Recent advances in charge mechanism of noble metal-based cathodes for Li-O<sub>2</sub> batteries

Recent advances in charge mechanism of noble metal-based cathodes for Li-O₂ batteries

PDF

Yong Zhao^*^,^a, Wei Cheng^b, Jiahan Wu^a^,^c, Zhengguang Hu^a, Fengliang Liu^a, Li Wang^*^,^a^,^c, Honggen Peng^*^,^d

Chinese Chemical Letters | 2023, 34(2) : 107413

Less

Chinese Chemical Letters | 2023, 34(2): 107413

• Review •

Recent advances in charge mechanism of noble metal-based cathodes for Li-O₂ batteries

Full

Yong Zhao^*^,^a, Wei Cheng^b, Jiahan Wu^a^,^c, Zhengguang Hu^a, Fengliang Liu^a, Li Wang^*^,^a^,^c, Honggen Peng^*^,^d

Affiliations

^a Department of Physics, Nanchang University, Nanchang 330031, China

^b Xiang Yang Public Inspection and Testing Center, Xiangyang 441000, China

^c Institute for Advanced Study, Nanchang University, Nanchang 330031, China

^d Key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, School of Resources Environmental and Chemical Engineering, Nanchang University, Nanchang 330031, China

Published: 2023-02-15 doi: 10.1016/j.cclet.2022.04.011

Outline

Abstract

Less

Lithium-oxygen (Li-O₂) batteries are considered as the next generation for energy storages systems due to the higher theoretical energy density than that of Li-ion batteries. However, the high charge overpotential caused by the insulated Li₂O₂ results in low energy efficiency, side reaction from electrolyte and cathode, and therefore poor battery performance. Designing noble metal-based catalysts can be an effective strategy to develop high-performance Li-O₂ batteries with low charge overpotentials and outstanding cycle stability. However, the charge mechanism for noble metal-based catalysts is not clear and even contradictory. Herein, several charge mechanisms of Li₂O₂ are first discussed. Subsequently, the possible charge processes of Li-O₂ batteries with noble metal-based catalysts are illustrated. In addition, the future development for noble metal-based catalysts is outlined.

Key words

Li-O₂ batteries / Noble metals / Charge overpotentials / Adsorption energy

Cite this Article

Yong Zhao, Wei Cheng, Jiahan Wu, Zhengguang Hu, Fengliang Liu, Li Wang, Honggen Peng. Recent advances in charge mechanism of noble metal-based cathodes for Li-O₂ batteries[J]. Chinese Chemical Letters, 2023 , 34 (2) : 107413 - . DOI: 10.1016/j.cclet.2022.04.011

Full Text

Less

1 Introduction

Less

Compared to Li-ion batteries, metal-air batteries show the higher energy densities [1-3], demonstrating great potential for energy storage systems [4-8]. Rechargeable lithium-oxygen (Li-O₂) batteries have attracted wide attention due to high theoretical energy density (3500 Wh/kg) that originates from the reversible reaction of lithium peroxide [9-12]. Traditionally, Li-O₂ cells are composed of the Li anode, separator and cathode catalyst [13-20]. According to different electrolytes, batteries can be divided into four categories: non-aqueous, aqueous, hybrid, all-solid-state electrolytes [18, 21-24]. A non-aqueous Li-O₂ battery includes a lithium foil anode, a cathode electrode and the nonaqueous electrolytes, where the lithium salts are dissolved in nonaqueous electrolyte. For aprotic Li-O₂ cells, Li is oxidized to Li⁺ during discharge process, while O₂ is dissolved in the solvent to react with Li⁺ and generate Li₂O₂ [24-29]. For the charge process, the insulating Li₂O₂ is decomposed to generate Li⁺ and O₂ [30-32]. However, the porous cathodes are seriously passivated by the insulating discharge products (Li₂O₂). To address the passivation issues, the Li-O₂ batteries with aqueous the electrolytes are proposed [33]. Different from the non-aqueous Li-O₂ batteries, the discharge product of aqueous Li-O₂ batteries is LiOH, which can enhance the conductivities of discharge products, thereby promoting the electrochemical performances. To inhibit the direct contact between the lithium anode and the aqueous electrolytes, a hybrid non-aqueous/aqueous system is further proposed, which can improve the stability and durability of Li-O₂ batteries [34]. Actually, the aforementioned non-aqueous, aqueous and hybrid electrolytes are based on the liquid solvents which can cause the safety issues and result in low energy densities. To improve the safety and energy densities, a variety of solid-state solvents containing polymers and inorganic solid electrolyte are utilized in Li-O₂ batteries [35]. Though different kinds of Li-O₂ batteries show huger potential than that of Li-ion batteries, the commercialization of Li-O₂ cells is always impeded by various barriers including low energy efficiency, inferior cycle performances and unavoidable side reactions from electrolytes and cathodes [36-39]. Especially, the high charge overpotentials caused by the insulated Li₂O₂ can cause the degradation of solvents and electrodes, and therefore leading to poor performances [40-46]. To alleviate the high charge overpotentials, various catalysts such as carbon materials [46-52], transition metal oxides [53-61], perovskites [37, 62-65] and noble metals [66-69] are utilized to accelerate the oxidation of Li₂O₂. Among the cathode catalysts, due to half-filled antibonding states, noble metal-based catalysts are regarded as a promising catalysts for Li-O₂ batteries, which can tune adsorption strength towards intermediates [70]. However, the charge mechanism of Li-O₂ cells with noble metals has not been elucidated clearly. For instance, Byon et al. revealed that noble metal could simultaneously facilitate the oxidation of solvents and discharge products [30]. Therefore, the cycle performance cannot be obviously enhanced. In comparison, Kang et al. proposed that the anisotropic Pt would facilitate the generation and oxidation of Li₂O₂, delivering enhanced OER catalytic activities compared to commercial Pt/C catalysts [71]. Therefore, a comprehensive understanding of the oxidation mechanism is essential to rationally design efficient noble metal catalysts for promoting the oxidation of discharge products at low charge overpotentials.

