Amorphous nanomaterials have emerged as potential candidates for energy storage and conversion owing to their amazing physicochemical properties.Recent studies have proved that the manipulation of amorphous nanomater...Amorphous nanomaterials have emerged as potential candidates for energy storage and conversion owing to their amazing physicochemical properties.Recent studies have proved that the manipulation of amorphous nanomaterials can further enhance electrochemical performance.To date,various feasible strategies have been proposed,of which amorphous/crystalline(a-c)heterointerface engineering is deemed an effective approach to break through the inherent activity limitations of electrode materials.The following review discusses recent research progress on a-c heterointerfaces for enhanced electrochemical processes.The general strategies for synthesizing ac heterojunctions are first summarized.Subsequently,we highlight various advanced applications of a-c heterointerfaces in the field of electrochemistry,including for supercapacitors,batteries,and electrocatalysts.We also elucidate the synergistic mechanism of the crystalline phase and amorphous phase for electrochemical processes.Lastly,we summarize the challenges,present our personal opinions,and offer a critical perspective on the further development of a-c nanomaterials.展开更多
The current bottleneck facing further developments in fuel cells is the lack of durable electrocatalysts with satisfactory activity. In this study, a simple and fast one-pot wet-chemical method is proposed to synthesi...The current bottleneck facing further developments in fuel cells is the lack of durable electrocatalysts with satisfactory activity. In this study, a simple and fast one-pot wet-chemical method is proposed to synthesize novel Au@Pt star-like bimetallic nanocrystals （Au@Pt SLNCs） with a low Pt/Au ratio of 1：4, which show great electrocatalytic properties and outstanding stability toward the electro-oxidation reactions commonly found in fuel cells. The star-like Au core （90±20 nm） is partially coated with 5 nm Pt nanocluster shells, a morphology which creates a large amount of boundaries and edges, thus tuning the surface electronic structure as demonstrated by X-ray photoelectron spectroscopy and CO-stripping measurements. This promotes excellent electrocatalytic performance towards the formic acid oxidation reaction in acidic media and the ethanol oxidation reaction in alkaline media, compared to commercial Pt or Au@Pt triangular nanoprisms, in which the Au core is fully coated by a Pt shell. Au@Pt SLNCs have the highest current density within the dehydrogenation potential range, needing the least potential to achieve a certain current density as well as the highest long-term stability. Because of the small amount of Pt usage, very fast synthesis, excellent electrocatalytic activity and durability, the proposed Au@Pt SLNCs have a promising practical application in fuel cells.展开更多
The advancement of next-generation energy technologies calls for rationally designed and fabricated electrode materials that have desirable structures and satisfactory performance.Three-dimensional(3D)self-supported a...The advancement of next-generation energy technologies calls for rationally designed and fabricated electrode materials that have desirable structures and satisfactory performance.Three-dimensional(3D)self-supported amorphous nanomaterials have attracted great enthusiasm as the cornerstone for building high-performance nanodevices.In particular,tremendous efforts have been devoted to the design,fabrication,and evaluation of self-supported amorphous nanomaterials as electrodes for energy storage and conversion devices in the past decade.However,the electrochemical performance of devices assembled with 3D self-supported amorphous nanomaterials still remains to be dramatically promoted to satisfy the demands for more practical applications.In this review,we aim to outline the achievements made in recent years in the development of 3D self-supported amorphous nanomaterials for a broad range of energy storage and conversion processes.We firstly summarize different synthetic strategies employed to synthesize 3D nanomaterials and to tailor their composition,morphology,and structure.Then,the performance of these 3D self-supported amorphous nanomaterials in their corresponding energy-related reactions is highlighted.Finally,we draw out our comprehensive understanding towards both challenges and prospects of this promising field,where valuable guidance and inspiration will surely facilitate further development of 3D self-supported amorphous nanomaterials,thus enabling more highly efficient energy storage and conversion devices that play a key role in embracing a sustainable energy future.展开更多
基金This work is supported by the National Natural Science Foundation of China(52272181,51532001,U1910208,51872016)China Postdoctoral Science Foundation(2020TQ0023 and 2020M680295).
文摘Amorphous nanomaterials have emerged as potential candidates for energy storage and conversion owing to their amazing physicochemical properties.Recent studies have proved that the manipulation of amorphous nanomaterials can further enhance electrochemical performance.To date,various feasible strategies have been proposed,of which amorphous/crystalline(a-c)heterointerface engineering is deemed an effective approach to break through the inherent activity limitations of electrode materials.The following review discusses recent research progress on a-c heterointerfaces for enhanced electrochemical processes.The general strategies for synthesizing ac heterojunctions are first summarized.Subsequently,we highlight various advanced applications of a-c heterointerfaces in the field of electrochemistry,including for supercapacitors,batteries,and electrocatalysts.We also elucidate the synergistic mechanism of the crystalline phase and amorphous phase for electrochemical processes.Lastly,we summarize the challenges,present our personal opinions,and offer a critical perspective on the further development of a-c nanomaterials.
文摘The current bottleneck facing further developments in fuel cells is the lack of durable electrocatalysts with satisfactory activity. In this study, a simple and fast one-pot wet-chemical method is proposed to synthesize novel Au@Pt star-like bimetallic nanocrystals （Au@Pt SLNCs） with a low Pt/Au ratio of 1：4, which show great electrocatalytic properties and outstanding stability toward the electro-oxidation reactions commonly found in fuel cells. The star-like Au core （90±20 nm） is partially coated with 5 nm Pt nanocluster shells, a morphology which creates a large amount of boundaries and edges, thus tuning the surface electronic structure as demonstrated by X-ray photoelectron spectroscopy and CO-stripping measurements. This promotes excellent electrocatalytic performance towards the formic acid oxidation reaction in acidic media and the ethanol oxidation reaction in alkaline media, compared to commercial Pt or Au@Pt triangular nanoprisms, in which the Au core is fully coated by a Pt shell. Au@Pt SLNCs have the highest current density within the dehydrogenation potential range, needing the least potential to achieve a certain current density as well as the highest long-term stability. Because of the small amount of Pt usage, very fast synthesis, excellent electrocatalytic activity and durability, the proposed Au@Pt SLNCs have a promising practical application in fuel cells.
基金This work was supported by the National Natural Science Foundation of China(Nos.52272181,51872016,and 52201261)China Postdoctoral Science Foundation(Nos.2020TQ0023 and 2020M680295).
文摘The advancement of next-generation energy technologies calls for rationally designed and fabricated electrode materials that have desirable structures and satisfactory performance.Three-dimensional(3D)self-supported amorphous nanomaterials have attracted great enthusiasm as the cornerstone for building high-performance nanodevices.In particular,tremendous efforts have been devoted to the design,fabrication,and evaluation of self-supported amorphous nanomaterials as electrodes for energy storage and conversion devices in the past decade.However,the electrochemical performance of devices assembled with 3D self-supported amorphous nanomaterials still remains to be dramatically promoted to satisfy the demands for more practical applications.In this review,we aim to outline the achievements made in recent years in the development of 3D self-supported amorphous nanomaterials for a broad range of energy storage and conversion processes.We firstly summarize different synthetic strategies employed to synthesize 3D nanomaterials and to tailor their composition,morphology,and structure.Then,the performance of these 3D self-supported amorphous nanomaterials in their corresponding energy-related reactions is highlighted.Finally,we draw out our comprehensive understanding towards both challenges and prospects of this promising field,where valuable guidance and inspiration will surely facilitate further development of 3D self-supported amorphous nanomaterials,thus enabling more highly efficient energy storage and conversion devices that play a key role in embracing a sustainable energy future.
