industry. Here we have systematically designed a series of hetero-diatomic catalysts (DACs), in which transition metal atoms (Ti, V, Cr, Mn, Fe, Co, and Ni) are dispersed on PC6 monolayer to form AB@PC6 (A, B= Ti, V, Cr, Mn, Fe, Co, and Ni). Employing density functional theory (DFT) calculation, the V and Cr co-doped PC6 monolayer (VCr@PC6) among the 21 AB@PC6 catalysts is the most promising catalyst due to its low limiting potential of -0.41V, relatively low energy barrier, and high ammonia selectivity toward hydrogen evolution reaction (HER). Insights on the high NRR activity of VCr@PC6 are also explored. The synergistic effect in DACs facilitates the electron transfer from metal pairs to PC6 monolayer, as well as suppresses the HER, leading to high selectivity and Faradaic efficiency. This work not only aims to seek the efficient DACs towards N2 reduction but also provides insights towards synergistic effects between hetero-atoms for the rational design of DACs.


2021 ◽  
pp. 150801
Author(s):  
Jiabin Tan ◽  
Xiaobo H ◽  
Fengxiang Yin ◽  
Xin Liang ◽  
Guoru Li ◽  
...  

Small ◽  
2015 ◽  
Vol 12 (4) ◽  
pp. 524-533 ◽  
Author(s):  
Yuchen Qin ◽  
Xin Zhang ◽  
Xiaoping Dai ◽  
Hui Sun ◽  
Ying Yang ◽  
...  

2021 ◽  
Author(s):  
Shengbo Zhang ◽  
Miaomiao Han ◽  
Tongfei Shi ◽  
Haimin Zhang ◽  
Yue Lin ◽  
...  

Abstract The intriguing features of single-atom catalysts (SACs) could bring catalysis into a new paradigm, however, controllably synthesising SACs with desired SA loadings and coordination forms are challenging. Here, we report an adsorption-regulated approach to precisely control the synthesis of bimetallic Fe-Co SAs on carbon. Bacterial cellulose (BC) is utilised as an adsorption regulator to controllably impregnate Fe3+/Co2+ on BC and through carbonisation to anchor Fe-Co SAs on BC-derived carbon via bimetallic [(O-C2)3Fe-Co(O-C2)3] coordination with desired Fe/Co contents and atomic ratios. Under electrocatalytic nitrogen reduction reaction (NRR) conditions, [(O-C2)3Fe-Co(O-C2)3] is operando transformed to [(O-C2)3Fe-Co(O-C)C2] that promotes and sustains NRR performance. A superb ammonia yield of 574.8 ± 35.3 μg h-1 mgcat.-1 with an exceptional faradaic efficiency of 73.2 ± 4.6% are obtained from an electrocatalyst with the highest bimetallic Fe-Co site density. The exemplified synthetic approach would be of generically applicable to controllably anchor SAs on carbon that enables meaningfully investigate and rationally design SACs.


2020 ◽  
Vol 56 (3) ◽  
pp. 446-449 ◽  
Author(s):  
Shenglin Xiao ◽  
Fang Luo ◽  
Hao Hu ◽  
Zehui Yang

Boron and nitrogen dual-doped carbon nanospheres show exceptional nitrogen reduction reaction activity, with an NH3 yield rate of 15.7 μgNH3 h−1 mgcat.−1 and Faradaic efficiency of 8.1% at −0.4 V vs. RHE in acidic electrolyte.


Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1777 ◽  
Author(s):  
Ruijie Guo ◽  
Min Hu ◽  
Weiqing Zhang ◽  
Jia He

Exploration of efficient catalysts is a priority for the electrochemical nitrogen reduction reaction (NRR) in order to receive a high product yield rate and faradaic efficiency of NH3, under ambient conditions. In the present contribution, the binding free energy of N2, NNH, and NH2 were used as descriptors to screen the potential NRR electrocatalyst among different single or binuclear transition metal atoms on N-doped nanoporous graphene. Results showed that the binuclear Mo catalyst might exhibit the highest catalytic activity. Further free energy profiles confirmed that binuclear Mo catalysts possess the lowest potential determining step (hydrogenation of NH2* to NH3). The improved activities could be ascribed to a down-shift of the density of states for Mo atoms. This investigation could contribute to the design of a highly active NRR electrocatalyst.


Sign in / Sign up

Export Citation Format

Share Document