Herein, we summarize the recent progress of charge mechanisms for noble metal-based Li-O₂ cells. We begin the review by highlighting the different charge mechanisms of Li₂O₂. Subsequently, the charge processes of various noble metals are discussed. Finally, we conclude the current charge mechanisms of high-performance Li-O₂ batteries and the future direction for constructing reasonable noble metal catalysts.

2 Charge mechanism for Li₂O₂

Less

Several charge mechanisms are proposed for Li-O₂ batteries, including one electron oxidation and two-electron oxidation. Bruce et al. showed that the oxidation of Li₂O₂ is conducted via a two-electron oxidation process since no O₂⁻ or LiO₂ can be detected via the surface enhanced Raman spectroscopy (SERS) [72]. In contrast, Yang et al. [73] believed that the oxidation process of Li₂O₂ may contain several steps (Fig. 1a). In the sloping region with low charge overpotential, the oxidation with the formation of Li-deficient products (Li_2-xO₂) is attributed to both the one-electron solid-solution-like delithiation and the continuous removal of particles or discs in different surface regions. The two-phase oxidation process of bulk Li₂O₂ can be identified at high voltage plateau (E = 3.4 V). Yang et al. [73] showed that the lithium superoxide (LiO₂) can be generated at low charge overpotentials due to one-electron oxidation of Li₂O₂, followed by disproportionation reactions of LiO₂, while oxidation of bulk Li₂O₂ via two-electron process appears at high charge voltages (Fig. 1b). Furthermore, similar results can also be achieved by Marnix et al. [74]. They demonstrated that the non-crystalline peroxide is first charged during initial charge stage, then the crystalline peroxide is charged at high charge voltage to generate Li-deficient solid solution phase (Li_2-xO₂) via one-electron oxidation (Figs. 1c and d) [75]. The existence of LiO₂ is confirmed by Lu et al. [76]. They claimed that the soluble LiO₂ could be generated during oxidation process of Li₂O₂ in high donor number solvents, while LiO₂ is absent and Li_2-xO₂ can be formed in low-donicity solvent (Fig. 1e). The existence of LiO₂ is further confirmed by the thin-film rotating ring-disk electrode (RRDE) and X-ray absorption near-edge spectrum.

In addition, the different morphologies of Li₂O₂ also reflects distinctive mechanisms. For the toroid-shape discharge products, electron transportation from toroidal Li₂O₂ to current collectors is difficult due to the poor electronic conductivity [77]. At a low charge potential, lithium-deficient product (Li_2-xO₂) is formed, followed by the oxidation process of Li_2-xO₂ at a relatively plat voltage area. With the continuous charge process, oxidation of byproducts and solvents occurs at high charge overpotentials according to the previous reports [73, 78]. In contrast, for the Li₂O₂ thin films, the electron transport can be realized by the electron tunneling through the film (with thickness of 5–10 nm) [79]. Additionally, the Li₂O₂ thin films are amorphous compared to crystalline Li₂O₂ with toroid shapes [23, 80-82]. Peng et al. [80] also stated that the amorphous Li₂O₂ shows two to three orders of magnitude higher in ionic and electronic conductivity than that of commercial Li₂O₂, leading to a low charge overpotential. Therefore, the charge overpotential of amorphous Li₂O₂ thin films is low due to enhanced electronic conductivities compared to that of toroidal Li₂O₂. Another reason for the low charge overpotential of Li₂O₂ films is ascribed to the increased contact interfaces between Li₂O₂ films and cathodes [29, 83]. Though the Li₂O₂ thin film can be decomposed at a low voltage, the disadvantages of Li₂O₂ thin film including low discharge capacity and seriously parasitic reactions should be considered. In the future, efficient catalysts should be designed to balance the capacity and charge overpotentials [39, 41, 84].

3 OER mechanisms for noble metal-based cathodes

Less

3.1 OER for noble metals

Noble metals have attracted increasing attention since they can provide the ideal adsorption sites and strength for Li₂O₂ [71, 85-92]. The gold cathode by Peng et al. [87] displayed the reversible generation and oxidation of Li₂O₂ for 100 cycles, which inspires the development of noble metal-based cathodes in Li-O₂ cells (Fig. 2a). Yang et al. [93] showed that the ORR activity of Pd, Au, Pt and Ru established a volcano-shaped regulation, which is in consistent with the trend in fuel cell batteries (Fig. 2b). Among all the noble metals, Ru demonstrates superior catalytic activity for OER performances. Zhou et al. [94] stated that Ru@MWCNTP-based catalysts exhibit a lower charge overpotential of 0.68 V than that of MWCNTP cathode (1.04 V); Jeong et al. [95] investigated the catalytic effect of Ru, Pd and Au on the reduced graphene oxide during charge process. They claimed that the Ru-reduced oxide graphene (Ru-rGO) composite displays low charge overpotential compared to the other noble metal since the Ru nanoparticles can induce Li₂O₂ thin films.

The surface structure of noble metals will have an effect on the charge overpotentials. Kang et al. [71] stated that the anisotropic Pt catalyst with high-index (411) facets show superior OER performances with low overpotential (0.51 V) at 0.2 A/g (Fig. 2c). According to the calculation results (Fig. 2d), the principal reason is the higher activity of the high-index facets than that of the low-index facets. Meanwhile, Su et al. [96] showed that Au nanocrystals with high-index facets displayed higher excellent OER activities than the Au with low-index facets. They believed that the excellent activity performance of high-index facets is due to the high surface energy, which can enhance the interaction between O and Li atoms, thereby facilitating the decomposition of Li₂O₂.

