Electrolysis of water is regarded as an attractive and feasible way for producing hydrogen. So far, various non‐noble metal nanomaterials have been reported as excellent electrocatalysts for hydrogen evolution reaction. Especially, due to the low cost, earth‐abundance and tunable properties, transition metal selenides with different compositions, sizes and structures have been explored broadly as efficient catalysts with the relatively high activities, high stabilities and high efficiencies in full pH range of electrolyte for electrochemical hydrogen evolution reaction. Thus, in this Minireview, after introducing several commonly used electrochemical terms about hydrogen evolution reaction, we mainly focus on various kinds of the transition metal selenides that have been documented as electrocatalysts for hydrogen evolution reaction. Particularly, the merits and demerits of transition metal selenides for hydrogen evolution reaction are systematically discussed. Moreover, we also analyze the encountered challenges and present an outlook for the rapid development of transition metal selenides. We hope this Minireview can bring some fundamental understanding for the readers interested in the transition metal selenides and hydrogen evolution reaction.
Neurodevelopmental disorders are psychiatric diseases that are usually first diagnosed in infancy, childhood and adolescence. Autism spectrum disorder (ASD) is a neurodevelopmental disorder, characterized by core symptoms including impaired social communication, cognitive rigidity and repetitive behavior, accompanied by a wide range of comorbidities such as intellectual disability (ID) and dysmorphisms. While the cause remains largely unknown, genetic, epigenetic, and environmental factors are believed to contribute toward the onset of the disease. Autism Susceptibility Candidate 2 (Auts2) is a gene highly associated with ID and ASD. Therefore, understanding the function of Auts2 gene can provide a unique entry point to untangle the complex neuronal phenotypes of neurodevelpmental disorders. In this review, we discuss the recent discoveries regarding the molecular and cellular functions of Auts2. Auts2 was shown to be a key-regulator of transcriptional network and a mediator of epigenetic regulation in neurodevelopment, the latter potentially providing a link for the neuronal changes of ASD upon environmental risk-factor exposure. In addition, Auts2 could synchronize the balance between excitation and inhibition through regulating the number of excitatory synapses. Cytoplasmic Auts2 could join the fine-tuning of actin dynamics during neuronal migration and neuritogenesis. Furthermore, Auts2 was expressed in developing mouse and human brain regions such as the frontal cortex, dorsal thalamus, and hippocampus, which have been implicated in the impaired cognitive and social function of ASD. Taken together, a comprehensive understanding of Auts2 functions can give deep insights into the cause of the heterogenous manifestation of neurodevelopmental disorders such as ASD.
The current study examined whether the blind are superior to sighted listeners in voice recognition. Three subject groups, including 17 congenitally blind, 18 late blind, and 18 sighted, showed no significant differences in the immediate voice recognition test. In the delayed test conducted two weeks later, however, both congenitally blind and late blind groups performed better than the sighted with no significant difference between the two blind groups. These results partly confirmed the anecdotal observation about the blind's superiority in voice recognition, which resides mainly in delayed memory phase but not in immediate recall and generalization phase.
Humans recognize one another by identifying their voices and faces. For sighted people, the integration of voice and face signals in corresponding brain networks plays an important role in facilitating the process. However, individuals with vision loss primarily resort to voice cues to recognize a person’s identity. It remains unclear how the neural systems for voice recognition reorganize in the blind. In the present study, we collected behavioral and resting-state fMRI data from 20 early blind (5 females; mean age = 22.6 years) and 22 sighted control (7 females; mean age = 23.7 years) individuals. We aimed to investigate the alterations in the resting-state functional connectivity (FC) among the voice- and face-sensitive areas in blind subjects in comparison with controls. We found that the intranetwork connections among voice-sensitive areas, including amygdala-posterior “temporal voice areas” (TVAp), amygdala-anterior “temporal voice areas” (TVAa), and amygdala-inferior frontal gyrus (IFG) were enhanced in the early blind. The blind group also showed increased FCs of “fusiform face area” (FFA)-IFG and “occipital face area” (OFA)-IFG but decreased FCs between the face-sensitive areas (i.e., FFA and OFA) and TVAa. Moreover, the voice-recognition accuracy was positively related to the strength of TVAp-FFA in the sighted, and the strength of amygdala-FFA in the blind. These findings indicate that visual deprivation shapes functional connectivity by increasing the intranetwork connections among voice-sensitive areas while decreasing the internetwork connections between the voice- and face-sensitive areas. Moreover, the face-sensitive areas are still involved in the voice-recognition process in blind individuals through pathways such as the subcortical-occipital or occipitofrontal connections, which may benefit the visually impaired greatly during voice processing.
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