Noble-Metal-Free Multicomponent Nanointegration for Sustainable Energy Conversion

2021 ◽  
Author(s):  
Haijiao Lu ◽  
Julie Tournet ◽  
Kamran Dastafkan ◽  
Yun Liu ◽  
Yun Hau Ng ◽  
...  
2020 ◽  
Vol 49 (14) ◽  
pp. 4230-4243
Author(s):  
James D. Shipp ◽  
Heather Carson ◽  
Steven J. P. Spall ◽  
Simon C. Parker ◽  
Dimitri Chekulaev ◽  
...  

M(NN)(CO)3X (M = Re, Mn) complexes with a bulky diimine ligand catalyse electrochemical reduction of CO2 with high TON. A noble-metal free system of the Mn-complex photosensitised by a Zn-porphyrin photocatalytically reduces CO2 under visible light.


ACS Catalysis ◽  
2016 ◽  
Vol 6 (9) ◽  
pp. 6198-6206 ◽  
Author(s):  
Weiguang Ma ◽  
Jingfeng Han ◽  
Wei Yu ◽  
Dong Yang ◽  
Hong Wang ◽  
...  

Author(s):  
Rongming Cai ◽  
Min Ju ◽  
Jinxi Chen ◽  
Jiazheng Ren ◽  
Jun Yu ◽  
...  

Recent advances in characterization techniques and surface modification strategies of energy conversion catalysts are reviewed, with an emphasis on surface defect engineering, surface crystalline property modulation, surface structure tailoring and heterointerface construction.


2021 ◽  
Author(s):  
Chang-Xin Zhao ◽  
Jia-Ning Liu ◽  
Juan Wang ◽  
Ding Ren ◽  
Bo-Quan Li ◽  
...  

Bifunctional oxygen reduction and evolution constitute the core processes for sustainable energy storage. The advances on noble-metal-free bifunctional oxygen electrocatalysts are reviewed.


2019 ◽  
Vol 3 (5) ◽  
pp. 573-578 ◽  
Author(s):  
Kwanwoo Shin

Living cells naturally maintain a variety of metabolic reactions via energy conversion mechanisms that are coupled to proton transfer across cell membranes, thereby producing energy-rich compounds. Until now, researchers have been unable to maintain continuous biochemical reactions in artificially engineered cells, mainly due to the lack of mechanisms that generate energy-rich resources, such as adenosine triphosphate (ATP) and reduced nicotinamide adenine dinucleotide (NADH). If these metabolic activities in artificial cells are to be sustained, reliable energy transduction strategies must be realized. In this perspective, this article discusses the development of an artificially engineered cell containing a sustainable energy conversion process.


Langmuir ◽  
2021 ◽  
Vol 37 (11) ◽  
pp. 3321-3330
Author(s):  
Rong Liang ◽  
Yanwen Wang ◽  
Chao Qin ◽  
Xuehua Chen ◽  
Zhizhen Ye ◽  
...  

Author(s):  
Erick Leonar Ribeiro ◽  
Elijah M Davis ◽  
Mahshid Mokhtarnejad ◽  
Sheng Hu ◽  
Dibyendu Mukherjee ◽  
...  

Rapidly expanding global energy demands due to fast-paced human-technology interfaces have propelled fuel cell technology as a sustainable energy-conversion alternative. Nonetheless, the rational development of such technology demands the engineering...


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yongmeng Wu ◽  
Cuibo Liu ◽  
Changhong Wang ◽  
Yifu Yu ◽  
Yanmei Shi ◽  
...  

AbstractElectrocatalytic alkyne semi-hydrogenation to alkenes with water as the hydrogen source using a low-cost noble-metal-free catalyst is highly desirable but challenging because of their over-hydrogenation to undesired alkanes. Here, we propose that an ideal catalyst should have the appropriate binding energy with active atomic hydrogen (H*) from water electrolysis and a weaker adsorption with an alkene, thus promoting alkyne semi-hydrogenation and avoiding over-hydrogenation. So, surface sulfur-doped and -adsorbed low-coordinated copper nanowire sponges are designedly synthesized via in situ electroreduction of copper sulfide and enable electrocatalytic alkyne semi-hydrogenation with over 99% selectivity using water as the hydrogen source, outperforming a copper counterpart without surface sulfur. Sulfur anion-hydrated cation (S2−-K+(H2O)n) networks between the surface adsorbed S2− and K+ in the KOH electrolyte boost the production of active H* from water electrolysis. And the trace doping of sulfur weakens the alkene adsorption, avoiding over-hydrogenation. Our catalyst also shows wide substrate scopes, up to 99% alkenes selectivity, good reducible groups compatibility, and easily synthesized deuterated alkenes, highlighting the promising potential of this method.


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