Due to the intrinsic affinity towards LiO₂, noble metals can inhibit the formation of Li₂O₂, leading to the generation of LiO₂ as the main discharge products. For example, Lu et al. [86] designed a suitable noble metal-based cathode that contains Ir and reduced oxide graphene (rGO) for Li-O₂ batteries (Figs. 3a and b). LiO₂ is detected as the main discharge products by the XRD patterns and Raman spectra (Figs. 3c and d). Another evidence for the formation of LiO₂ is the discharge curves of LiO₂ under Ar atmosphere. After LiO₂ was discharged at 1000 mAh/g (the red curves in Fig. 3e), the crystalline LiO₂ can be formed. This result suggested that LiO₂ can be formed by a one-electron process with a capacity of 1000 mAh/g (Fig. 3f). They believed the lattice matching degree between LiO₂ and Ir₃Li determined the generation of LiO₂. Since the disproportionation reaction rate of Li₂O₂ is determined by the two factors: (1) the desorption rate of O₂ from the LiO₂ surface; (2) the solvent effect, the electrolytes can prevent LiO₂ from disproportionation and bring good stability of crystalline LiO₂. This research work provides new directions for designing defective discharge products to inhibit side reactions by lattices matching between catalysts and discharge products.

Apart from the noble metal cluster, the noble-metal single-atom catalysts (NMSACs) with well-defined structures can enhance the catalytic activities by increasing the active sites. Recently, Hu et al. [69] developed Ru single-atom onto nitrogen-doped porous carbon (Ru_0.1 SAs-NC and Ru_0.3 SAs-NC) as cathode catalysts for Li-O₂ batteries. Compared to the ZIF-8, Ru_0.3 SAs-NC demonstrates a low adsorption strength towards LiO₂ and Li₂O₂ (Figs. 4a-f). Furthermore, the Gibbs free energy profiles demonstrates that the rate determining step for ORR and OER processes are the reduction of O₂ to form Li₂O₂ clusters and the oxidation of Li₂O₂ clusters to generate O₂, respectively. Due to the weak binding interaction towards LiO₂, Ru_0.3 SAs-NC delivers a low discharge polarization (2.34 V in Fig. 4g). The charge density difference further confirms an abundant electron transfer for the Ru_0.3 SAs-NC (Fig. 4h). Meanwhile, compared to the pyrolyzed ZIF-8, the density of state (DOS) suggested that Ru mainly contributed to DOS below the Fermi level of the Ru_0.3SAs-NC (Figs. 4i and j), indicating the superior catalytic activities.

As discussed in detail above, though the noble metal can decrease the charge polarizations and enhance the energy efficiency in Li-O₂ batteries, using noble catalysts also increases the risk of side reactions from cathodes and electrolytes. For instance, Pt and Pd based catalysts can accelerate the decomposition of solvent by the differential electrochemical mass spectrometry (DEMS) results [95, 97]. Peng et al. [85] showed that the continuous CO₂ evolution can be identified at the later charge process for Ru-carbon nanotube (Ru-CNT) and Pd-CNT catalysts by the DEMS characterizations (Figs. 5a and b). Though Ru-CNT and Pd-CNT catalysts can improve OER overpotentials and high round-trip efficiency (Figs. 5c and d), the reversibility is impaired by the parasitic reactions. Therefore, there is no improvement for the rechargeability by using Ru-CNT and Pd-CNT cathodes (Figs. 5e and f). Similar results was observed by Byon et al. [30]. By using Pt, Ru, Pd and Au as cathode catalysts for Li-O₂ cells, they found that the oxidation process of Li₂O₂ is accompanied by more side reaction. These results suggest that using noble metal-based catalysts in fact damage the reversible formation and decomposition of Li₂O₂.

3.2 OER for noble metal oxides

Among all the noble metal oxides, RuO₂ represents excellent OER catalytic performances due to its metallic character with high electronic conductivity (10⁴ S/cm for single crystal) [98, 99]. Zhou et al. [100] prepared the RuO₂ hollow spheres with diameters of 200–300 nm as the catalyst for cathode electrodes. The RuO₂ hollow spheres showed a charge overpotential of only 0.54 V even up to 100 cycles. Impressively, Zhou et al. [88] also designed a core shell-structured CNT@RuO₂ hybrid as the cathode. The Li-O₂ batteries with CNT@RuO₂ cathodes showed a low charge overpotential of 0.51 V. Unfortunately, the specific role of RuO₂ during the OER process should be further elucidated. Byon et al. suggested that the RuO₂ was beneficial to the generation of amorphous Li₂O₂ on the CNTs, and the large contact area between CNTs and Li₂O₂ can promote the OER kinetics (Figs. 6a and b) [101]. According to first-principle calculations, Kim et al. [102] proposed that insulated Li₂O₂ can interact with RuO₂ through a Stranski-Krastanov growth mode and transform into conductive Li₂O₂, which leads to a low charge overpotential. RuO₂ demonstrates strong adsorption strength towards Li₂O₂ (−3.74 eV), leading to the formation of RuO₂/Li₂O₂ heterostructure. After depositing Li₂O₂ on the surface of RuO₂, obvious charge transfer as well as remarkable lattice mismatch between Li₂O₂ and RuO₂ can be observed (Fig. 6c), which makes the insulative Li₂O₂ conductive according to the density of state results (Fig. 6d). Recently, the charge mechanism of RuO₂ was further investigated by Chen's group [103] via an aberration-corrected scanning transmission electron microscope with a high angle annular dark field detector (HAADF-STEM) and synchronous electrochemical measurements. During the charge process, the catalytic sites are located at solvent-RuO₂-Li₂O₂ triple-phase interfaces. RuO₂ can accelerate both the oxidation process of surfaced discharge products and the decomposition of soluble LiO₂ to dissolve the insulated discharge product of Li₂O₂ via a chemical disproportionation reaction. This mechanism provides new insights into OER reactions of noble metal-based catalysts.

