调控单位点M-N-C电催化剂的电子结构提升二氧化碳还原性能

doi:10.3866/PKU.WHXB202208033

Abstract

Abstract:

The current global population and economy depends on fossil fuel consumption; however, the uncontrolled exploitation of fossil fuels has caused a series of energy crises and environmental problems, such as energy exhaustion, annual temperature rise, climate deterioration, and ocean acidification, which have already threatened the sustainable development of all living organisms. Therefore, finding renewable and reliable energy sources as well as reducing carbon dioxide (CO₂) emissions have become the key focus in recent years. During the electrocatalytic CO₂ reduction reaction (CO₂RR) under relatively mild conditions, CO₂ is converted into valuable products, such as C1, C2, and C2+ hydrocarbons, which is an effective strategy towards realizing "carbon neutrality". Electrocatalytic CO₂RR is complex as it involves multiple electron/proton transfer processes. The reaction mechanism is also complex and involves many intermediates, which ultimately affects product selectivity. The large-scale application of the CO₂RR requires the development of cheap and efficient electrocatalysts. Atomically dispersed metal and nitrogen co-doped carbon (M-N-C) materials, with large surface areas, 100% atomic availability, unsaturated coordination, and relatively uniform active sites, are promising catalysts for the CO₂RR. M-N-C materials also have adjustable properties. For example, tuning the coordination environment of the central metal ions changes the electronic properties and atomic structures of the metal ions, which provides a new way for designing catalysts with high CO₂RR performances. Therefore, it is of great significance to investigate the effect of regulating the electronic structure of M-N-C materials at the atomic level on catalytic activity and selectivity during the CO₂RR. Additionally, the reduction potentials of the half reactions of most CO₂RR products are within ±0.2 V of the hydrogen evolution reaction (HER), and most catalysts that bind CO₂ are rich in electrons and active for the HER. Therefore, it is also necessary to design catalysts that can kinetically inhibit the competitive HER during the CO₂RR. In this review, we discuss the synthesis methods of M-N-C materials, the reaction pathways of CO₂ reduction to C1, C2, and C2+ hydrocarbons, and the main factors affecting the CO₂RR. Specifically, three strategies for regulating the electronic structures and geometric configurations of M-N-C materials are systematically reviewed, namely, the modification of the carbon base surface of M-N-C materials, selection of appropriate central metal ions, and regulation of the coordination environment of the central metal ions. The effects of different active sites on the selectivity towards various products during the catalytic CO₂RR are also discussed in detail. Finally, we highlight the current challenges and future development directions of M-N-C materials for the electrocatalytic CO₂RR.

Key words: M-N-C material, Single-atom catalyst, Electronic structure, Coordination environment, Gibbs free energy

Tianmi Tang, Zhenlu Wang, Jingqi Guan. Electronic Structure Regulation of Single-Site M-N-C Electrocatalysts for Carbon Dioxide Reduction[J]. Acta Phys. -Chim. Sin. 2023, 39(4), 2208033. doi: 10.3866/PKU.WHXB202208033

Figures/Tables 13

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Table 1

Comparison of CO2RR performance of M-N-C catalysts."

