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一种用于高效析氢的负载于氮、磷共掺杂石墨烯上的磷化钴的绿色合成策略。

A Green Synthesis Strategy for Cobalt Phosphide Deposited on N, P Co-Doped Graphene for Efficient Hydrogen Evolution.

作者信息

Ma Jingwen, Wang Jun, Li Junbin, Tian Ying, Zhang Tianai

机构信息

School of Chemical and Environmental Engineering, China University of Mining and Technology (Beijing), Beijing 100083, China.

PetroChina Planning and Engineering Institute, Beijing 100083, China.

出版信息

Materials (Basel). 2023 Sep 7;16(18):6119. doi: 10.3390/ma16186119.

DOI:10.3390/ma16186119
PMID:37763395
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10532637/
Abstract

The exploitation of electrocatalysts with high activity and durability for the hydrogen evolution reaction is significant but also challenging for future energy systems. Transition metal phosphides (TMPs) have attracted a lot of attention due to their effective activity for the hydrogen evolution reaction, but the complicated preparation of metal phosphides remains a bottleneck. In this study, a green fabrication method is designed and proposed to construct N, P co-doped graphene (NPG)-supported cobalt phosphide (CoP) nanoparticles by using DNA as both N and P sources. Thanks to the synergistic effect of NPG and CoP, the CoP/NPG shows effective activity with a small overpotential of 144 mV and a low Tafel slope of 72 mV dec for the hydrogen evolution reaction. This study describes a successful green synthesis strategy for the preparation of high-performance TMPs.

摘要

开发具有高活性和耐久性的用于析氢反应的电催化剂对于未来能源系统而言意义重大,但也具有挑战性。过渡金属磷化物(TMPs)因其对析氢反应具有有效的活性而备受关注,但其复杂的制备过程仍然是一个瓶颈。在本研究中,设计并提出了一种绿色制造方法,通过使用DNA作为氮和磷源来构建氮、磷共掺杂石墨烯(NPG)负载的磷化钴(CoP)纳米颗粒。由于NPG和CoP的协同效应,CoP/NPG对析氢反应表现出有效的活性,过电位低至144 mV,塔菲尔斜率为72 mV dec-1。本研究描述了一种成功制备高性能TMPs的绿色合成策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/d0a8f1a720eb/materials-16-06119-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/ea7fdc853e59/materials-16-06119-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/29b5b4302d3a/materials-16-06119-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/143859dbe86f/materials-16-06119-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/05b847fc8c81/materials-16-06119-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/d0a8f1a720eb/materials-16-06119-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/ea7fdc853e59/materials-16-06119-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/29b5b4302d3a/materials-16-06119-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/143859dbe86f/materials-16-06119-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/05b847fc8c81/materials-16-06119-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd4/10532637/d0a8f1a720eb/materials-16-06119-g005.jpg

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本文引用的文献

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Nanomaterials (Basel). 2023 May 18;13(10):1667. doi: 10.3390/nano13101667.
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From atomic bonding to heterointerfaces: CoP/WC constructed by lacunary polyoxometalates induced strategy as efficient hydrogen evolution electrocatalysts at all pH values.从原子键合到异质界面:通过乏氧多金属氧酸盐诱导策略构建的 CoP/WC 作为在所有 pH 值下都高效的析氢电催化剂。
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Tiny NiS boosting MoS hydrogen evolution in alkali by enlarging coupling boundaries and stimulating basal plane.
微小的 NiS 通过扩大耦合边界和激发基面来促进 MoS 在碱中的析氢。
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MoS/NiSe/rGO Multiple-Interfaced Sandwich-like Nanostructures as Efficient Electrocatalysts for Overall Water Splitting.MoS/NiSe/rGO多界面三明治状纳米结构作为高效的全水解电催化剂
Nanomaterials (Basel). 2023 Feb 16;13(4):752. doi: 10.3390/nano13040752.
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CoP/CoP Encapsulated in Carbon Nanotube Arrays to Construct Self-Supported Electrodes for Overall Electrochemical Water Splitting.将 CoP/CoP 封装在碳纳米管阵列中,构建用于全电化学水分解的自支撑电极。
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