3.3 OER for noble metal-based alloys

Alloying noble metal with the other metal is a feasible tactic to enhance the catalytic performance for Li-O₂ batteries. Considering Pt-based alloy, Shao Horn et al. [104] developed PtAu nanoparticles as the catalyst for Li-O₂ cells, resulting in a low overall potential (0.85 V) at 0.05 A/g (Figs. 7a and b). In addition, the PdCu nanoparticles fabricated by Kang et al. [90] demonstrate a high energy efficiency of 80% at 0.2 A/g. The DFT calculations showed that the electron transfer from Cu to Pd can decrease adsorption strength towards LiO₂, leading to a low OER overpotential (Figs. 7c and d). Similarly, Kim et al. [91] confirmed that the adsorption strength towards LiO₂ is related to the charge overpotential of Pt₃Co catalysts. In particular, the decreased adsorption between LiO₂ and Pt₃Co alloy caused a low charge overpotential of 0.56 V at 0.2 A/g.

Similar results were also reported by Guo et al. [105], where the PtIr alloys are rationally designed as the efficient catalysts for Li-O₂ batteries. Pt atom with high electronegativity tends to capture electron from Ir atoms, leading to lower Lewis acidity of Pt atoms and thereby causing the downshift of d-band center (Figs. 8a-c). which results in the weaker adsorption strength towards LiO₂ (−2.50 eV) compared to pure Pt (Fig. 8c). The weak binding interaction between LiO₂ and PtIr alloys bring about the outstanding discharge (0.60 V) and charge (1.16 V) catalytic activities (Figs. 8d and e). The Gibbs free energy profiles show that the rate determining steps for discharge and charge processes are the formation of 2LiO₂ molecules and the oxidation of LiO₂ to release O₂, respectively.

Another tactic to enhance the electrochemical performances of noble metals is tuning the shape of noble metal-based alloys, which can provide abundant exposed ledges and atomic steps. Kang et al. [106] fabricated Pt₃Co nanocubes (NCs) surrounded by (100) planes and 12 edged surfaces (Figs. 9a and b). Compared to Pt₃Co nanoparticles, Pt₃Co nanocubes delivered a high energy efficiency and excellent rate performances (Figs. 9c and d). The enhanced performance of Pt₃Co nanocubes was ascribed to the electronic structure, atomic arrangement and the cubic morphologies.

3.4 OER for noble metals and transition-metal oxides hybrids

Noble metals and transition-metal oxides hybrids are effective catalysts, which can promote the formation and oxidation of discharge products. Among them, Ru or RuO₂ based hybrid catalysts demonstrates excellent ORR and OER performances. Zhou et al. [107] utilized Ru/MnO₂ as the cathode for Li-O₂ batteries with water as the protic additives in aprotic electrolytes. During the discharge process, LiOH and H₂O₂ were generated by the reaction between Li₂O₂ and H₂O. During the charge process, H₂O₂ can convert into H₂O and O₂ due to the catalytic effect of MnO₂ while LiOH can be oxidized by Ru noble metals, leading to low charge overpotentials (0.21 V). As a result, Li-O₂ batteries with Ru/MnO₂ cathodes showed outstanding OER and rate performances. Meanwhile, the catalytic role of Ru/MNT was investigated by Zhu et al. with the help of operando synchrotron radiation powder X-ray diffraction (SR-PXD in Figs. 10a-c) [108]. The oxidation of Li₂O₂ on the Ru/MNT cathodes follows a pseudo-zero-order kinetics, therefore, the Ru/MNT cathode delivers a coulombic efficiency of 100% (Fig. 10d).

Additionally, Dong et al. [92] developed α-MnO₂/RuO₂ as the catalyst for Li-O₂ batteries. The synergistic catalytic mechanism between α-MnO₂ and RuO₂ was proposed. During the charge process, more LiO₂ can be generated on the α-MnO₂/RuO₂ cathodes compared to that of pure RuO₂ electrodes. In detail, Li ions and Li_2−xO₂ can be stabilized by α-MnO₂ and RuO₂, respectively. Subsequently, the Li_2−xO₂ could be easily decomposed by RuO₂ (Fig. 11a). Therefore, the Li-O₂ batteries with α-MnO₂/RuO₂@CN cathodes show good rate performances and excellent cycle performances (45 cycles) with a low charge overpotential (0.25 V). The synergistic charge mechanism provides a novel strategy to obtain high-performance Li-O₂ batteries (Figs. 11b-d).

4 Conclusion

Less

In this review, we mainly discuss the recent progress of the charge mechanisms for the noble metal-based catalysts in Li-O₂ batteries. The noble metal-based cathodes contain noble metals, noble metal oxides, noble metal-based alloy, and noble-transition metal oxides hybrids. The oxidation of discharge products can be a one-electron or two-electron process, which is determined by the solvents and catalysts. For the noble metal cathodes, the charge overpotential can be decreased by the high-index facets or the formation of other types of discharge products, which can enhance the electrochemical performances. In comparison, it is suggested that the noble metals could also lead to the degradation of solvents, bringing negligible improvement for the cycle performances. For the noble metal oxides in Li-O₂ batteries, during the charge process, the oxidation of Li₂O₂ can be promoted by the interaction between Li₂O₂ and catalysts by constructing the solvent-catalyst-Li₂O₂ triple-phase interfaces. For the catalytic activity of noble metal-based alloy, the electron properties and the shape of alloys can affect the decomposition process of Li₂O₂. In the last section, the OER mechanisms of noble-transition metal oxides hybrids were elucidated. OER is a complicated process, which contains multistep electrochemical reactions. The OER process can be influenced by many parameters such as high-index facets, shapes, and the composition of noble metals. Though remarkable progress has been made for the charge mechanisms in Li-O₂ batteries, substantial efforts should be devoted for a fundamental understanding of Li₂O₂ decomposition. The process of Li₂O₂ oxidation on the O₂ cathode during the charge process is always under debate. Therefore, the in situ characterizations should be established to provide direct evidence for the analysis of OER process.