Catalyst	Active site	Electrolyte	Product	FE (%)	TOF	Ref.
Fe/NG	Fe—N₄	0.1 mol∙L⁻¹ KHCO₃	CO	80	–	37
Fe-N-C	Fe—N₄	0.1 mol∙L⁻¹ KHCO₃	CO	91	–	55
Fe-N-C	Fe—N	0.1 mol∙L⁻¹ KHCO₃	CO	65	–	105
FeSAs/CNF-900	Fe—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	86.9	639 h⁻¹	50
Fe³⁺-N-C	Fe—N_x	0.5 mol∙L⁻¹ KHCO₃	CO	95	–	123
Fe-N-C	Fe—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	94	0.13 s⁻¹	124
Fe-N₄/CF	Fe—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	94.9	–	125
Fe-N-C	Fe—N₂₊₂−C₈	0.5 mol∙L⁻¹ KHCO₃	CO	93	–	126
Co₁-N₄	Co—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	82	1455 h⁻¹	127
Co-N₂ sample	Co—N₂	0.5 mol∙L⁻¹ NaOH	CO	94	33000 h⁻¹	44
CoPc-1	Co—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	94	0.29 s⁻¹	128
CoCoPCP/CNTs	Co—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	94	2.4 s⁻¹	35
CoTPP-CNT	Co—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	> 90	2.75 s⁻¹	129
CoPc-CN	Co—N₄	0.1 mol∙L⁻¹ NaHCO₃	CO	96	4.1 s⁻¹	36
CoFPc	Co—N₄	0.5 mol∙L⁻¹ NaHCO₃	CO	93	2.1 s⁻¹	130
CoPPc/CNT	Co—N₄	0.5 mol∙L⁻¹ NaHCO₃	CO	90	4900 h^-1	131
CoPc-MWCNT	Co—N₄	0.5 mol∙L⁻¹ KHCO₃	CH₃OH	19.5	–	132
CoPc2	Co—N₄	0.5 mol∙L⁻¹ NaHCO₃	CO	95	2.7 s⁻¹	133
Co-N₅/HNPCSs	Co—N₅	0.2 mol∙L⁻¹ NaHCO₃	CO	99	480.2 h⁻¹	134
CoPc	Co—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	99	–	135
Ni-N-C	Ni—N	0.1 mol∙L⁻¹ KHCO₃	CO	85	–	105
Ni-NG	Ni—N	0.5 mol∙L⁻¹ KHCO₃	CO	95	2.1 × 10⁵ s⁻¹	136
A-Ni-NG	Ni—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	97	14800h⁻¹	137
NC-CNTs(Ni)	Ni—N₃	0.1 mol∙L⁻¹ KHCO₃	CO	90	12000 h⁻¹	138
Ni SAs/N-C	Ni—N₃	0.5 mol∙L⁻¹ KHCO₃	CO	71.9	5273 h⁻¹	139
Cu-N-C-900	Cu—N	0.1 mol∙L⁻¹ KHCO₃	CH₄	38.6	–	27
Cu-N-C-800	Cu—N₂	0.1 mol∙L⁻¹ KHCO₃	C₂H₄	24.8	–	27
CuPc	Cu—N₄	0.5 mol∙L⁻¹ KHCO₃	CH₄	66	–	140
CuZnDTA	Cu—N₂	0.5 mol∙L⁻¹ KHCO₃	CH₃OH	54.8	–	141
CuSAs/TCNFs	Cu—N₄	0.1 mol∙L⁻¹ KHCO₃	CH₃OH	44	–	114
CuZnDTA	Cu—N₂	0.2 mol∙L⁻¹ KHCO₃	C₂H₅OH	31.4	–	141
Cu-N-C	Cu—N₄	0.1mol∙L⁻¹ CsHCO3	C₂H₅OH	55	–	79
ZIF-8	Zn—N	0.25 mol∙L⁻¹ K₂SO₄	CO	81.0	–	142
SA-Zn/MNC	Zn—N₄	1 mol∙L⁻¹ KHCO₃	CH₄	85	–	143
Zn-N-G-800	Zn—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	91	–	144
ZnN_x/C	Zn—N₄	0.5 mol∙L⁻¹ KHCO₃	CO	95	9969 h⁻¹	145
Sn^δ+/NG	Sn—N	0.25 mol∙L⁻¹ KHCO₃	HCOOH	74.3	11930 h⁻¹	120
Sn-CF	Sn—N	0.1 mol∙L⁻¹ KHCO₃	CO	91	–	72
Sb SA/NC	Sb—N₄	0.5 mol∙L⁻¹ KHCO₃	HCOOM	94	–	122

Table 1

Fig 9

Fig 10

Fig 11

Fig 12

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Electronic Structure Regulation of Single-Site M-N-C Electrocatalysts for Carbon Dioxide Reduction

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