Halogen-Doped Carbon Dots on Amorphous Cobalt Phosphide as Robust Electrocatalysts for Overall Water Splitting

IF 24.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Advanced Energy Materials Pub Date : 2022-01-24 DOI:10.1002/aenm.202102573
Haoqiang Song, Jingkun Yu, Zhiyong Tang, Bai Yang, Siyu Lu
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引用次数: 115

Abstract

Designing a stable and efficient dual-functional catalyst for the hydrogen evolution and oxygen evolution reactions (HER/OER) is of great significance to the development of hydrogen production by water splitting. This work reports on novel halogen (X = F, Cl, and Br)-doped carbon dots modifying amorphous cobalt phosphide (X-CDs/CoP), which can be tuned by the choice of X-CDs to have urchin, Pinus bungeana, and Albizia julibrissin type structures. The different characteristics of the various X-CDs led to different formation mechanisms and final structures. As a bifunctional catalyst, urchin-shaped F-CDs/CoP crystals achieve superior electrocatalytic performance, exhibiting excellent HER/OER activity and sustained stability in an alkaline solution. For overall water splitting, they provide current density of 10 mA cm−2 and require a low cell voltage of 1.48 V in 1 M KOH. In addition, the catalytic performance shows negligible degradation after 100 h, thus demonstrating excellent long-term cycling stability. Density functional theory calculations show that the improved electrocatalytic performance of F-CDs/CoP catalysts is due to the coupling interface between CoP and F-CDs, which optimizes the hydrogen/oxygen adsorption energy and accelerates the water splitting kinetics. This work provides guidance for the rational design of transition metal phosphide electrocatalysts with outstanding performance.

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卤素掺杂碳点在非晶磷化钴表面作为整体水分解的稳健电催化剂
设计一种稳定高效的析氢、析氧双功能催化剂(HER/OER)对水裂解制氢技术的发展具有重要意义。本文报道了一种新型的卤素(X = F, Cl和Br)掺杂碳点修饰非晶态磷化钴(X- cds /CoP),可以通过选择X- cds来调整其具有海胆,白松木和合欢型结构。各种X-CDs的不同特性导致了不同的形成机制和最终结构。作为双功能催化剂,海胆形状的F-CDs/CoP晶体具有优异的电催化性能,在碱性溶液中表现出优异的HER/OER活性和持续的稳定性。对于整体水分解,它们提供10 mA cm−2的电流密度,并且在1 M KOH中需要1.48 V的低电池电压。此外,在100 h后,催化性能的退化可以忽略不计,因此具有良好的长期循环稳定性。密度泛函理论计算表明,F-CDs/CoP催化剂电催化性能的提高是由于CoP与F-CDs之间的耦合界面优化了氢/氧吸附能,加速了水裂解动力学。为合理设计性能优异的过渡金属磷化物电催化剂提供了指导。
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来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
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