Developing efficient noble metal cathodes with superior stability and high energy efficiency is the ultimate goal for high-performance Li-O₂ batteries. To obtain low OER overpotentials and excellent cycle performances, two strategies can be proposed: (1) maximizing noble metal atomic utilization by construing the noble metal single-atom catalysts, (2) decreasing the OER overpotentials by the strain engineering. Due to the high cost and low abundance of noble metals, decreasing the content of noble metals while maintaining high OER catalytic is urgent. Therefore, constructing the noble metal single-atom catalysts can show the maximum atom-utilization efficiency, leading to excellent OER performance [69]. In addition, the local environment, coordination number and spatial configuration of noble metal single atom can be modulated to further tune the electronic structure and determine the OER catalytic performance [109]. On the other hand, the OER activity of noble metals can be tuned by the strain effect, which includes the compressive and tensile strain. The strain can be generated by forming the core-shell structure, shape variation, alloys, grain boundaries, etc. [110]. Generally, tuning the lattice strain has already been confirmed to be effective in the electrocatalyst design. Usually, introducing a compressive strain can cause the downshift of d-band center for the noble metal with fixed d orbital occupancy. Therefore, the antibonding d states will move to a low energy level, which increases electron occupation and enhances adsorption strength towards intermediates [111]. In comparison, the tensile strain of noble metals induces the upshift of d-band center, enhancing the binding interaction between intermediates and catalysts. Therefore, the rate determining step during the ORR and OER process can be tuned by the strain engineering for the noble metal catalysts. With continuous efforts, the Li-O₂ batteries with high energy densities will show great commercial potential in the future.

Declaration of competing interest

Less

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgments

Less

The authors acknowledge the financial support from the National Natural Science Foundation of China (No. 12175098) and Hundred Talents Sailing Project of Jiangxi Province, China.

References

Less

[1]

X. Guo, S. Zheng, Y. Luo, H. Pang, Chem. Eng. J. 401 (2020) 126005.

[2]

B. Li, H. Xue, H. Pang, Q. Xu, Sci. China Chem. 63 (2020) 475–482.

[3]

B. Li, R. Zhu, H. Xue, J. Colloid. Interf. Sci. 563 (2020) 328–335.

[4]

S. Peng, H. Huang, D. Yu, Angew. Chem. Int. Ed. 61 (2022) e202116068.

[5]

D. Yu, Y. Ma, F. Hu, Adv. Energy Mater. 11 (2021) 2101242.

[6]

J. Song, S. Qiu, F. Hu, Adv. Funct. Mater. 31 (2021) 2100618.

[7]

D. Ji, L. Fan, L. Li, Adv. Mater. 31 (2019) 1808267.

[8]

L. Deng, F. Hu, M. Ma, Angew. Chem. Int. Ed. 60 (2021) 22276–22282.

[9]

D. Aurbach, B.D. McCloskey, L.F. Nazar, P.G. Bruce, Nat. Energy 1 (2016) 16128.

[10]

W. Dai, X. Cui, Y. Zhou, Small Methods 3 (2019) 1800358.

[11]

Y. Ko, H.I. Kim, S.J. Cho, Adv. Energy Mater. 11 (2021) 2102096.

[12]

Y. Bae, H. Song, H. Park, Adv. Energy Mater. 10 (2020) 1904187.

[13]

X. Gao, Y. Chen, L. Johnson, P.G. Bruce, Nat. Mater. 15 (2016) 882–888.

[14]

X. Gao, Y. Chen, L.R. Johnson, Nat. Energy 2 (2017) 17118.

[15]

Y. Ko, H. Park, K. Lee, Angew. Chem. Int. Ed. 132 (2020) 5414–5418.

[16]

D. Wang, F. Zhang, P. He, H. Zhou, Angew. Chem. Int. Ed. 131 (2019) 2377–2381.

[17]

H. Deng, Y. Qiao, X. Zhang, J. Mater. Chem. A 7 (2019) 17261–17265.

[18]

W.J. Kwak, J. Park, H. Kim, ACS Energy Lett. 5 (2020) 2122–2129.

[19]

F. Marques Mota, J.H. Kang, Y. Jung, Adv. Energy Mater. 10 (2020) 1903486.

[20]

M. Hong, C. Yang, R.A. Wong, J. Am. Chem. Soc. 140 (2018) 6190–6193.

[21]

N. Feng, P. He, H. Zhou, Adv. Energy Mater. 6 (2016) 1502303.

[22]

W.J. Kwak, S.J. Park, H.G. Jung, Y.K. Sun, Adv. Energy Mater., 8 (2018) 1702258.

[23]

R.A. Wong, A. Dutta, C. Yang, Chem. Mater. 28 (2016) 8006–8015.

[24]

J.B. Park, S.H. Lee, H.G. Jung, Adv. Mater. 30 (2018) 1704162.

[25]

A. Dutta, R. Wong, W. Park, Nat. Commun. 9 (2018) 680.

[26]

Z. Qian, X. Li, B. Sun, J. Phys. Chem. Lett. 11 (2020) 7028–7034.

[27]

J. Zhang, B. Sun, Y. Zhao, Angew. Chem. Int. Ed. 56 (2017) 8505–8509.

[28]

J. Zhang, B. Sun, A.M. McDonagh, Energy Storage Mater. 7 (2017) 1–7.

[29]

C. Yang, R.A. Wong, M. Hong, Nano Lett. 16 (2016) 2969–2974.

[30]

R. Wong, C. Yang, A. Dutta, ACS Energy Lett. 3 (2018) 592–597.

[31]

W.J. Kwak, H.G. Jung, D. Aurbach, Y.K. Sun, Adv. Energy Mater. 7 (2017) 1701232.

[32]

H.J. Shin, W.J. Kwak, D. Aurbach, Y.K. Sun, Adv. Funct. Mater. 27 (2017) 1605500.

[33]

L. Puech, C. Cantau, P. Vinatier, J. Power Sources 214 (2012) 330–336.

[34]

E. Yoo, H. Zhou, ACS Nano 5 (2011) 3020–3026.

[35]

Y. Sun, Nano Energy 2 (2013) 801–816.

[36]

W.J. Kwak, J. Park, T.T. Nguyen, J. Mater. Chem. A 7 (2019) 3857–3862.

[37]

D.A. Agyeman, Y. Zheng, T. -. H. Lee, ACS Catal. 11 (2020) 424–434.

[38]

K. Adpakpang, S.M. Oh, D.A. Agyeman, Adv. Funct. Mater. 28 (2018) 1707106.

[39]

Z. Lyu, Y. Zhou, W. Dai, Chem. Soc. Rev. 46 (2017) 6046–6072.

[40]

Z. Huang, J. Ren, W. Zhang, Adv. Mater. 30 (2018) 1803270.

[41]

P. Zhang, Y. Zhao, X. Zhang, Chem. Soc. Rev. 47 (2018) 2921–3004.

[42]

B. Tong, J. Huang, Z. Zhou, Z. Peng, Adv. Mater. 30 (2018) 1704841.

[43]

W.B. Luo, X.W. Gao, S.L. Chou, Adv. Energy Mater. 7 (2017) 1700234.

[44]

T.H. Gu, D.A. Agyeman, S.J. Shin, Angew. Chem. Int. Ed. 57 (2018) 15984–15989.

[45]

X. Bi, M. Li, C. Liu, Angew. Chem. Int. Ed. 59 (2020) 22978–22982.

[46]

T. Zhao, Y. Yao, Y. Yuan, Nano Energy 82 (2021) 105782.

[47]

J. Shui, Y. Lin, J.W. Connell, ACS Energy Lett. 1 (2016) 260–265.

[48]

B. Sun, S. Chen, H. Liu, G. Wang, Adv. Funct. Mater. 25 (2015) 4436–4444.

[49]

Z. Zhang, J. Bao, C. He, Adv. Funct. Mater. 24 (2014) 6826–6833.

[50]

D. Cao, Y. Bai, J. Zhang, Nano Energy 89 (2021) 106464.

[51]

H. Xia, Q. Xie, Y. Tian, Nano Energy 84 (2021) 105877.

[52]

M. Tian, C. Wei, Z. Sun, Carbon N Y 178 (2021) 436–442.

[53]

J. Li, M. Zou, W. Wen, J. Mater. Chem. A 2 (2014) 10257–10262.

[54]

L. Ma, N. Meng, Y. Zhang, F. Lian, Nano Energy 58 (2019) 508–516.

[55]

L. Dai, Q. Sun, L. Chen, Nano Res. 13 (2020) 2356–2364.

[56]

R. Bi, G. Liu, C. Zeng, Small 15 (2019) 1804958.

[57]

J. Li, Y. Deng, L. Leng, J. Power Sources, 450 (2020) 227725.

[58]

Z.L. Jiang, G. -. L. Xu, Z. Yu, Nano Energy 64 (2019) 103896.

[59]

Y. Zheng, R. Gao, L. Zheng, ACS Catal. 9 (2019) 3773–3782.

[60]

X. Liu, L. Zhao, H. Xu, Adv. Energy Mater. 10 (2020) 2001415.

[61]

Y. Zhang, M. Hu, M. Yuan, Nano Res. 12 (2019) 299–302.

[62]

Y. Zhou, Q. Gu, Y. Li, Nano Lett. 21 (2021) 4861–4867.

[63]

M.C. Sung, G.H. Lee, D.W. Kim, InfoMat 3 (2021) 1295–1310.

[64]

X. Li, Z. Qian, G. Han, ACS Appl. Mater. Interfaces 12 (2020) 10452–10460.

[65]

Y. Cong, Z. Geng, Q. Zhu, Angew. Chem. Int. Ed. 133 (2021) 23568–23575.

[66]

T. Zhang, B. Zou, X. Bi, ACS Energy Lett. 4 (2019) 2782–2786.

[67]

Q. Huang, F. Dang, H. Zhu, J. Power Sources 451 (2020) 227738.

[68]

S. Hyun, A. Saejio, S. Shanmugam, Nanoscale 12 (2020) 17858–17869.

[69]

X. Hu, G. Luo, Q. Zhao, J. Am. Chem. Soc. 142 (2020) 16776–16786.

[70]

K. Song, D.A. Agyeman, M. Park, Adv. Mater. 29 (2017) 1606572.

[71]

K. Song, J. Jung, M. Park, ACS Catal. 8 (2018) 9006–9015.

[72]

T. Ogasawara, A. Débart, M. Holzapfel, J. Am. Chem. Soc. 128 (2006) 1390–1393.

[73]

B.M. Gallant, D.G. Kwabi, R.R. Mitchell, Energy Environ. Sci. 6 (2013) 2518–2528.

[74]

S. Ganapathy, B.D. Adams, G. Stenou, J. Am. Chem. Soc. 136 (2014) 16335–16344.

[75]

Y.C. Lu, Y. Shao-Horn, J. Phys. Chem. Lett. 4 (2013) 93–99.

[76]

Y. Wang, N.C. Lai, Y.R. Lu, Joule 2 (2018) 2364–2380.

[77]

F. Tian, M.D. Radin, D.J. Siegel, Chem. Mater. 26 (2014) 2952–2959.

[78]

B.M. Gallant, D.G. Kwabi, R.R. Mitchell, Energy Environ. Sci. 6 (2013) 2518–2528.

[79]

H.D. Lim, H. Song, H. Gwon, Energy Environ. Sci. 6 (2013) 3570–3575.

[80]

Y. Zhang, Q. Cui, X. Zhang, Angew. Chem. Int. Ed. 128 (2016) 10875–10879.

[81]

J. Lu, Y. Lei, K.C. Lau, Nat. Commun. 4 (2013) 1–10.

[82]

J. Hummelshøj, A. Luntz, J. Nørskov, J. Chem. Phys. 138 (2013) 034703.

[83]

J. Huang, B. Zhang, Z. Bai, Adv. Funct. Mater. 26 (2016) 8290–8299.

[84]

Y. Hu, X. Han, F. Cheng, Nanoscale 6 (2013) 177–180.

[85]

S. Ma, Y. Wu, J. Wang, Nano Lett. 15 (2015) 8084–8090.

[86]

J. Lu, Y. Lee, X. Luo, Nature 529 (2016) 377–382.

[87]

Z. Peng, S.A. Freunberger, Y. Chen, P.G. Bruce, Science 337 (2012) 563–566.

[88]

Z. Jian, P. Liu, F. Li, Angew. Chem. Int. Ed. 53 (2014) 442–446.

[89]

Y. Xing, N. Chen, M. Luo, Energy Storage Mater. 24 (2020) 707–713.

[90]

R. Choi, J. Jung, G. Kim, Energy Environ. Sci. 7 (2014) 1362–1368.

[91]

B.G. Kim, H. -. J. Kim, S. Back, Sci. Rep. 4 (2014) 1–9.

[92]

S. Cai, M. Zheng, X. Lin, ACS Catal. 8 (2018) 7983–7990.

[93]

Y.C. Lu, H.A. Gasteiger, Y. Shao-Horn, J. Am. Chem. Soc. 133 (2011) 19048–19051.

[94]

F. Li, Y. Chen, D. -. M. Tang, Energy Environ. Sci. 7 (2014) 1648–1652.

[95]

Y.S. Jeong, J.B. Park, H.G. Jung, Nano Lett. 15 (2015) 4261–4268.

[96]

D. Su, S. Dou, G. Wang, NPG Asia Mater. 7 (2015) e155.

[97]

B.D. McCloskey, R. Scheffler, A. Speidel, J. Am. Chem. Soc. 133 (2011) 18038–18041.

[98]

K. Liao, T. Zhang, Y. Wang, ChemSusChem 8 (2015) 1429–1434.

[99]

P. Bhattacharya, E.N. Nasybulin, M.H. Engelhard, Adv. Funct. Mater. 24 (2014) 7510–7519.

[100]

F. Li, D.M. Tang, T. Zhang, Adv. Energy Mater. 5 (2015) 1500294.

[101]

E. Yilmaz, C. Yogi, K. Yamanaka, Nano Lett. 13 (2013) 4679–4684.

[102]

J. Huang, Z. Jin, Z.L. Xu, Energy Storage Mater. 8 (2017) 110–118.

[103]

C. Hou, J. Han, P. Liu, Nano Energy 47 (2018) 427–433.

[104]

Y. -. C. Lu, Z. Xu, H.A. Gasteiger, J. Am. Chem. Soc. 132 (2010) 12170–12171.

[105]

Y. Zhou, K. Yin, Q. Gu, Angew. Chem. Int. Ed. 60 (2021) 26592–26598.

[106]

J. Jung, K. Song, Y. Bae, Nano Energy 18 (2015) 71–80.

[107]

F. Li, S. Wu, T. Zhang, Nat. Commun. 6 (2015) 1–7.

[108]

J. Liu, Y. Ma, M. Roberts, J. Power Sources 352 (2017) 208–215.

[109]

Z. Lei, W. Cai, Y. Rao, Nat. Commun. 13 (2022) 1–10.

[110]

X. Yang, Y. Wang, X. Tong, N. Yang, Adv. Energy Mater. 12 (2022) 2102261.

[111]

Z. Xia, S. Guo, Chem. Soc. Rev. 48 (2019) 3265–3278.

Appendix

Less

Year 2023 volume 34 Issue 2

PDF

Cite this Article

BibTeX

Article Info

doi: 10.1016/j.cclet.2022.04.011

Receive Date：2021-12-01
Online Date：2025-11-21
Published：2023-02-15

Article Data

Affiliations

History

Received：2021-12-01
Revised：2022-02-18
Accepted：2022-04-06

Affiliations

^a Department of Physics, Nanchang University, Nanchang 330031, China

^b Xiang Yang Public Inspection and Testing Center, Xiangyang 441000, China

^c Institute for Advanced Study, Nanchang University, Nanchang 330031, China

^d Key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, School of Resources Environmental and Chemical Engineering, Nanchang University, Nanchang 330031, China

References

Share

https://castjournals.cast.org.cn/joweb/ccl/EN/10.1016/j.cclet.2022.04.011

Share to

Scan QR to access full text

Cite this article

BibTeX

Citations

表12种不同金属材料的力学参数

科 Family	属数 Number of genus	种数 Number of species	占总种数比例 Percentage of total species (%)	属 Genus	种数 Number of species	占总种数比例 Percentage of total species (%)
鹅膏菌科Amanitaceae	2	11	5.26	鹅膏菌属 Amanita	10	4.78
小菇科 Mycenaceae	2	12	5.74	丝盖伞属 Inocybe	5	2.39
多孔菌科 Polyporaceae	8	14	6.70	蜡蘑属 Laccaria	5	2.39
红菇科 Russulaceae	3	23	11.00	小皮伞属 Marasmius	6	2.87
				小菇属 Mycena	11	5.26
				光柄菇属 Pluteus	5	2.39
				红菇属 Russula	17	8.13
				栓菌属 Trametes	5	2.39

关闭全屏

BibTeX
EndNote
RefWorks
TxT

Fig. 1. (a) The charge processes for Li₂O₂ with disk or particle morphologies. Reproduced with permission [73]. Copyright 2013, Royal Society of Chemistry. The charge processes of (b) E-Li₂O₂ and (c) C-Li₂O₂. Reproduced with permission [74]. Copyright 2014, American Chemical Society. (d) The proposed charge mechanisms of Li-O₂ batteries. Reproduced with permission [75]. Copyright 2013, Elsevier. (e) Proposed solvent-controlled Li₂O₂ decomposition mechanism. Reproduced with permission [76]. Copyright 2018, Elsevier.

Fig. 2. (a) The cycle performance of NPG cathodes. Reproduced with permission [87]. Copyright 2012, American Association for the Advancement of Science. (b) Nonaqueous Li⁺-ORR potentials as a function of calculated oxygen adsorption energy, ΔE_O, relative to that of Pt. Reproduced with permission [93]. Copyright 2011, American Chemical Society. (c) Discharge-charge curves for anisotropic Pt, Pt/C and KB carbon cathodes. (d) ORR and OER energy curves calculated on the Pt (411) planes. Reproduced with permission [71]. Copyright 2018, American Chemical Society.

Fig. 3. (a, b) TEM images of Ir-rGO catalysts. The circle in (b) shows some small Ir atomic clusters. Scale bars: (a) 10 nm, (b) 2 nm. (c) HE-XRD patterns of discharge product on Ir-rGO as a function of aging time. (d) Raman spectra of discharge products on Ir-rGO cathodes. (e) Voltage curves for Ir-rGO discharged first in O₂ and then in Ar at a capacity of 1000 mAh/g. (f) HE-XRD pattern of cathode resulting from both discharges in (e). Reproduced with permission [86]. Copyright 2016, Nature Publishing Group.

Fig. 4. The pristine (a) pyrolyzed ZIF-8 and (d) Ru_0.3 SAs-NC structures. The optimized structures of (b) LiO₂ adsorbed on pyrolyzed ZIF-8, (e) LiO₂ adsorbed on Ru-N₄ configuration of Ru_0.3 SAs-NC, and (c) Li₂O₂ adsorbed on pyrolyzed ZIF-8, (f) Li₂O₂ adsorbed on Ru-N₄ configuration of Ru_0.3 SAs-NC. (g) Gibbs free energy diagrams at 2.97 V for the discharge-charge reactions on the active surface of pyrolyzed ZIF-8, Ru_0.1 SAs-NC and Ru_0.3 SAs-NC. (h) Corresponding charge density distribution. Isosurface level = 0.002 a.u. The total density of states (DOS) and partial density of states (PDOS) of (i) pyrolyzed ZIF-8 and (j) Ru_0.1 SAs-NC. Reproduced with permission [69]. Copyright 2020, American Chemical Society.

Fig. 5. DEMS results for (a) Ru-CNT and (b) Pd-CNT catalysts during the charge process. (c) The first cycle of the pristine CNT, Ru-CNT and Pd-CNT cathodes. 100 cycles of Li-O₂ cells with (d) Ru-CNT and (e) Pd-CNT catalysts. (f) The terminal discharge voltage as a function of cycle number at a fixed capacity of 1000 mAh/g. Reproduced with permission [85]. Copyright 2015, American Chemical Society.

Fig. 6. The diagram of the discharge processes in (a) CNT and (b) RuO₂/CNT cathodes. Reproduced with permission [101]. Copyright 2013, American Chemical Society. (c) Charge density difference at the RuO₂ (110) slab. (d) Density of states (DOS) of (ⅰ) bulk RuO₂, (ⅱ) bulk Li₂O₂, (ⅲ) total DOS of RuO₂/Li₂O₂, (ⅳ) projected DOS (PDOS) of Ru, O and the adsorbed Li₂O₂. Reproduced with permission [102]. Copyright 2017, American Chemical Society.

Fig. 7. (a) TEM image of PtAu/C. (b) The first discharge/charge curves of Au/C, Pt/C, and PtAu/C for Li-O₂ batteries. Reproduced with permission [104]. Copyright 2010, American Chemical Society. Calculated energy diagrams for ORR and OER on (c) Pd(111) and (d) PdCu(111). Reproduced with permission [90]. Copyright 2014, Royal Society of Chemistry.

Fig. 8. (a) The Bader charge simulation for PtIr multipods. (b) The XPS spectra of Pt and PtIr catalysts in Pt 4f region. (c) The valence band spectra (VBS) of Pt and PtIr by UPS. The positions of the d-band centers were implied by short dashed lines. The insets are the adsorption energy of LiO₂ on the (111) planes of Pt and PtIr catalysts, respectively. (d, e) The Gibbs free energy at zero, equilibrium, discharge and charge voltages for Pt and PtIr cathodes. Asterisks denote the species absorbed on the surface of cathode catalysts. The insets in (d) and (e) are the optimized structures of the Pt and PtIr cathodes with adsorbates at corresponding charging steps. Reproduced with permission [105]. Copyright 2021, Wiley-VCH.

Fig. 9. TEM images of (a) Pt₃Co nanocubes and (b) nanoparticles. (c) The initial discharge-charge profiles between 2.0 V and 4.5 V at a current density of 200 mA/g_carbon. (d) The discharge profiles obtained at various current densities. Reproduced with permission [106]. Copyright 2015, Wiley VCH.

Fig. 10. (a-c) The structure of operando synchrotron radiation powder X-ray diffraction (SR-PXD). The left image in (b) is the SR-PXD sample holder with sample and the right one in (b) is the TEM image of that sample on the sample holder. (d) The profile of Li₂O₂ oxidation calculated from the charge capacity and SR-PXD, respectively. Reproduced with permission [108]. Copyright 2017, Elsevier.

Fig. 11. (a) The schematic illustration for the Li extraction from Li₂O₂ and migration on α-MnO₂/RuO₂ cathode. (b) The comparison of the discharge-charge curves between the α-MnO₂@GN RuO₂/GN, α-MnO₂@GN/RuO₂ and MRG electrode. (c) Discharge-charge profiles of MRG cathode at various current densities. (d) Voltage profiles of selected cycles at 100 mA/g for the MRG cathode. Reproduced with permission [92]. Copyright 2018, American Chemical Society.

Articles: Latest Articles; Most Read; Collections

Updates: Events; News; Multimedia

About: About Us

Contact

No. 86 Xueyuan South Road, Haidian District, Beijing

100081

010-62199257

qkjq@cast.org.cn

Copyright © 2025 China Association for Science and Technology. All rights reserved. For all open access content, the relevant licensing terms apply.
Sponsored by the Office of the Leading Group for Cybersecurity and Informatization of CAST, and supported by Science and Technology Review Publishing House